Dystrophic microglia are associated with neurodegenerative disease and not healthy aging in the human brain
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Abstract
Abstract Microglia activation—typically described in terms of hypertrophic appearance—is a well-established feature of aging. Recent studies have suggested that microglia dystrophy, not activation, may increase the propagation of progressive neurodegenerative diseases such as Alzheimer’s disease (AD). Yet, a clear understanding of cause and consequences of dystrophic microglia is lacking. Although frequently observed in diseased brains, the appearance of dystrophic microglia in the hippocampus of individuals free of cognitive impairment suggests that microglia may be undergoing senescence with age, leading to dystrophy. Therefore, we hypothesized that chronological age could be a significant contributor to the presence of dystrophic microglia. To investigate this relationship, we employed stereological counts of total microglia, hypertrophic, and dystrophic microglia across the decades of the human lifespan. The microglia counts were performed in the frontal cortex gray and white matter and the CA1 subregion of the hippocampus in individuals without known neurodegenerative disease. There was age-associated increase in the number of dystrophic microglia in the CA1 region and the frontal cortex gray matter related to age. However, the increase in dystrophic microglia was proportional to the age-related increase in the total number of microglia, suggesting that aging alone was not sufficient to explain the presence of dystrophic microglia. We next tested if dystrophic microglia could be a disease-associated microglia phenotype. Compared to controls without neuropathology, the number of dystrophic microglia was significantly greater in aged-matched cases with either AD, dementia with Lewy bodies, or LATE-NC. These results provide evidence that healthy aging is only associated with a modest increase in dystrophic microglia and suggest that dystrophic microglia may be a disease-associated microglia phenotype. Finally, we found strong evidence for iron homeostasis changes, with increases in ferritin light chain, in dystrophic microglia compared to ramified or hypertrophic microglia. Based on our findings, microglia dystrophy, and not hypertrophic microglia, are the disease-associated microglia morphology. Future work is required to understand the links between the increase in dystrophic microglia and neurodegenerative disorders.
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Increased ferritin accumulation in human microglia in ND but not old age has been suggested, and altered iron homeostasis has been proposed as a distinguishing factor between aged 'healthy' microglia and those associated with neurodegeneration.
“One study by Shahidehpour et al. suggests that there is increased ferritin accumulation in human microglia in ND but not old age, and proposed altered iron homeostasis as a distinguishing factor between aged ‘healthy’ microglia and those associated with neurodