Inflammation: the link between comorbidities, genetics, and Alzheimer’s disease
Open accessAbstract
Alzheimer's disease (AD) is a neurodegenerative disorder, most cases of which lack a clear causative event. This has made the disease difficult to characterize and, thus, diagnose. Although some cases are genetically linked, there are many diseases and lifestyle factors that can lead to an increased risk of developing AD, including traumatic brain injury, diabetes, hypertension, obesity, and other metabolic syndromes, in addition to aging. Identifying common factors and trends between these conditions could enhance our understanding of AD and lead to the development of more effective treatments. Although the immune system is one of the body's key defense mechanisms, chronic inflammation has been increasingly linked with several age-related diseases. Moreover, it is now well accepted that chronic inflammation has an important role in the onset and progression of AD. In this review, the different inflammatory signals associated with AD and its risk factors will be outlined to demonstrate how chronic inflammation may be influencing individual susceptibility to AD. Our goal is to bring attention to potential shared signals presented by the immune system during different conditions that could lead to the development of successful treatments.
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Disrupted immune function is a potential link between metabolic and neurodegenerative disease states.
“Intriguingly, it has been suggested that disrupted immune function is a potential link between these disease states (Pugazhenthi et al., 2017; Newcombe et al., 2018).”
From Deletion of the Alzheimer’s disease risk gene Abi3 locus results in obesity and systemic metabolic disruption in mice (2022) · cites this paper as Newcombe et al., 2018
Metabolomic biomarkers such as reduced docosahexaenoic acid (DHA) and elevated homocysteine have demonstrated clinical utility.
“Despite variability introduced by diet and comorbid conditions, metabolomic biomarkers such as reduced docosahexaenoic acid (DHA) and elevated homocysteine have demonstrated clinical utility133,194, 195, 196, 197, 198, 199.”
From Artificial intelligence-driven multi-omics approaches in Alzheimer's disease: Progress, challenges, and future directions (2025) · cites this paper as [198]
The section “The metabolic disorders and AD” (page unavailable) discusses diet, metabolic conditions, and inflammation, but not the clinical utility of metabolomic biomarkers. Searches for docosahexaenoic acid, homocysteine, and metabolomic biomarkers found no passage addressing the claimed markers or their clinical utility. (LLM, conf=0.73)
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Amyloid oligomers exacerbate tau pathology in a mouse model of tauopathy
Selenica, M.-L. B., Brownlow, M., Jimenez, J. P., Lee, D. C., Pena, G., Dickey, C. A., Gordon, M. N., & Morgan, D. (2013) · Neurodegenerative Diseases · doi:10.1159/000337230 · Cited by 10,359 · see citing works
Obesity is associated with macrophage accumulation in adipose tissue
Weisberg, S. P., McCann, D., Desai, M., Rosenbaum, M., Leibel, R. L., & Ferrante, A. W. (2003) · Journal of Clinical Investigation · doi:10.1172/jci200319246 · Cited by 10,041 · see citing works
Neurotoxic reactive astrocytes are induced by activated microglia
Liddelow, S. A., Guttenplan, K. A., Clarke, L. E., Bennett, F. C., Bohlen, C. J., Schirmer, L., Bennett, M. L., Münch, A. E., Chung, W.-S., Peterson, T. C., et al. (2017) · Nature · doi:10.1038/nature21029 · Cited by 7,971 · see citing works
A Unique Microglia Type Associated with Restricting Development of Alzheimer’s Disease
Keren-Shaul, H., Spinrad, A., Weiner, A., Matcovitch-Natan, O., Dvir-Szternfeld, R., Ulland, T. K., David, E., Baruch, K., Lara-Astaiso, D., Toth, B., et al. (2017) · Cell · doi:10.1016/j.cell.2017.05.018 · Cited by 5,493 · see citing works
Microglia Sculpt Postnatal Neural Circuits in an Activity and Complement-Dependent Manner
Schafer, D. P., Lehrman, E. K., Kautzman, A. G., Koyama, R., Mardinly, A. R., Yamasaki, R., Ransohoff, R. M., Greenberg, M. E., Barres, B. A., & Stevens, B. (2012) · Neuron · doi:10.1016/j.neuron.2012.03.026 · Cited by 4,089 · see citing works
Complement and microglia mediate early synapse loss in Alzheimer mouse models
Hong, S., Beja-Glasser, V. F., Nfonoyim, B. M., Frouin, A., Li, S., Ramakrishnan, S., Merry, K. M., Shi, Q., Rosenthal, A., Barres, B. A., et al. (2016) · Science · doi:10.1126/science.aad8373 · Cited by 3,343 · see citing works
Krasemann, S., Madore, C., Cialic, R., Baufeld, C., Calcagno, N., El Fatimy, R., Beckers, L., O’Loughlin, E., Xu, Y., Fanek, Z., et al. (2017) · Immunity · doi:10.1016/j.immuni.2017.08.008 · Cited by 2,979 · see citing works
NLRP3 is activated in Alzheimer’s disease and contributes to pathology in APP/PS1 mice
Heneka, M. T., Kummer, M. P., Stutz, A., Delekate, A., Schwartz, S., Vieira-Saecker, A., Griep, A., Axt, D., Remus, A., Tzeng, T.-C., et al. (2013) · Nature · doi:10.1038/nature11729 · Cited by 2,898 · see citing works
Synapse Loss and Microglial Activation Precede Tangles in a P301S Tauopathy Mouse Model
Yoshiyama, Y., Higuchi, M., Zhang, B., Huang, S.-M., Iwata, N., Saido, T. C., Maeda, J., Suhara, T., Trojanowski, J. Q., & Lee, V. M.-Y. (2007) · Neuron · doi:10.1016/j.neuron.2007.01.010 · Cited by 2,208 · see citing works
Blood-brain barrier breakdown in the aging human hippocampus
Montagne, A., Barnes, S. R., Sweeney, M. D., Halliday, M. R., Sagare, A. P., Zhao, Z., Toga, A. W., Jacobs, R. E., Liu, C. Y., Amezcua, L., et al. (2015) · Neuron · doi:10.1016/j.neuron.2014.12.032 · Cited by 2,102 · see citing works
Nelson, P. T., Alafuzoff, I., Bigio, E. H., Bouras, C., Braak, H., Cairns, N. J., Castellani, R. J., Crain, B. J., Davies, P., Tredici, K. D., et al. (2012) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e31825018f7 · Cited by 2,050 · see citing works
RAGE and amyloid-β peptide neurotoxicity in Alzheimer's disease
Yan, S. D., Chen, X., Fu, J., Chen, M., Zhu, H., Roher, A., Slattery, T., Zhao, L., Nagashima, M., Morser, J., et al. (1996) · Nature · doi:10.1038/382685a0 · Cited by 2,012 · see citing works
the Immunological Genome Consortium, Gautier, E. L., Shay, T., Miller, J., Greter, M., Jakubzick, C., Ivanov, S., Helft, J., Chow, A., Elpek, K. G., et al. (2012) · Nature Immunology · doi:10.1038/ni.2419 · Cited by 1,972 · see citing works
Naj, A. C., Jun, G., Beecham, G. W., Wang, L.-S., Vardarajan, B. N., Buros, J., Gallins, P. J., Buxbaum, J. D., Jarvik, G. P., Crane, P. K., et al. (2011) · Nature Genetics · doi:10.1038/ng.801 · Cited by 1,901 · see citing works
Astrocyte scar formation aids central nervous system axon regeneration
Anderson, M. A., Burda, J. E., Ren, Y., Ao, Y., O’Shea, T. M., Kawaguchi, R., Coppola, G., Khakh, B. S., Deming, T. J., & Sofroniew, M. V. (2016) · Nature · doi:10.1038/nature17623 · Cited by 1,851 · see citing works
Microglial Dysfunction and Defective β-Amyloid Clearance Pathways in Aging Alzheimer's Disease Mice
Hickman, S. E., Allison, E. K., & El Khoury, J. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.0616-08.2008 · Cited by 1,329 · see citing works
Copps, K. D., & White, M. F. (2012) · Diabetologia · doi:10.1007/s00125-012-2644-8 · Cited by 1,017 · see citing works
Innate immune memory in the brain shapes neurological disease hallmarks
Wendeln, A.-C., Degenhardt, K., Kaurani, L., Gertig, M., Ulas, T., Jain, G., Wagner, J., Häsler, L. M., Wild, K., Skodras, A., et al. (2018) · Nature · doi:10.1038/s41586-018-0023-4 · Cited by 956 · see citing works
Bacterial infection causes stress-induced memory dysfunction in mice
Gareau, M. G., Wine, E., Rodrigues, D. M., Cho, J. H., Whary, M. T., Philpott, D. J., MacQueen, G., & Sherman, P. M. (2011) · Gut · doi:10.1136/gut.2009.202515 · Cited by 909 · see citing works
TREM2 mutations implicated in neurodegeneration impair cell surface transport and phagocytosis
Kleinberger, G., Yamanishi, Y., Suárez-Calvet, M., Czirr, E., Lohmann, E., Cuyvers, E., Struyfs, H., Pettkus, N., Wenninger-Weinzierl, A., Mazaheri, F., et al. (2014) · Science Translational Medicine · doi:10.1126/scitranslmed.3009093 · Cited by 798 · see citing works
Picomolar Amyloid-β Positively Modulates Synaptic Plasticity and Memory in Hippocampus
Puzzo, D., Privitera, L., Leznik, E., Fà, M., Staniszewski, A., Palmeri, A., & Arancio, O. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.2692-08.2008 · Cited by 740 · see citing works
Regulation of Tau Pathology by the Microglial Fractalkine Receptor
Bhaskar, K., Konerth, M., Kokiko-Cochran, O. N., Cardona, A., Ransohoff, R. M., & Lamb, B. T. (2010) · Neuron · doi:10.1016/j.neuron.2010.08.023 · Cited by 639 · see citing works
Age-related myelin degradation burdens the clearance function of microglia during aging
Safaiyan, S., Kannaiyan, N., Snaidero, N., Brioschi, S., Biber, K., Yona, S., Edinger, A. L., Jung, S., Rossner, M. J., & Simons, M. (2016) · Nature Neuroscience · doi:10.1038/nn.4325 · Cited by 604 · see citing works
A new fate mapping system reveals context-dependent random or clonal expansion of microglia
Tay, T. L., Mai, D., Dautzenberg, J., Fernández-Klett, F., Lin, G., Sagar, Datta, M., Drougard, A., Stempfl, T., Ardura-Fabregat, A., et al. (2017) · Nature Neuroscience · doi:10.1038/nn.4547 · Cited by 597 · see citing works
Complement C3 deficiency protects against neurodegeneration in aged plaque-rich APP/PS1 mice
Shi, Q., Chowdhury, S., Ma, R., Le, K. X., Hong, S., Caldarone, B. J., Stevens, B., & Lemere, C. A. (2017) · Science Translational Medicine · doi:10.1126/scitranslmed.aaf6295 · Cited by 593 · see citing works
Transcranial amelioration of inflammation and cell death after brain injury.
Roth, T. L., Nayak, D., Atanasijevic, T., Koretsky, A. P., Latour, L. L., & McGavern, D. B. (2014) · Nature · doi:10.1038/nature12808 · Cited by 574 · see citing works
CD33 Alzheimer's disease locus: altered monocyte function and amyloid biology
Initiative, T. A. D. N., Bradshaw, E. M., Chibnik, L. B., Keenan, B. T., Ottoboni, L., Raj, T., Tang, A., Rosenkrantz, L. L., Imboywa, S., Lee, M., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3435 · Cited by 570 · see citing works
Alzheimer's disease drug development pipeline: 2017
Cummings, J., Lee, G., Mortsdorf, T., Ritter, A., & Zhong, K. (2017) · Alzheimer's & Dementia: Translational Research & Clinical Interventions · doi:10.1016/j.trci.2017.05.002 · Cited by 549 · see citing works
Lee, S., Varvel, N. H., Konerth, M. E., Xu, G., Cardona, A. E., Ransohoff, R. M., & Lamb, B. T. (2010) · The American Journal of Pathology · doi:10.2353/ajpath.2010.100265 · Cited by 539 · see citing works
Olmos-Alonso, A., Schetters, S. T. T., Sri, S., Askew, K., Mancuso, R., Vargas-Caballero, M., Holscher, C., Perry, V. H., & Gomez-Nicola, D. (2016) · Brain · doi:10.1093/brain/awv379 · Cited by 532 · see citing works
Leyns, C. E. G., Ulrich, J. D., Finn, M. B., Stewart, F. R., Koscal, L. J., Remolina Serrano, J., Robinson, G. O., Anderson, E., Colonna, M., & Holtzman, D. M. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1710311114 · Cited by 517 · see citing works
Cribbs, D. H., Berchtold, N. C., Perreau, V., Coleman, P. D., Rogers, J., Tenner, A. J., & Cotman, C. W. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-179 · Cited by 499 · see citing works
Endothelial LRP1 transports amyloid-β1–42 across the blood-brain barrier
Storck, S. E., Meister, S., Nahrath, J., Meißner, J. N., Schubert, N., Di Spiezio, A., Baches, S., Vandenbroucke, R. E., Bouter, Y., Prikulis, I., et al. (2015) · Journal of Clinical Investigation · doi:10.1172/jci81108 · Cited by 477 · see citing works
Kitazawa, M., Cheng, D., Tsukamoto, M. R., Koike, M. A., Wes, P. D., Vasilevko, V., Cribbs, D. H., & LaFerla, F. M. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1100620 · Cited by 473 · see citing works
Brosseron, F., Krauthausen, M., Kummer, M., & Heneka, M. T. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-8657-1 · Cited by 447 · see citing works
Formation and maintenance of Alzheimer's disease β-amyloid plaques in the absence of microglia
Grathwohl, S. A., Kälin, R. E., Bolmont, T., Prokop, S., Winkelmann, G., Kaeser, S. A., Odenthal, J., Radde, R., Eldh, T., Gandy, S., et al. (2009) · Nature Neuroscience · doi:10.1038/nn.2432 · Cited by 401 · see citing works
Gao, X., Cao, Q., Cheng, Y., Zhao, D., Wang, Z., Yang, H., Wu, Q., You, L., Wang, Y., Lin, Y., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1720696115 · Cited by 400 · see citing works
He, P., Zhong, Z., Lindholm, K., Berning, L., Lee, W., Lemere, C., Staufenbiel, M., Li, R., & Shen, Y. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200705042 · Cited by 390 · see citing works
Lucin, K. M., O’Brien, C. E., Bieri, G., Czirr, E., Mosher, K. I., Abbey, R. J., Mastroeni, D. F., Rogers, J., Spencer, B., Masliah, E., et al. (2013) · Neuron · doi:10.1016/j.neuron.2013.06.046 · Cited by 374 · see citing works
IL-33 ameliorates Alzheimer's disease-like pathology and cognitive decline
Fu, A. K. Y., Hung, K.-W., Yuen, M. Y. F., Zhou, X., Mak, D. S. Y., Chan, I. C. W., Cheung, T. H., Zhang, B., Fu, W.-Y., Liew, F. Y., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1604032113 · Cited by 369 · see citing works
Il10 Deficiency Rebalances Innate Immunity to Mitigate Alzheimer-Like Pathology
Guillot-Sestier, M.-V., Doty, K. R., Gate, D., Rodriguez, J., Leung, B. P., Rezai-Zadeh, K., & Town, T. (2015) · Neuron · doi:10.1016/j.neuron.2014.12.068 · Cited by 363 · see citing works
Semple, B. D., Bye, N., Rancan, M., Ziebell, J. M., & Morganti-Kossmann, M. C. (2010) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2009.262 · Cited by 358 · see citing works
Kang, D. E., Pietrzik, C. U., Baum, L., Chevallier, N., Merriam, D. E., Kounnas, M. Z., Wagner, S. L., Troncoso, J. C., Kawas, C. H., Katzman, R., et al. (2000) · Journal of Clinical Investigation · doi:10.1172/jci11013 · Cited by 354 · see citing works
TREM2 deficiency impairs chemotaxis and microglial responses to neuronal injury
Mazaheri, F., Snaidero, N., Kleinberger, G., Madore, C., Daria, A., Werner, G., Krasemann, S., Capell, A., Trümbach, D., Wurst, W., et al. (2017) · The EMBO Reports · doi:10.15252/embr.201743922 · Cited by 351 · see citing works
Neuroinflammatory TNFα Impairs Memory via Astrocyte Signaling
Habbas, S., Santello, M., Becker, D., Stubbe, H., Zappia, G., Liaudet, N., Klaus, F. R., Kollias, G., Fontana, A., Pryce, C. R., et al. (2015) · Cell · doi:10.1016/j.cell.2015.11.023 · Cited by 347 · see citing works
Biagi, E., Nylund, L., Candela, M., Ostan, R., Bucci, L., Pini, E., Nikkïla, J., Monti, D., Satokari, R., Franceschi, C., et al. (2010) · PLoS ONE · doi:10.1371/annotation/df45912f-d15c-44ab-8312-e7ec0607604d · Cited by 345 · see citing works
Absence of C1q Leads to Less Neuropathology in Transgenic Mouse Models of Alzheimer's Disease
Fonseca, M. I., Zhou, J., Botto, M., & Tenner, A. J. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.0901-04.2004 · Cited by 345 · see citing works
Arai, Y., Martin-Ruiz, C. M., Takayama, M., Abe, Y., Takebayashi, T., Koyasu, S., Suematsu, M., Hirose, N., & von Zglinicki, T. (2015) · EBioMedicine · doi:10.1016/j.ebiom.2015.07.029 · Cited by 333 · see citing works
Increased cerebrospinal fluid soluble TREM2 concentration in Alzheimer’s disease
Heslegrave, A., Heywood, W., Paterson, R., Magdalinou, N., Svensson, J., Johansson, P., Öhrfelt, A., Blennow, K., Hardy, J., Schott, J., et al. (2016) · Molecular Neurodegeneration · doi:10.1186/s13024-016-0071-x · Cited by 303 · see citing works
Pattern Recognition by TREM-2: Binding of Anionic Ligands
Daws, M. R., Sullam, P. M., Niemi, E. C., Chen, T. T., Tchao, N. K., & Seaman, W. E. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.171.2.594 · Cited by 291 · see citing works
Interleukin-1β Induces Blood–Brain Barrier Disruption by Downregulating Sonic Hedgehog in Astrocytes
Wang, Y., Jin, S., Sonobe, Y., Cheng, Y., Horiuchi, H., Parajuli, B., Kawanokuchi, J., Mizuno, T., Takeuchi, H., & Suzumura, A. (2014) · PLoS ONE · doi:10.1371/journal.pone.0110024 · Cited by 286 · see citing works
Neuronal Clearance of Amyloid-β by Endocytic Receptor LRP1
Kanekiyo, T., Cirrito, J. R., Liu, C.-C., Shinohara, M., Li, J., Schuler, D. R., Shinohara, M., Holtzman, D. M., & Bu, G. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.3487-13.2013 · Cited by 280 · see citing works
Liu, Z., Condello, C., Schain, A., Harb, R., & Grutzendler, J. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4403-10.2010 · Cited by 276 · see citing works
Astrocytic LRP1 Mediates Brain Aβ Clearance and Impacts Amyloid Deposition
Liu, C.-C., Hu, J., Zhao, N., Wang, J., Wang, N., Cirrito, J. R., Kanekiyo, T., Holtzman, D. M., & Bu, G. (2017) · The Journal of Neuroscience · doi:10.1523/jneurosci.3442-16.2017 · Cited by 267 · see citing works
Immune aging, dysmetabolism, and inflammation in neurological diseases
Deleidi, M., Jäggle, M., & Rubino, G. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00172 · Cited by 260 · see citing works
Shaftel, S. S., Carlson, T. J., Olschowka, J. A., Kyrkanides, S., Matousek, S. B., & O'Banion, M. K. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.1418-07.2007 · Cited by 243 · see citing works
Wang, T., Hu, X., Liang, S., Li, W., Wu, X., Wang, L., & Jin, F. (2015) · Beneficial Microbes · doi:10.3920/bm2014.0177 · Cited by 233 · see citing works
Microglial repopulation resolves inflammation and promotes brain recovery after injury: RICE et al.
Rice, R. A., Pham, J., Lee, R. J., Najafi, A. R., West, B. L., & Green, K. N. (2017) · Glia · doi:10.1002/glia.23135 · Cited by 228 · see citing works
APOE genotype alters glial activation and loss of synaptic markers in mice
Zhu, Y., Nwabuisi‐Heath, E., Dumanis, S. B., Tai, L. M., Yu, C., Rebeck, G. W., & Ladu, M. J. (2012) · Glia · doi:10.1002/glia.22289 · Cited by 224 · see citing works
Astrocytic tight junctions control inflammatory CNS lesion pathogenesis
Horng, S., Therattil, A., Moyon, S., Gordon, A., Kim, K., Argaw, A. T., Hara, Y., Mariani, J. N., Sawai, S., Flodby, P., et al. (2017) · Journal of Clinical Investigation · doi:10.1172/jci91301 · Cited by 221 · see citing works
Inflammation Induced by Infection Potentiates Tau Pathological Features in Transgenic Mice
Sy, M., Kitazawa, M., Medeiros, R., Whitman, L., Cheng, D., Lane, T. E., & LaFerla, F. M. (2011) · The American Journal of Pathology · doi:10.1016/j.ajpath.2011.02.012 · Cited by 210 · see citing works
Self-citationRevisiting Metchnikoff: Age-related alterations in microbiota-gut-brain axis in the mouse
Scott, K. A., Ida, M., Peterson, V. L., Prenderville, J. A., Moloney, G. M., Izumo, T., Murphy, K., Murphy, A., Ross, R. P., Stanton, C., et al. (2017) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2017.02.004 · Cited by 202 · see citing works
Human APOE4 increases microglia reactivity at Aβ plaques in a mouse model of Aβ deposition
Rodriguez, G. A., Tai, L. M., LaDu, M. J., & Rebeck, G. W. (2014) · Journal of Neuroinflammation · doi:10.1186/1742-2094-11-111 · Cited by 193 · see citing works
Terwel, D., Steffensen, K. R., Verghese, P. B., Kummer, M. P., Gustafsson, J.-Å., Holtzman, D. M., & Heneka, M. T. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.6546-10.2011 · Cited by 181 · see citing works
Kahn, M. S., Kranjac, D., Alonzo, C. A., Haase, J. H., Cedillos, R. O., McLinden, K. A., Boehm, G. W., & Chumley, M. J. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.01.010 · Cited by 177 · see citing works
Castillo, E., Leon, J., Mazzei, G., Abolhassani, N., Haruyama, N., Saito, T., Saido, T., Hokama, M., Iwaki, T., Ohara, T., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-17999-3 · Cited by 158 · see citing works
Accumulation of tau induced in neurites by microglial proinflammatory mediators
Gorlovoy, P., Larionov, S., Pham, T. T. H., & Neumann, H. (2009) · The FASEB Journal · doi:10.1096/fj.08-123877 · Cited by 156 · see citing works
Raj, T., Ryan, K. J., Replogle, J. M., Chibnik, L. B., Rosenkrantz, L., Tang, A., Rothamel, K., Stranger, B. E., Bennett, D. A., Evans, D. A., et al. (2014) · Human Molecular Genetics · doi:10.1093/hmg/ddt666 · Cited by 144 · see citing works
TREM2 promotes Aβ phagocytosis by upregulating C/EBPα-dependent CD36 expression in microglia
Kim, S.-M., Mun, B.-R., Lee, S.-J., Joh, Y., Lee, H.-Y., Ji, K.-Y., Choi, H.-R., Lee, E.-H., Kim, E.-M., Jang, J.-H., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-11634-x · Cited by 143 · see citing works
Haure-Mirande, J.-V., Audrain, M., Fanutza, T., Kim, S. H., Klein, W. L., Glabe, C., Readhead, B., Dudley, J. T., Blitzer, R. D., Wang, M., et al. (2017) · Acta Neuropathologica · doi:10.1007/s00401-017-1737-3 · Cited by 127 · see citing works
Microglial complement receptor 3 regulates brain Aβ levels through secreted proteolytic activity
Czirr, E., Castello, N. A., Mosher, K. I., Castellano, J. M., Hinkson, I. V., Lucin, K. M., Baeza-Raja, B., Ryu, J. K., Li, L., Farina, S. N., et al. (2017) · Journal of Experimental Medicine · doi:10.1084/jem.20162011 · Cited by 126 · see citing works
Loss of tau rescues inflammation-mediated neurodegeneration
Maphis, N., Xu, G., Kokiko-Cochran, O. N., Cardona, A. E., Ransohoff, R. M., Lamb, B. T., & Bhaskar, K. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00196 · Cited by 91 · see citing works
Spampinato, S. F., Merlo, S., Sano, Y., Kanda, T., & Sortino, M. A. (2017) · Journal of Neurochemistry · doi:10.1111/jnc.14068 · Cited by 90 · see citing works
MHC class I modulates NMDA receptor function and AMPA receptor trafficking
Fourgeaud, L., Davenport, C. M., Tyler, C. M., Cheng, T. T., Spencer, M. B., & Boulanger, L. M. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0914064107 · Cited by 89 · see citing works
Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer’s disease
On behalf of the European Early-Onset Dementia (EU EOD) consortium, De Roeck, A., Van den Bossche, T., van der Zee, J., Verheijen, J., De Coster, W., Van Dongen, J., Dillen, L., Baradaran-Heravi, Y., Heeman, B., et al. (2017) · Acta Neuropathologica · doi:10.1007/s00401-017-1714-x · Cited by 74 · see citing works
Aging alters mRNA expression of amyloid transporter genes at the blood-brain barrier
Osgood, D., Miller, M. C., Messier, A. A., Gonzalez, L., & Silverberg, G. D. (2017) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2017.05.011 · Cited by 63 · see citing works
Increased ATP-binding cassette transporter A1 expression in Alzheimer's disease hippocampal neurons
Kim, W. S., Bhatia, S., Elliott, D. A., Agholme, L., Kågedal, K., McCann, H., Halliday, G. M., Barnham, K. J., & Garner, B. (2010) · Journal of Alzheimer's Disease · doi:10.3233/jad-2010-100324 · Cited by 40 · see citing works
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Research works printed but not linked: 243
- [2]Fullerton JN Gilroy DW Resolution of inflammation: a new therapeutic frontier Nat Rev Drug Discov 2016 15 8 551 567 10.1038/nrd.2016.39 27020098 · DOI · Paper page
- [4]Grabert K Michoel T Karavolos MH Clohisey S Baillie JK Stevens MP Microglial brain region-dependent diversity and selective regional sensitivities to aging Nat Neurosci 2016 19 3 504 516 10.1038/nn.4222 26780511 PMC4768346 · DOI · Paper page
- [5]Askew K Li K Olmos-Alonso A Garcia-Moreno F Liang Y Richardson P Coupled proliferation and apoptosis maintain the rapid turnover of microglia in the adult brain Cell Rep 2017 18 2 391 405 10.1016/j.celrep.2016.12.041 28076784 PMC5263237 · DOI · Paper page
- [6]Zamanian JL Xu L Foo LC Nouri N Zhou L Giffard RG Genomic analysis of reactive astrogliosis J Neurosci 2012 32 18 6391 6410 10.1523/JNEUROSCI.6221-11.2012 22553043 PMC3480225 · DOI · Paper page
- [7]Livne-Bar I Wei J Liu HH Alqawlaq S Won GJ Tuccitto A Astrocyte-derived lipoxins A4 and B4 promote neuroprotection from acute and chronic injury J Clin Invest 2017 127 12 4403 4414 10.1172/JCI77398 29106385 PMC5707141 · DOI
- [8]Vainchtein ID Chin G Cho FS Kelley KW Miller JG Chien EC Astrocyte-derived interleukin-33 promotes microglial synapse engulfment and neural circuit development Science 2018 359 6381 1269 1273 10.1126/science.aal3589 29420261 PMC6070131 · DOI · Paper page
- [13]Galatro TF Holtman IR Lerario AM Vainchtein ID Brouwer N Sola PR Transcriptomic analysis of purified human cortical microglia reveals age-associated changes Nat Neurosci 2017 20 8 1162 1171 10.1038/nn.4597 28671693 · DOI · Paper page
- [14]Streit WJ Sammons NW Kuhns AJ Sparks DL Dystrophic microglia in the aging human brain Glia 2004 45 2 208 212 10.1002/glia.10319 14730714 · DOI · Paper page
- [15]Mrdjen D Pavlovic A Hartmann FJ Schreiner B Utz SG Leung BP High-dimensional single-cell mapping of central nervous system immune cells reveals distinct myeloid subsets in health, aging, and disease Immunity 2018 48 2 380 95 e6 10.1016/j.immuni.2018.01.011 29426702 · DOI · Paper page
- [16]Ritzel RM Patel AR Pan S Crapser J Hammond M Jellison E Age- and location-related changes in microglial function Neurobiol Aging 2015 36 6 2153 2163 10.1016/j.neurobiolaging.2015.02.016 25816747 · DOI · Paper page
- [17]Vukovic J Colditz MJ Blackmore DG Ruitenberg MJ Bartlett PF Microglia modulate hippocampal neural precursor activity in response to exercise and aging J Neurosci 2012 32 19 6435 6443 10.1523/JNEUROSCI.5925-11.2012 22573666 PMC6621117 · DOI · Paper page
- [19]Njie EG Boelen E Stassen FR Steinbusch HW Borchelt DR Streit WJ Ex vivo cultures of microglia from young and aged rodent brain reveal age-related changes in microglial function Neurobiol Aging 2012 33 1 195 e1 195 12 10.1016/j.neurobiolaging.2010.05.008 PMC4162517 20580465 · DOI · Paper page
- [20]Bliederhaeuser C Grozdanov V Speidel A Zondler L Ruf WP Bayer H Age-dependent defects of alpha-synuclein oligomer uptake in microglia and monocytes Acta Neuropathol 2016 131 3 379 391 10.1007/s00401-015-1504-2 26576561 · DOI
- [21]Rawji KS Kappen J Tang W Teo W Plemel JR Stys PK Deficient surveillance and phagocytic activity of myeloid cells within demyelinated lesions in aging mice visualized by ex vivo live multiphoton imaging J Neurosci 2018 38 8 1973 1988 29363580 PMC6705888
- [24]Walker KA Hoogeveen RC Folsom AR Ballantyne CM Knopman DS Windham BG Midlife systemic inflammatory markers are associated with late-life brain volume: the ARIC study Neurology 2017 89 22 2262 2270 10.1212/WNL.0000000000004688 29093073 PMC5705246 · DOI · Paper page
- [25]Takechi R Lam V Brook E Giles C Fimognari N Mooranian A Blood-brain barrier dysfunction precedes cognitive decline and neurodegeneration in diabetic insulin resistant mouse model: an implication for causal link Front Aging Neurosci 2017 9 399 10.3389/fnagi.2017.00399 29249964 PMC5717019 · DOI
- [26]Villeda SA Luo J Mosher KI Zou B Britschgi M Bieri G The ageing systemic milieu negatively regulates neurogenesis and cognitive function Nature 2011 477 7362 90 94 10.1038/nature10357 21886162 PMC3170097 · DOI · Paper page
- [28]Elahy M Jackaman C Mamo JC Lam V Dhaliwal SS Giles C Blood-brain barrier dysfunction developed during normal aging is associated with inflammation and loss of tight junctions but not with leukocyte recruitment Immun Ageing 2015 12 2 10.1186/s12979-015-0029-9 25784952 PMC4362825 · DOI · Paper page
- [29]Bell RD Winkler EA Sagare AP Singh I LaRue B Deane R Pericytes control key neurovascular functions and neuronal phenotype in the adult brain and during brain aging Neuron 2010 68 3 409 427 10.1016/j.neuron.2010.09.043 21040844 PMC3056408 · DOI · Paper page
- [30]Orre M Kamphuis W Osborn LM Melief J Kooijman L Huitinga I Acute isolation and transcriptome characterization of cortical astrocytes and microglia from young and aged mice Neurobiol Aging 2014 35 1 1 14 10.1016/j.neurobiolaging.2013.07.008 23954174 · DOI
- [31]Clarke LE Liddelow SA Chakraborty C Munch AE Heiman M Barres BA Normal aging induces A1-like astrocyte reactivity Proc Natl Acad Sci U S A 2018 115 8 E1896 EE905 10.1073/pnas.1800165115 29437957 PMC5828643 · DOI · Paper page
- [33]Alvarez JI Dodelet-Devillers A Kebir H Ifergan I Fabre PJ Terouz S The hedgehog pathway promotes blood-brain barrier integrity and CNS immune quiescence Science 2011 334 6063 1727 1731 10.1126/science.1206936 22144466 · DOI · Paper page
- [35]Liddelow SA Barres BA Reactive astrocytes: production, function, and therapeutic potential Immunity 2017 46 6 957 967 10.1016/j.immuni.2017.06.006 28636962 · DOI · Paper page
- [36]Fuger P Hefendehl JK Veeraraghavalu K Wendeln AC Schlosser C Obermuller U Microglia turnover with aging and in an Alzheimer’s model via long-term in vivo single-cell imaging Nat Neurosci 2017 20 10 1371 1376 10.1038/nn.4631 28846081 · DOI · Paper page
- [39]Liu S Liu Y Hao W Wolf L Kiliaan AJ Penke B TLR2 is a primary receptor for Alzheimer's amyloid beta peptide to trigger neuroinflammatory activation J Immunol 2012 188 3 1098 1107 10.4049/jimmunol.1101121 22198949 · DOI · Paper page
- [40]Deane R Du Yan S Submamaryan RK LaRue B Jovanovic S Hogg E RAGE mediates amyloid-beta peptide transport across the blood-brain barrier and accumulation in brain Nat Med 2003 9 7 907 913 10.1038/nm890 12808450 · DOI · Paper page
- [42]Medeiros R Prediger RD Passos GF Pandolfo P Duarte FS Franco JL Connecting TNF-alpha signaling pathways to iNOS expression in a mouse model of Alzheimer's disease: relevance for the behavioral and synaptic deficits induced by amyloid beta protein J Neurosci 2007 27 20 5394 5404 10.1523/JNEUROSCI.5047-06.2007 17507561 PMC6672347 · DOI · Paper page
- [43]Bonaiuto C McDonald PP Rossi F Cassatella MA Activation of nuclear factor-kappa B by beta-amyloid peptides and interferon-gamma in murine microglia J Neuroimmunol 1997 77 1 51 56 10.1016/S0165-5728(97)00054-4 9209268 · DOI
- [44]Medeiros R Figueiredo CP Pandolfo P Duarte FS Prediger RD Passos GF The role of TNF-alpha signaling pathway on COX-2 upregulation and cognitive decline induced by beta-amyloid peptide Behav Brain Res 2010 209 1 165 173 10.1016/j.bbr.2010.01.040 20122965 · DOI · Paper page
- [45]Soscia SJ Kirby JE Washicosky KJ Tucker SM Ingelsson M Hyman B The Alzheimer’s disease-associated amyloid beta-protein is an antimicrobial peptide PLoS One 2010 5 3 e9505 10.1371/journal.pone.0009505 20209079 PMC2831066 · DOI · Paper page
- [46]Grilli M Ribola M Alberici A Valerio A Memo M Spano P Identification and characterization of a kappa B/Rel binding site in the regulatory region of the amyloid precursor protein gene J Biol Chem 1995 270 45 26774 26777 10.1074/jbc.270.45.26774 7592914 · DOI
- [47]Bourne KZ Ferrari DC Lange-Dohna C Rossner S Wood TG Perez-Polo JR Differential regulation of BACE1 promoter activity by nuclear factor-kappaB in neurons and glia upon exposure to beta-amyloid peptides J Neurosci Res 2007 85 6 1194 1204 10.1002/jnr.21252 17385716 · DOI
- [48]Cho HJ Kim SK Jin SM Hwang EM Kim YS Huh K IFN-gamma-induced BACE1 expression is mediated by activation of JAK2 and ERK1/2 signaling pathways and direct binding of STAT1 to BACE1 promoter in astrocytes Glia 2007 55 3 253 262 10.1002/glia.20451 17091494 · DOI
- [49]Sastre M Dewachter I Rossner S Bogdanovic N Rosen E Borghgraef P Nonsteroidal anti-inflammatory drugs repress beta-secretase gene promoter activity by the activation of PPARgamma Proc Natl Acad Sci U S A 2006 103 2 443 448 10.1073/pnas.0503839103 16407166 PMC1326151 · DOI · Paper page
- [50]Chami L Buggia-Prevot V Duplan E Del Prete D Chami M Peyron JF Nuclear factor-kappaB regulates betaAPP and beta- and gamma-secretases differently at physiological and supraphysiological Abeta concentrations J Biol Chem 2012 287 29 24573 24584 10.1074/jbc.M111.333054 22654105 PMC3397882 · DOI
- [51]Hong HS Hwang EM Sim HJ Cho HJ Boo JH Oh SS Interferon gamma stimulates beta-secretase expression and sAPPbeta production in astrocytes Biochem Biophys Res Commun 2003 307 4 922 927 10.1016/S0006-291X(03)01270-1 12878199 · DOI · Paper page
- [53]Yang H Zhuo JM Chu J Chinnici C Pratico D Amelioration of the Alzheimer's disease phenotype by absence of 12/15-lipoxygenase Biol Psychiatry 2010 68 10 922 929 10.1016/j.biopsych.2010.04.010 20570249 · DOI
- [54]Varga T Czimmerer Z Nagy L PPARs are a unique set of fatty acid regulated transcription factors controlling both lipid metabolism and inflammation Biochim Biophys Acta 2011 1812 8 1007 1022 10.1016/j.bbadis.2011.02.014 21382489 PMC3117990 · DOI · Paper page
- [55]Katsouri L Lim YM Blondrath K Eleftheriadou I Lombardero L Birch AM PPARgamma-coactivator-1alpha gene transfer reduces neuronal loss and amyloid-beta generation by reducing beta-secretase in an Alzheimer’s disease model Proc Natl Acad Sci U S A 2016 113 43 12292 12297 10.1073/pnas.1606171113 27791018 PMC5087021 · DOI · Paper page
- [56]Chu J Pratico D The 5-lipoxygenase as modulator of Alzheimer’s gamma-secretase and therapeutic target Brain Res Bull 2016 126 Pt 2 207 212 10.1016/j.brainresbull.2016.03.010 27005438 PMC5028246 · DOI
- [57]Lu B Figini M Emanueli C Geppetti P Grady EF Gerard NP The control of microvascular permeability and blood pressure by neutral endopeptidase Nat Med 1997 3 8 904 907 10.1038/nm0897-904 9256283 · DOI
- [58]Sturiale S Barbara G Qiu B Figini M Geppetti P Gerard N Neutral endopeptidase (EC 3.4.24.11) terminates colitis by degrading substance P Proc Natl Acad Sci U S A 1999 96 20 11653 11658 10.1073/pnas.96.20.11653 10500232 PMC18089 · DOI
- [59]Kirkwood KS Bunnett NW Maa J Castagliolo I Liu B Gerard N Deletion of neutral endopeptidase exacerbates intestinal inflammation induced by Clostridium difficile toxin A Am J Physiol Gastrointest Liver Physiol 2001 281 2 G544 G551 10.1152/ajpgi.2001.281.2.G544 11447035 · DOI
- [60]Scholzen TE Steinhoff M Bonaccorsi P Klein R Amadesi S Geppetti P Neutral endopeptidase terminates substance P-induced inflammation in allergic contact dermatitis J Immunol 2001 166 2 1285 1291 10.4049/jimmunol.166.2.1285 11145711 · DOI
- [61]Kong Y Ruan L Qian L Liu X Le Y Norepinephrine promotes microglia to uptake and degrade amyloid beta peptide through upregulation of mouse formyl peptide receptor 2 and induction of insulin-degrading enzyme J Neurosci 2010 30 35 11848 11857 10.1523/JNEUROSCI.2985-10.2010 20810904 PMC6633413 · DOI
- [63]Ren M Guo Q Guo L Lenz M Qian F Koenen RR Polymerization of MIP-1 chemokine (CCL3 and CCL4) and clearance of MIP-1 by insulin-degrading enzyme EMBO J 2010 29 23 3952 3966 10.1038/emboj.2010.256 20959807 PMC3020635 · DOI
- [64]Hellstrom-Lindahl E Ravid R Nordberg A Age-dependent decline of neprilysin in Alzheimer's disease and normal brain: inverse correlation with A beta levels Neurobiol Aging 2008 29 2 210 221 10.1016/j.neurobiolaging.2006.10.010 17098332 · DOI
- [65]Zhao Z Xiang Z Haroutunian V Buxbaum JD Stetka B Pasinetti GM Insulin degrading enzyme activity selectively decreases in the hippocampal formation of cases at high risk to develop Alzheimer’s disease Neurobiol Aging 2007 28 6 824 830 10.1016/j.neurobiolaging.2006.05.001 16769157 · DOI
- [69]Fernandez-Castaneda A Arandjelovic S Stiles TL Schlobach RK Mowen KA Gonias SL Identification of the low density lipoprotein (LDL) receptor-related protein-1 interactome in central nervous system myelin suggests a role in the clearance of necrotic cell debris J Biol Chem 2013 288 7 4538 4548 10.1074/jbc.M112.384693 23264627 PMC3576060 · DOI
- [70]Chuang TY Guo Y Seki SM Rosen AM Johanson DM Mandell JW LRP1 expression in microglia is protective during CNS autoimmunity Acta Neuropathol Commun. 2016 4 1 68 10.1186/s40478-016-0343-2 27400748 PMC4940960 · DOI
- [71]Mantuano E Brifault C Lam MS Azmoon P Gilder AS Gonias SL LDL receptor-related protein-1 regulates NFkappaB and microRNA-155 in macrophages to control the inflammatory response Proc Natl Acad Sci U S A 2016 113 5 1369 1374 10.1073/pnas.1515480113 26787872 PMC4747752 · DOI
- [72]Yang L Liu CC Zheng H Kanekiyo T Atagi Y Jia L LRP1 modulates the microglial immune response via regulation of JNK and NF-kappaB signaling pathways J Neuroinflammation 2016 13 1 304 10.1186/s12974-016-0772-7 27931217 PMC5146875 · DOI
- [75]Steinberg S Stefansson H Jonsson T Johannsdottir H Ingason A Helgason H Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease Nat Genet 2015 47 5 445 447 10.1038/ng.3246 25807283 · DOI · Paper page
- [77]Karasinska JM de Haan W Franciosi S Ruddle P Fan J Kruit JK ABCA1 influences neuroinflammation and neuronal death Neurobiol Dis 2013 54 445 455 10.1016/j.nbd.2013.01.018 23376685 · DOI · Paper page
- [78]Jehle AW Gardai SJ Li S Linsel-Nitschke P Morimoto K Janssen WJ ATP-binding cassette transporter A7 enhances phagocytosis of apoptotic cells and associated ERK signaling in macrophages J Cell Biol 2006 174 4 547 556 10.1083/jcb.200601030 16908670 PMC2064260 · DOI
- [79]Morizawa YM Hirayama Y Ohno N Shibata S Shigetomi E Sui Y Reactive astrocytes function as phagocytes after brain ischemia via ABCA1-mediated pathway Nat Commun 2017 8 1 28 10.1038/s41467-017-00037-1 28642575 PMC5481424 · DOI
- [80]Fu Y Hsiao JH Paxinos G Halliday GM Kim WS ABCA7 mediates phagocytic clearance of amyloid-beta in the brain J Alzheimers Dis 2016 54 2 569 584 10.3233/JAD-160456 27472885 · DOI
- [82]Vasquez JB Fardo DW Estus S ABCA7 expression is associated with Alzheimer’s disease polymorphism and disease status Neurosci Lett 2013 556 58 62 10.1016/j.neulet.2013.09.058 24141082 PMC3863933 · DOI · Paper page
- [85]Thakker DR Sankaranarayanan S Weatherspoon MR Harrison J Pierdomenico M Heisel JM Centrally delivered BACE1 inhibitor activates microglia, and reverses amyloid pathology and cognitive deficit in aged Tg2576 mice J Neurosci 2015 35 17 6931 6936 10.1523/JNEUROSCI.2262-14.2015 25926467 PMC6605183 · DOI
- [86]Streit WJ Braak H Xue QS Bechmann I Dystrophic (senescent) rather than activated microglial cells are associated with tau pathology and likely precede neurodegeneration in Alzheimer’s disease Acta Neuropathol 2009 118 4 475 485 10.1007/s00401-009-0556-6 19513731 PMC2737117 · DOI · Paper page
- [87]Brawek B Schwendele B Riester K Kohsaka S Lerdkrai C Liang Y Impairment of in vivo calcium signaling in amyloid plaque-associated microglia Acta Neuropathol 2014 127 4 495 505 10.1007/s00401-013-1242-2 24407428 · DOI
- [89]Fan Z Brooks DJ Okello A Edison P An early and late peak in microglial activation in Alzheimer’s disease trajectory Brain 2017 140 3 792 803 28122877 PMC5837520
- [91]Seabrook TJ Jiang L Maier M Lemere CA Minocycline affects microglia activation, Abeta deposition, and behavior in APP-tg mice Glia 2006 53 7 776 782 10.1002/glia.20338 16534778 · DOI
- [94]Dagher NN Najafi AR Kayala KM Elmore MR White TE Medeiros R Colony-stimulating factor 1 receptor inhibition prevents microglial plaque association and improves cognition in 3xTg-AD mice J Neuroinflammation 2015 12 139 10.1186/s12974-015-0366-9 26232154 PMC4522109 · DOI · Paper page
- [95]Spangenberg EE Lee RJ Najafi AR Rice RA Elmore MR Blurton-Jones M Eliminating microglia in Alzheimer’s mice prevents neuronal loss without modulating amyloid-beta pathology Brain 2016 139 Pt 4 1265 1281 10.1093/brain/aww016 26921617 PMC5006229 · DOI · Paper page
- [97]Fuhrmann M Bittner T Jung CK Burgold S Page RM Mitteregger G Microglial Cx3cr1 knockout prevents neuron loss in a mouse model of Alzheimer’s disease Nat Neurosci 2010 13 4 411 413 10.1038/nn.2511 20305648 PMC4072212 · DOI · Paper page
- [103]Hernandez MX Jiang S Cole TA Chu SH Fonseca MI Fang MJ Prevention of C5aR1 signaling delays microglial inflammatory polarization, favors clearance pathways and suppresses cognitive loss Mol Neurodegener 2017 12 1 66 10.1186/s13024-017-0210-z 28923083 PMC5604420 · DOI
- [104]Liu Y Liu X Hao W Decker Y Schomburg R Fulop L IKKbeta deficiency in myeloid cells ameliorates Alzheimer’s disease-related symptoms and pathology J Neurosci 2014 34 39 12982 12999 10.1523/JNEUROSCI.1348-14.2014 25253847 PMC6608331 · DOI
- [105]Michaud JP Halle M Lampron A Theriault P Prefontaine P Filali M Toll-like receptor 4 stimulation with the detoxified ligand monophosphoryl lipid A improves Alzheimer’s disease-related pathology Proc Natl Acad Sci U S A 2013 110 5 1941 1946 10.1073/pnas.1215165110 23322736 PMC3562771 · DOI
- [106]Cluff CW Monophosphoryl lipid A (MPL) as an adjuvant for anti-cancer vaccines: clinical results Adv Exp Med Biol 2010 667 111 123 10.1007/978-1-4419-1603-7_10 20665204 · DOI
- [108]Chakrabarty P Li A Ceballos-Diaz C Eddy JA Funk CC Moore B IL-10 alters immunoproteostasis in APP mice, increasing plaque burden and worsening cognitive behavior Neuron 2015 85 3 519 533 10.1016/j.neuron.2014.11.020 25619653 PMC4320003 · DOI · Paper page
- [109]Medeiros R Kitazawa M Passos GF Baglietto-Vargas D Cheng D Cribbs DH Aspirin-triggered lipoxin A4 stimulates alternative activation of microglia and reduces Alzheimer disease-like pathology in mice Am J Pathol 2013 182 5 1780 1789 10.1016/j.ajpath.2013.01.051 23506847 PMC3644736 · DOI · Paper page
- [110]Dunn HC Ager RR Baglietto-Vargas D Cheng D Kitazawa M Cribbs DH Restoration of lipoxin A4 signaling reduces Alzheimer's disease-like pathology in the 3xTg-AD mouse model J Alzheimers Dis 2015 43 3 893 903 10.3233/JAD-141335 25125468 PMC4319708 · DOI
- [111]Woodling NS Wang Q Priyam PG Larkin P Shi J Johansson JU Suppression of Alzheimer-associated inflammation by microglial prostaglandin-E2 EP4 receptor signaling J Neurosci 2014 34 17 5882 5894 10.1523/JNEUROSCI.0410-14.2014 24760848 PMC3996215 · DOI
- [113]Wang X Zhu M Hjorth E Cortes-Toro V Eyjolfsdottir H Graff C Resolution of inflammation is altered in Alzheimer’s disease Alzheimers Dement 2015 11 1 40 50 e1–2 10.1016/j.jalz.2013.12.024 24530025 PMC4275415 · DOI · Paper page
- [114]Marin I Kipnis J Learning and memory... and the immune system Learn Mem 2013 20 10 601 606 10.1101/lm.028357.112 24051097 PMC3768198 · DOI · Paper page
- [115]Kitazawa M Oddo S Yamasaki TR Green KN LaFerla FM Lipopolysaccharide-induced inflammation exacerbates tau pathology by a cyclin-dependent kinase 5-mediated pathway in a transgenic model of Alzheimer’s disease J Neurosci 2005 25 39 8843 8853 10.1523/JNEUROSCI.2868-05.2005 16192374 PMC6725603 · DOI · Paper page
- [116]Kitazawa M Trinh DN LaFerla FM Inflammation induces tau pathology in inclusion body myositis model via glycogen synthase kinase-3beta Ann Neurol 2008 64 1 15 24 10.1002/ana.21325 18318434 · DOI
- [118]Maphis N Xu G Kokiko-Cochran ON Jiang S Cardona A Ransohoff RM Reactive microglia drive tau pathology and contribute to the spreading of pathological tau in the brain Brain 2015 138 Pt 6 1738 1755 10.1093/brain/awv081 25833819 PMC4542622 · DOI · Paper page
- [119]Sanchez-Mejias E Navarro V Jimenez S Sanchez-Mico M Sanchez-Varo R Nunez-Diaz C Soluble phospho-tau from Alzheimer’s disease hippocampus drives microglial degeneration Acta Neuropathol 2016 132 6 897 916 10.1007/s00401-016-1630-5 27743026 PMC5106501 · DOI · Paper page
- [122]Asai H Ikezu S Tsunoda S Medalla M Luebke J Haydar T Depletion of microglia and inhibition of exosome synthesis halt tau propagation Nat Neurosci 2015 18 11 1584 1593 10.1038/nn.4132 26436904 PMC4694577 · DOI · Paper page
- [124]Noble W Garwood C Stephenson J Kinsey AM Hanger DP Anderton BH Minocycline reduces the development of abnormal tau species in models of Alzheimer’s disease FASEB J 2009 23 3 739 750 10.1096/fj.08-113795 19001528 · DOI
- [125]Hunt JB Jr Nash KR Placides D Moran P Selenica ML Abuqalbeen F Sustained arginase 1 expression modulates pathological tau deposits in a mouse model of tauopathy J Neurosci 2015 35 44 14842 14860 10.1523/JNEUROSCI.3959-14.2015 26538654 PMC6605229 · DOI
- [126]Roe AD Staup MA Serrats J Sawchenko PE Rissman RA Lipopolysaccharide-induced tau phosphorylation and kinase activity--modulation, but not mediation, by corticotropin-releasing factor receptors Eur J Neurosci 2011 34 3 448 456 10.1111/j.1460-9568.2011.07764.x 21722209 PMC3148267 · DOI
- [127]Lee DC Rizer J Selenica ML Reid P Kraft C Johnson A LPS- induced inflammation exacerbates phospho-tau pathology in rTg4510 mice J Neuroinflammation 2010 7 56 10.1186/1742-2094-7-56 20846376 PMC2949628 · DOI · Paper page
- [129]Piras A Collin L Gruninger F Graff C Ronnback A Autophagic and lysosomal defects in human tauopathies: analysis of post-mortem brain from patients with familial Alzheimer disease, corticobasal degeneration and progressive supranuclear palsy Acta Neuropathol Commun 2016 4 22 10.1186/s40478-016-0292-9 26936765 PMC4774096 · DOI · Paper page
- [131]Cho SH Chen JA Sayed F Ward ME Gao F Nguyen TA SIRT1 deficiency in microglia contributes to cognitive decline in aging and neurodegeneration via epigenetic regulation of IL-1beta J Neurosci 2015 35 2 807 818 10.1523/JNEUROSCI.2939-14.2015 25589773 PMC4293425 · DOI · Paper page
- [132]Ghosh S Wu MD Shaftel SS Kyrkanides S LaFerla FM Olschowka JA Sustained interleukin-1beta overexpression exacerbates tau pathology despite reduced amyloid burden in an Alzheimer's mouse model J Neurosci 2013 33 11 5053 5064 10.1523/JNEUROSCI.4361-12.2013 23486975 PMC3637949 · DOI · Paper page
- [134]Lee S Xu G Jay TR Bhatta S Kim KW Jung S Opposing effects of membrane-anchored CX3CL1 on amyloid and tau pathologies via the p38 MAPK pathway J Neurosci 2014 34 37 12538 12546 10.1523/JNEUROSCI.0853-14.2014 25209291 PMC4160782 · DOI · Paper page
- [135]Petkau TL Leavitt BR Progranulin in neurodegenerative disease Trends Neurosci 2014 37 7 388 398 10.1016/j.tins.2014.04.003 24800652 · DOI
- [136]Takahashi H Klein ZA Bhagat SM Kaufman AC Kostylev MA Ikezu T Opposing effects of progranulin deficiency on amyloid and tau pathologies via microglial TYROBP network Acta Neuropathol 2017 133 5 785 807 10.1007/s00401-017-1668-z 28070672 PMC5391267 · DOI
- [138]Goddard CA Butts DA Shatz CJ Regulation of CNS synapses by neuronal MHC class I Proc Natl Acad Sci U S A 2007 104 16 6828 6833 10.1073/pnas.0702023104 17420446 PMC1871870 · DOI · Paper page
- [139]Lazarczyk MJ Kemmler JE Eyford BA Short JA Varghese M Sowa A Major histocompatibility complex class I proteins are critical for maintaining neuronal structural complexity in the aging brain Sci Rep 2016 6 26199 10.1038/srep26199 27229916 PMC4882527 · DOI · Paper page
- [141]Prieto GA, Tong L, Smith ED, Cotman CW. TNFalpha and IL-1beta but not IL-18 suppresses hippocampal long-term potentiation directly at the synapse. Neurochem Res. 2018; 10.1007/s11064-018-2517-8. [Epub ahead of print] PMC6170724 29619614 · DOI
- [142]Prieto GA Snigdha S Baglietto-Vargas D Smith ED Berchtold NC Tong L Synapse-specific IL-1 receptor subunit reconfiguration augments vulnerability to IL-1beta in the aged hippocampus Proc Natl Acad Sci U S A 2015 112 36 E5078 E5087 10.1073/pnas.1514486112 26305968 PMC4568670 · DOI · Paper page
- [143]Parkhurst CN Yang G Ninan I Savas JN Yates JR 3rd Lafaille JJ Microglia promote learning-dependent synapse formation through brain-derived neurotrophic factor Cell 2013 155 7 1596 1609 10.1016/j.cell.2013.11.030 24360280 PMC4033691 · DOI · Paper page
- [144]Zhan Y Paolicelli RC Sforazzini F Weinhard L Bolasco G Pagani F Deficient neuron-microglia signaling results in impaired functional brain connectivity and social behavior Nat Neurosci 2014 17 3 400 406 10.1038/nn.3641 24487234 · DOI · Paper page
- [148]Ma J Choi BR Chung C Min SS Jeon WK Han JS Chronic brain inflammation causes a reduction in GluN2A and GluN2B subunits of NMDA receptors and an increase in the phosphorylation of mitogen-activated protein kinases in the hippocampus Mol Brain 2014 7 33 10.1186/1756-6606-7-33 24761931 PMC4021635 · DOI
- [149]Liu Y Xu X Dou H Hua Y Xu J Hui X Apolipoprotein E knockout induced inflammatory responses related to microglia in neonatal mice brain via astrocytes Int J Clin Exp Med 2015 8 1 737 743 25785051 PMC4358506
- [150]Sheng H Laskowitz DT Mackensen GB Kudo M Pearlstein RD Warner DS Apolipoprotein E deficiency worsens outcome from global cerebral ischemia in the mouse Stroke 1999 30 5 1118 1124 10.1161/01.STR.30.5.1118 10229753 · DOI
- [151]Lynch JR Pineda JA Morgan D Zhang L Warner DS Benveniste H Apolipoprotein E affects the central nervous system response to injury and the development of cerebral edema Ann Neurol 2002 51 1 113 117 10.1002/ana.10098 11782990 · DOI · Paper page
- [152]Lynch JR Morgan D Mance J Matthew WD Laskowitz DT Apolipoprotein E modulates glial activation and the endogenous central nervous system inflammatory response J Neuroimmunol 2001 114 1–2 107 113 10.1016/S0165-5728(00)00459-8 11240021 · DOI
- [153]Guo L LaDu MJ Van Eldik LJ A dual role for apolipoprotein e in neuroinflammation: anti- and pro-inflammatory activity J Mol Neurosci 2004 23 3 205 212 10.1385/JMN:23:3:205 15181248 · DOI · Paper page
- [154]Vitek MP Brown CM Colton CA APOE genotype-specific differences in the innate immune response Neurobiol Aging 2009 30 9 1350 1360 10.1016/j.neurobiolaging.2007.11.014 18155324 PMC2782461 · DOI · Paper page
- [157]den Hartigh LJ Altman R Hutchinson R Petrlova J Budamagunta MS Tetali SD Postprandial apoE isoform and conformational changes associated with VLDL lipolysis products modulate monocyte inflammation PLoS One 2012 7 11 e50513 10.1371/journal.pone.0050513 23209766 PMC3509065 · DOI
- [158]Gale SC, Gao L, Mikacenic C, Coyle SM, Rafaels N, Murray Dudenkov T, et al. APOepsilon4 is associated with enhanced in vivo innate immune responses in human subjects. J Allergy Clin Immunol. 2014;134(1):127–34. PMC4125509 24655576
- [159]Lynch JR Tang W Wang H Vitek MP Bennett ER Sullivan PM APOE genotype and an ApoE-mimetic peptide modify the systemic and central nervous system inflammatory response J Biol Chem 2003 278 49 48529 48533 10.1074/jbc.M306923200 14507923 · DOI · Paper page
- [160]Maezawa I Zaja-Milatovic S Milatovic D Stephen C Sokal I Maeda N Apolipoprotein E isoform-dependent dendritic recovery of hippocampal neurons following activation of innate immunity J Neuroinflammation 2006 3 21 10.1186/1742-2094-3-21 16934151 PMC1584222 · DOI
- [161]Rodriguez GA Burns MP Weeber EJ Rebeck GW Young APOE4 targeted replacement mice exhibit poor spatial learning and memory, with reduced dendritic spine density in the medial entorhinal cortex Learn Mem 2013 20 5 256 266 10.1101/lm.030031.112 23592036 PMC3630489 · DOI
- [163]Atagi Y Liu CC Painter MM Chen XF Verbeeck C Zheng H Apolipoprotein E is a ligand for triggering receptor expressed on myeloid cells 2 (TREM2) J Biol Chem 2015 290 43 26043 26050 10.1074/jbc.M115.679043 26374899 PMC4646257 · DOI · Paper page
- [165]Guerreiro R Wojtas A Bras J Carrasquillo M Rogaeva E Majounie E TREM2 variants in Alzheimer's disease N Engl J Med 2013 368 2 117 127 10.1056/NEJMoa1211851 23150934 PMC3631573 · DOI · Paper page
- [166]Cruchaga C Kauwe JS Harari O Jin SC Cai Y Karch CM GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer’s disease Neuron 2013 78 2 256 268 10.1016/j.neuron.2013.02.026 23562540 PMC3664945 · DOI · Paper page
- [169]Kobayashi M Konishi H Sayo A Takai T Kiyama H TREM2/DAP12 signal elicits proinflammatory response in microglia and exacerbates neuropathic pain J Neurosci 2016 36 43 11138 11150 10.1523/JNEUROSCI.1238-16.2016 27798193 PMC6705657 · DOI
- [170]Zhao Y Wu X Li X Jiang LL Gui X Liu Y TREM2 is a receptor for beta-amyloid that mediates microglial function Neuron 2018 97 5 1023 1031 10.1016/j.neuron.2018.01.031 29518356 PMC5889092 · DOI · Paper page
- [171]Bouchon A Hernandez-Munain C Cella M Colonna M A DAP12-mediated pathway regulates expression of CC chemokine receptor 7 and maturation of human dendritic cells J Exp Med 2001 194 8 1111 1122 10.1084/jem.194.8.1111 11602640 PMC2193511 · DOI · Paper page
- [172]Ito H Hamerman JA TREM-2, triggering receptor expressed on myeloid cell-2, negatively regulates TLR responses in dendritic cells Eur J Immunol 2012 42 1 176 185 10.1002/eji.201141679 21956652 PMC3444819 · DOI · Paper page
- [173]Zhong L Chen XF Wang T Wang Z Liao C Wang Z Soluble TREM2 induces inflammatory responses and enhances microglial survival J Exp Med 2017 214 3 597 607 28209725 PMC5339672
- [175]Suarez-Calvet M Kleinberger G Araque Caballero MA Brendel M Rominger A Alcolea D sTREM2 cerebrospinal fluid levels are a potential biomarker for microglia activity in early-stage Alzheimer’s disease and associate with neuronal injury markers EMBO Mol Med 2016 8 5 466 476 10.15252/emmm.201506123 26941262 PMC5120370 · DOI · Paper page
- [176]Kober DL, Alexander-Brett JM, Karch CM, Cruchaga C, Colonna M, Holtzman MJ, et al. Neurodegenerative disease mutations in TREM2 reveal a functional surface and distinct loss-of-function mechanisms. elife. 2016;5:e20391. PMC5173322 27995897
- [177]Jonsson T Stefansson H Steinberg S Jonsdottir I Jonsson PV Snaedal J Variant of TREM2 associated with the risk of Alzheimer’s disease N Engl J Med 2013 368 2 107 116 10.1056/NEJMoa1211103 23150908 PMC3677583 · DOI · Paper page
- [179]Cheng Qingwen Danao Jean Talreja Santosh Wen Paul Yin Jun Sun Ning Li Chi-Ming Chui Danny Tran David Koirala Samir Chen Hang Foltz Ian N. Wang Songli Sambashivan Shilpa TREM2-activating antibodies abrogate the negative pleiotropic effects of the Alzheimer's disease variantTrem2R47Hon murine myeloid cell function Journal of Biological Chemistry 2018 293 32 12620 12633 10.1074/jbc.RA118.001848 29599291 PMC6093249 · DOI
- [180]Yeh FL Wang Y Tom I Gonzalez LC Sheng M TREM2 binds to apolipoproteins, including APOE and CLU/APOJ, and thereby facilitates uptake of amyloid-Beta by microglia Neuron 2016 91 2 328 340 10.1016/j.neuron.2016.06.015 27477018 · DOI · Paper page
- [181]Jay TR Hirsch AM Broihier ML Miller CM Neilson LE Ransohoff RM Disease progression-dependent effects of TREM2 deficiency in a mouse model of Alzheimer’s disease J Neurosci 2017 37 3 637 647 10.1523/JNEUROSCI.2110-16.2016 28100745 PMC5242410 · DOI · Paper page
- [182]Jiang T Tan L Zhu XC Zhang QQ Cao L Tan MS Upregulation of TREM2 ameliorates neuropathology and rescues spatial cognitive impairment in a transgenic mouse model of Alzheimer’s disease Neuropsychopharmacology 2014 39 13 2949 2962 10.1038/npp.2014.164 25047746 PMC4229581 · DOI · Paper page
- [185]Hamerman JA Jarjoura JR Humphrey MB Nakamura MC Seaman WE Lanier LL Cutting edge: inhibition of TLR and FcR responses in macrophages by triggering receptor expressed on myeloid cells (TREM)-2 and DAP12 J Immunol 2006 177 4 2051 2055 10.4049/jimmunol.177.4.2051 16887962 · DOI · Paper page
- [186]Bemiller SM McCray TJ Allan K Formica SV Xu G Wilson G TREM2 deficiency exacerbates tau pathology through dysregulated kinase signaling in a mouse model of tauopathy Mol Neurodegener 2017 12 1 74 10.1186/s13024-017-0216-6 29037207 PMC5644120 · DOI · Paper page
- [188]Jiang Teng Zhang Ying-Dong Gao Qing Ou Zhou Gong Peng-Yu Shi Jian-Quan Wu Liang Zhou Jun-Shan TREM2 Ameliorates Neuronal Tau Pathology Through Suppression of Microglial Inflammatory Response Inflammation 2018 41 3 811 823 10.1007/s10753-018-0735-5 29362997 · DOI
- [189]Ulyanova T Blasioli J Woodford-Thomas TA Thomas ML The sialoadhesin CD33 is a myeloid-specific inhibitory receptor Eur J Immunol 1999 29 11 3440 3449 10.1002/(SICI)1521-4141(199911)29:11<3440::AID-IMMU3440>3.0.CO;2-C 10556798 · DOI
- [190]Lajaunias F Dayer JM Chizzolini C Constitutive repressor activity of CD33 on human monocytes requires sialic acid recognition and phosphoinositide 3-kinase-mediated intracellular signaling Eur J Immunol 2005 35 1 243 251 10.1002/eji.200425273 15597323 · DOI
- [191]Gonzalez Y Herrera MT Soldevila G Garcia-Garcia L Fabian G Perez-Armendariz EM High glucose concentrations induce TNF-alpha production through the down-regulation of CD33 in primary human monocytes BMC Immunol 2012 13 19 10.1186/1471-2172-13-19 22500980 PMC3353220 · DOI
- [192]Bertram L Lange C Mullin K Parkinson M Hsiao M Hogan MF Genome-wide association analysis reveals putative Alzheimer’s disease susceptibility loci in addition to APOE Am J Hum Genet 2008 83 5 623 632 10.1016/j.ajhg.2008.10.008 18976728 PMC2668052 · DOI · Paper page
- [193]Karch CM Jeng AT Nowotny P Cady J Cruchaga C Goate AM Expression of novel Alzheimer's disease risk genes in control and Alzheimer’s disease brains PLoS One 2012 7 11 e50976 10.1371/journal.pone.0050976 23226438 PMC3511432 · DOI · Paper page
- [197]Malik M Simpson JF Parikh I Wilfred BR Fardo DW Nelson PT CD33 Alzheimer’s risk-altering polymorphism, CD33 expression, and exon 2 splicing J Neurosci 2013 33 33 13320 13325 10.1523/JNEUROSCI.1224-13.2013 23946390 PMC3742922 · DOI · Paper page
- [198]Griciuc A Serrano-Pozo A Parrado AR Lesinski AN Asselin CN Mullin K Alzheimer’s disease risk gene CD33 inhibits microglial uptake of amyloid beta Neuron 2013 78 4 631 643 10.1016/j.neuron.2013.04.014 23623698 PMC3706457 · DOI · Paper page
- [199]Walker DG Whetzel AM Serrano G Sue LI Beach TG Lue LF Association of CD33 polymorphism rs3865444 with Alzheimer’s disease pathology and CD33 expression in human cerebral cortex Neurobiol Aging 2015 36 2 571 582 10.1016/j.neurobiolaging.2014.09.023 25448602 PMC4315751 · DOI · Paper page
- [200]Chan G White CC Winn PA Cimpean M Replogle JM Glick LR CD33 modulates TREM2: convergence of Alzheimer loci Nat Neurosci 2015 18 11 1556 1558 10.1038/nn.4126 26414614 PMC4682915 · DOI · Paper page
- [201]Caldeira C Cunha C Vaz AR Falcao AS Barateiro A Seixas E Key aging-associated alterations in primary microglia response to Beta-amyloid stimulation Front Aging Neurosci 2017 9 277 10.3389/fnagi.2017.00277 28912710 PMC5583148 · DOI · Paper page
- [202]Walker JM Harrison FE Shared neuropathological characteristics of obesity, type 2 diabetes and Alzheimer’s disease: impacts on cognitive decline Nutrients 2015 7 9 7332 7357 10.3390/nu7095341 26340637 PMC4586536 · DOI
- [203]Arvanitakis Z Wilson RS Bienias JL Evans DA Bennett DA Diabetes mellitus and risk of Alzheimer disease and decline in cognitive function Arch Neurol 2004 61 5 661 666 10.1001/archneur.61.5.661 15148141 · DOI · Paper page
- [204]Li JQ Tan L Wang HF Tan MS Tan L Xu W Risk factors for predicting progression from mild cognitive impairment to Alzheimer's disease: a systematic review and meta-analysis of cohort studies J Neurol Neurosurg Psychiatry 2016 87 5 476 484 10.1136/jnnp-2014-310095 26001840 · DOI
- [205]Yamamoto N Matsubara T Sobue K Tanida M Kasahara R Naruse K Brain insulin resistance accelerates Abeta fibrillogenesis by inducing GM1 ganglioside clustering in the presynaptic membranes J Neurochem 2012 121 4 619 628 10.1111/j.1471-4159.2012.07668.x 22260232 · DOI
- [206]Stanley M Macauley SL Caesar EE Koscal LJ Moritz W Robinson GO The effects of peripheral and central high insulin on brain insulin signaling and amyloid-beta in young and old APP/PS1 mice J Neurosci 2016 36 46 11704 11715 10.1523/JNEUROSCI.2119-16.2016 27852778 PMC5125227 · DOI
- [207]Farris W Mansourian S Chang Y Lindsley L Eckman EA Frosch MP Insulin-degrading enzyme regulates the levels of insulin, amyloid beta-protein, and the beta-amyloid precursor protein intracellular domain in vivo Proc Natl Acad Sci U S A 2003 100 7 4162 4167 10.1073/pnas.0230450100 12634421 PMC153065 · DOI
- [208]Kim B Figueroa-Romero C Pacut C Backus C Feldman EL Insulin resistance prevents AMPK-induced tau dephosphorylation through Akt-mediated increase in AMPKSer-485 phosphorylation J Biol Chem 2015 290 31 19146 19157 10.1074/jbc.M115.636852 26100639 PMC4521037 · DOI
- [209]Spolcova A Mikulaskova B Krskova K Gajdosechova L Zorad S Olszanecki R Deficient hippocampal insulin signaling and augmented tau phosphorylation is related to obesity- and age-induced peripheral insulin resistance: a study in Zucker rats BMC Neurosci 2014 15 111 10.1186/1471-2202-15-111 25257559 PMC4261609 · DOI
- [210]Park S Kim DS Kang S Moon NR Beta-amyloid-induced cognitive dysfunction impairs glucose homeostasis by increasing insulin resistance and decreasing beta-cell mass in non-diabetic and diabetic rats Metabolism 2013 62 12 1749 1760 10.1016/j.metabol.2013.08.007 24050268 · DOI
- [211]Moser V. Alexandra Pike Christian J. Obesity Accelerates Alzheimer-Related Pathology in APOE4 but not APOE3 Mice eneuro 2017 4 3 ENEURO.0077-17.2017 10.1523/ENEURO.0077-17.2017 28612048 PMC5469027 · DOI
- [212]Johnson LA, Torres ER, Weber Boutros S, Patel E, Akinyeke T, Alkayed NJ, et al. Apolipoprotein E4 mediates insulin resistance-associated cerebrovascular dysfunction and the post-prandial response. J Cereb Blood Flow Metab. 2017;1:271678X17746186. PMC6498752 29215310
- [213]Mustain WC Starr ME Valentino JD Cohen DA Okamura D Wang C Inflammatory cytokine gene expression in mesenteric adipose tissue during acute experimental colitis PLoS One 2013 8 12 e83693 10.1371/journal.pone.0083693 24386254 PMC3873328 · DOI
- [214]Haghani K Pashaei S Vakili S Taheripak G Bakhtiyari S TNF-alpha knockdown alleviates palmitate-induced insulin resistance in C2C12 skeletal muscle cells Biochem Biophys Res Commun 2015 460 4 977 982 10.1016/j.bbrc.2015.03.137 25839650 · DOI
- [216]Cortez M Carmo LS Rogero MM Borelli P Fock RA A high-fat diet increases IL-1, IL-6, and TNF-alpha production by increasing NF-kappaB and attenuating PPAR-gamma expression in bone marrow mesenchymal stem cells Inflammation 2013 36 2 379 386 10.1007/s10753-012-9557-z 23079940 · DOI
- [217]Lukic L Lalic NM Rajkovic N Jotic A Lalic K Milicic T Hypertension in obese type 2 diabetes patients is associated with increases in insulin resistance and IL-6 cytokine levels: potential targets for an efficient preventive intervention Int J Environ Res Public Health 2014 11 4 3586 3598 10.3390/ijerph110403586 24686488 PMC4025026 · DOI
- [218]van der Heijden RA Sheedfar F Morrison MC Hommelberg PP Kor D Kloosterhuis NJ High-fat diet induced obesity primes inflammation in adipose tissue prior to liver in C57BL/6j mice Aging (Albany NY) 2015 7 4 256 268 10.18632/aging.100738 25979814 PMC4429090 · DOI
- [219]Gao M Ma Y Liu D High-fat diet-induced adiposity, adipose inflammation, hepatic steatosis and hyperinsulinemia in outbred CD-1 mice PLoS One 2015 10 3 e0119784 10.1371/journal.pone.0119784 25768847 PMC4358885 · DOI
- [220]Lee HM Kim JJ Kim HJ Shong M Ku BJ Jo EK Upregulated NLRP3 inflammasome activation in patients with type 2 diabetes Diabetes 2013 62 1 194 204 10.2337/db12-0420 23086037 PMC3526026 · DOI
- [221]McKie EA Reid JL Mistry PC DeWall SL Abberley L Ambery PD A study to investigate the efficacy and safety of an anti-Interleukin-18 monoclonal antibody in the treatment of type 2 diabetes mellitus PLoS One 2016 11 3 e0150018 10.1371/journal.pone.0150018 26930607 PMC4773233 · DOI
- [222]Lenart N Brough D Denes A Inflammasomes link vascular disease with neuroinflammation and brain disorders J Cereb Blood Flow Metab 2016 36 10 1668 1685 10.1177/0271678X16662043 27486046 PMC5076791 · DOI
- [223]Hou HW Petchakup C Tay HM Tam ZY Dalan R Chew DE Rapid and label-free microfluidic neutrophil purification and phenotyping in diabetes mellitus Sci Rep 2016 6 29410 10.1038/srep29410 27381673 PMC4933935 · DOI
- [224]Horvath P Oliver SR Ganesan G Zaldivar FP Jr Radom-Aizik S Galassetti PR Fasting glucose level modulates cell surface expression of CD11b and CD66b in granulocytes and monocytes of patients with type 2 diabetes J Investig Med 2013 61 6 972 977 10.2310/JIM.0b013e3182961517 23686079 PMC3738167 · DOI
- [225]Dasu MR Jialal I Free fatty acids in the presence of high glucose amplify monocyte inflammation via toll-like receptors Am J Physiol Endocrinol Metab 2011 300 1 E145 E154 10.1152/ajpendo.00490.2010 20959532 PMC3023203 · DOI
- [226]Gupta S Maratha A Siednienko J Natarajan A Gajanayake T Hoashi S Analysis of inflammatory cytokine and TLR expression levels in type 2 diabetes with complications Sci Rep 2017 7 1 7633 10.1038/s41598-017-07230-8 28794498 PMC5550417 · DOI
- [228]Chen L Chen R Wang H Liang F Mechanisms linking inflammation to insulin resistance Int J Endocrinol 2015 2015 508409 26136779 PMC4468292
- [229]Koenen TB Stienstra R van Tits LJ de Graaf J Stalenhoef AF Joosten LA Hyperglycemia activates caspase-1 and TXNIP-mediated IL-1beta transcription in human adipose tissue Diabetes 2011 60 2 517 524 10.2337/db10-0266 21270263 PMC3028351 · DOI
- [230]Su D Coudriet GM Hyun Kim D Lu Y Perdomo G Qu S FoxO1 links insulin resistance to proinflammatory cytokine IL-1beta production in macrophages Diabetes 2009 58 11 2624 2633 10.2337/db09-0232 19651810 PMC2768186 · DOI
- [231]Dhande I Ma W Hussain T Angiotensin AT2 receptor stimulation is anti-inflammatory in lipopolysaccharide-activated THP-1 macrophages via increased interleukin-10 production Hypertens Res 2015 38 1 21 29 10.1038/hr.2014.132 25209104 PMC4898267 · DOI
- [232]Feinkohl I Keller M Robertson CM Morling JR McLachlan S Frier BM Cardiovascular risk factors and cognitive decline in older people with type 2 diabetes Diabetologia 2015 58 7 1637 1645 10.1007/s00125-015-3581-0 25847351 PMC4473016 · DOI
- [233]Feinkohl I Keller M Robertson CM Morling JR Williamson RM Nee LD Clinical and subclinical macrovascular disease as predictors of cognitive decline in older patients with type 2 diabetes: the Edinburgh Type 2 Diabetes Study Diabetes Care 2013 36 9 2779 2786 10.2337/dc12-2241 23579182 PMC3747922 · DOI · Paper page
- [234]Umegaki H Kawamura T Umemura T Kawano N Factors associated with cognitive decline in older adults with type 2 diabetes mellitus during a 6-year observation Geriatr Gerontol Int 2015 15 3 302 310 10.1111/ggi.12273 24597930 · DOI
- [235]van Bussel FC Backes WH Hofman PA Puts NA Edden RA van Boxtel MP Increased GABA concentrations in type 2 diabetes mellitus are related to lower cognitive functioning Medicine (Baltimore) 2016 95 36 e4803 10.1097/MD.0000000000004803 27603392 PMC5023915 · DOI
- [236]Tucsek Zsuzsanna Noa Valcarcel-Ares M. Tarantini Stefano Yabluchanskiy Andriy Fülöp Gábor Gautam Tripti Orock Albert Csiszar Anna Deak Ferenc Ungvari Zoltan Hypertension-induced synapse loss and impairment in synaptic plasticity in the mouse hippocampus mimics the aging phenotype: implications for the pathogenesis of vascular cognitive impairment GeroScience 2017 39 4 385 406 10.1007/s11357-017-9981-y PMC5636782 28664509 · DOI
- [237]Bocarsly ME Fasolino M Kane GA LaMarca EA Kirschen GW Karatsoreos IN Obesity diminishes synaptic markers, alters microglial morphology, and impairs cognitive function Proc Natl Acad Sci U S A 2015 112 51 15731 15736 26644559 PMC4697408
- [238]Hao S Dey A Yu X Stranahan AM Dietary obesity reversibly induces synaptic stripping by microglia and impairs hippocampal plasticity Brain Behav Immun 2016 51 230 239 10.1016/j.bbi.2015.08.023 26336035 PMC4679537 · DOI
- [239]Faden AI Loane DJ Chronic neurodegeneration after traumatic brain injury: Alzheimer disease, chronic traumatic encephalopathy, or persistent neuroinflammation? Neurotherapeutics 2015 12 1 143 150 10.1007/s13311-014-0319-5 25421001 PMC4322076 · DOI · Paper page
- [240]Dams-O'Connor K Guetta G Hahn-Ketter AE Fedor A Traumatic brain injury as a risk factor for Alzheimer’s disease: current knowledge and future directions Neurodegener Dis Manag 2016 6 5 417 429 10.2217/nmt-2016-0017 27599555 PMC5066138 · DOI
- [241]DeKosky ST Abrahamson EE Ciallella JR Paljug WR Wisniewski SR Clark RS Association of increased cortical soluble abeta42 levels with diffuse plaques after severe brain injury in humans Arch Neurol 2007 64 4 541 544 10.1001/archneur.64.4.541 17420316 · DOI · Paper page
- [242]Gentleman SM Greenberg BD Savage MJ Noori M Newman SJ Roberts GW A beta 42 is the predominant form of amyloid beta-protein in the brains of short-term survivors of head injury Neuroreport 1997 8 6 1519 1522 10.1097/00001756-199704140-00039 9172166 · DOI
- [243]Johnson VE Stewart W Smith DH Widespread tau and amyloid-beta pathology many years after a single traumatic brain injury in humans Brain Pathol 2012 22 2 142 149 10.1111/j.1750-3639.2011.00513.x 21714827 PMC3979351 · DOI · Paper page
- [244]Acosta SA Tajiri N Sanberg PR Kaneko Y Borlongan CV Increased amyloid precursor protein and tau expression manifests as key secondary cell death in chronic traumatic brain injury J Cell Physiol 2017 232 3 665 677 10.1002/jcp.25629 27699791 PMC5484295 · DOI
- [245]Corrigan F Vink R Blumbergs PC Masters CL Cappai R van den Heuvel C Characterisation of the effect of knockout of the amyloid precursor protein on outcome following mild traumatic brain injury Brain Res 2012 1451 87 99 10.1016/j.brainres.2012.02.045 22424792 · DOI
- [246]Thornton E Vink R Blumbergs PC Van Den Heuvel C Soluble amyloid precursor protein alpha reduces neuronal injury and improves functional outcome following diffuse traumatic brain injury in rats Brain Res 2006 1094 1 38 46 10.1016/j.brainres.2006.03.107 16697978 · DOI
- [247]Plummer S Van den Heuvel C Thornton E Corrigan F Cappai R The neuroprotective properties of the amyloid precursor protein following traumatic brain injury Aging Dis 2016 7 2 163 179 10.14336/AD.2015.0907 27114849 PMC4809608 · DOI
- [249]Corps KN Roth TL McGavern DB Inflammation and neuroprotection in traumatic brain injury JAMA Neurol 2015 72 3 355 362 10.1001/jamaneurol.2014.3558 25599342 PMC5001842 · DOI · Paper page
- [250]Das M Mohapatra S Mohapatra SS New perspectives on central and peripheral immune responses to acute traumatic brain injury J Neuroinflammation 2012 9 236 10.1186/1742-2094-9-236 23061919 PMC3526406 · DOI
- [251]Hinson HE Rowell S Schreiber M Clinical evidence of inflammation driving secondary brain injury: a systematic review J Trauma Acute Care Surg 2015 78 1 184 191 10.1097/TA.0000000000000468 25539220 PMC4297199 · DOI
- [252]Gao H Han Z Bai R Huang S Ge X Chen F The accumulation of brain injury leads to severe neuropathological and neurobehavioral changes after repetitive mild traumatic brain injury Brain Res 2017 1657 1 8 10.1016/j.brainres.2016.11.028 27923640 · DOI
- [253]Liu HD Li W Chen ZR Hu YC Zhang DD Shen W Expression of the NLRP3 inflammasome in cerebral cortex after traumatic brain injury in a rat model Neurochem Res 2013 38 10 2072 2083 10.1007/s11064-013-1115-z 23892989 · DOI
- [254]Gorina R Font-Nieves M Marquez-Kisinousky L Santalucia T Planas AM Astrocyte TLR4 activation induces a proinflammatory environment through the interplay between MyD88-dependent NFkappaB signaling, MAPK, and Jak1/Stat1 pathways Glia 2011 59 2 242 255 10.1002/glia.21094 21125645 · DOI
- [255]Jayakumar AR Tong XY Ruiz-Cordero R Bregy A Bethea JR Bramlett HM Activation of NF-kappaB mediates astrocyte swelling and brain edema in traumatic brain injury J Neurotrauma 2014 31 14 1249 1257 10.1089/neu.2013.3169 24471369 PMC4108982 · DOI
- [256]Hayakawa K Pham LD Katusic ZS Arai K Lo EH Astrocytic high-mobility group box 1 promotes endothelial progenitor cell-mediated neurovascular remodeling during stroke recovery Proc Natl Acad Sci U S A 2012 109 19 7505 7510 10.1073/pnas.1121146109 22529378 PMC3358881 · DOI
- [257]Argaw AT Gurfein BT Zhang Y Zameer A John GR VEGF-mediated disruption of endothelial CLN-5 promotes blood-brain barrier breakdown Proc Natl Acad Sci U S A 2009 106 6 1977 1982 10.1073/pnas.0808698106 19174516 PMC2644149 · DOI · Paper page
- [258]Mark KS Miller DW Increased permeability of primary cultured brain microvessel endothelial cell monolayers following TNF-alpha exposure Life Sci 1999 64 21 1941 1953 10.1016/S0024-3205(99)00139-3 10353592 · DOI
- [259]Wojciak-Stothard B Entwistle A Garg R Ridley AJ Regulation of TNF-alpha-induced reorganization of the actin cytoskeleton and cell-cell junctions by rho, Rac, and Cdc42 in human endothelial cells J Cell Physiol 1998 176 1 150 165 10.1002/(SICI)1097-4652(199807)176:1<150::AID-JCP17>3.0.CO;2-B 9618155 · DOI
- [261]Semple BD Bye N Ziebell JM Morganti-Kossmann MC Deficiency of the chemokine receptor CXCR2 attenuates neutrophil infiltration and cortical damage following closed head injury Neurobiol Dis 2010 40 2 394 403 10.1016/j.nbd.2010.06.015 20621186 · DOI
- [263]Huang J Li Y Tang Y Tang G Yang GY Wang Y CXCR4 antagonist AMD3100 protects blood-brain barrier integrity and reduces inflammatory response after focal ischemia in mice Stroke 2013 44 1 190 197 10.1161/STROKEAHA.112.670299 23168453 · DOI
- [264]Kong LL Wang ZY Hu JF Yuan YH Li H Chen NH Inhibition of chemokine-like factor 1 improves blood-brain barrier dysfunction in rats following focal cerebral ischemia Neurosci Lett 2016 627 192 198 10.1016/j.neulet.2016.06.003 27283776 · DOI
- [265]Szmydynger-Chodobska J Fox LM Lynch KM Zink BJ Chodobski A Vasopressin amplifies the production of proinflammatory mediators in traumatic brain injury J Neurotrauma 2010 27 8 1449 1461 10.1089/neu.2010.1331 20504162 PMC2967824 · DOI
- [266]Mirabelli-Badenier M Braunersreuther V Viviani GL Dallegri F Quercioli A Veneselli E CC and CXC chemokines are pivotal mediators of cerebral injury in ischaemic stroke Thromb Haemost 2011 105 3 409 420 10.1160/TH10-10-0662 21174009 · DOI
- [267]Kenne E Erlandsson A Lindbom L Hillered L Clausen F Neutrophil depletion reduces edema formation and tissue loss following traumatic brain injury in mice J Neuroinflammation 2012 9 17 10.1186/1742-2094-9-17 22269349 PMC3292978 · DOI
- [268]Makinde HM Cuda CM Just TB Perlman HR Schwulst SJ Nonclassical monocytes mediate secondary injury, neurocognitive outcome, and neutrophil infiltration after traumatic brain injury J Immunol 2017 199 10 3583 3591 10.4049/jimmunol.1700896 28993515 PMC5679470 · DOI
- [269]Nagata K Browne KD Suto Y Kumasaka K Cognetti J Johnson VE Early heparin administration after traumatic brain injury: prolonged cognitive recovery associated with reduced cerebral edema and neutrophil sequestration J Trauma Acute Care Surg 2017 83 3 406 412 10.1097/TA.0000000000001590 28538627 PMC9351989 · DOI
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Mithaiwala, M. N., Santana-Coelho, D., Porter, G. A., & O’Connor, J. C. (2021) · Cells · doi:10.3390/cells10061548 · Cited by 190 · see citing works
Inflammatory pathways in Alzheimer’s disease mediated by gut microbiota
Qian, X.-H., Song, X.-X., Liu, X.-L., Chen, S.-D., & Tang, H.-D. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101317 · Cited by 153 · see citing works
Alzheimer’s Disease, Inflammation, and the Role of Antioxidants
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Alzheimer’s Disease and Inflammaging
Kosyreva, A., Sentyabreva, A., Tsvetkov, I., & Makarova, O. (2022) · Brain Sciences · doi:10.3390/brainsci12091237 · Cited by 98 · see citing works
Ren, F., Wei, J., Chen, Q., Hu, M., Yu, L., Mi, J., Zhou, X., Qin, D., Wu, J., & Wu, A. (2025) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2025.07.030 · Cited by 97 · see citing works
Zhang, B., Chen, T., Cao, M., Yuan, C., Reiter, R. J., Zhao, Z., Zhao, Y., Chen, L., Fan, W., Wang, X., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.900132 · Cited by 80 · see citing works
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Cullen, N. C., Mälarstig, A. N., Stomrud, E., Hansson, O., & Mattsson-Carlgren, N. (2021) · Scientific Reports · doi:10.1038/s41598-021-81705-7 · Cited by 62 · see citing works
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Le, L. T. M., Thompson, J. R., Dehghani‐Ghahnaviyeh, S., Pant, S., Dang, P. X., French, J. B., Kanikeyo, T., Tajkhorshid, E., & Alam, A. (2023) · The EMBO Journal · doi:10.15252/embj.2022111065 · Cited by 31 · see citing works
Liu, J., Lin, Y., Yang, Y., Guo, Y., Shang, Y., Zhou, B., Liu, T., Fan, J., & Wei, C. (2022) · Biochemical Pharmacology · doi:10.1016/j.bcp.2022.115149 · Cited by 12 · see citing works
Smith, D. C., Karahan, H., Wijeratne, H. R. S., Al-Amin, M., McCord, B., Moon, Y., & Kim, J. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.1035572 · Cited by 8 · see citing works
“Intriguingly, it has been suggested that disrupted immune function is a potential link between these disease states (Pugazhenthi et al., 2017; Newcombe et al., 2018).”
Background
- Authors
- Newcombe, E. A., Camats-Perna, J., Silva, M. L., Valmas, N., Huat, T. J., & Medeiros, R.
- Affiliations
- The University of Queensland (AU)
- Corresponding author
- Newcombe, Estella A.
- Medeiros, Rodrigo
- Venue
- Journal of Neuroinflammation
- Published
- 2018-09-24
- Volume
- 15
- Issue
- 1
- Pages
- 276-276
- ISSN
- 1742-2094 (ISSN-L)
- PMC
- PMC6154824
- OpenAlex
- W2891379852
- Cited by
- 532
- References
- 77
- Citations by year
- 2026: 29 · 2025: 52 · 2024: 80 · 2023: 84 · 2022: 96 · 2021: 95 · 2020: 65 · 2019: 29 · 2018: 1
- FWCI
- 4.49
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Journal of Neuroinflammation (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, other-oa)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Funders
- National Health and Medical Research Council (GNT1128436, GNT1129192, GNT1139469)
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Keywords
- Alzheimer's disease, chronic inflammation, comorbidities, genetic susceptibility, traumatic brain injury, diabetes mellitus, hypertension, obesity, metabolic syndrome, aging, neuroinflammation, immune system, risk factors, neurodegeneration
- MeSH terms
- Aging, Alzheimer Disease, Astrocytes, Brain, Humans, Inflammation, Neurons
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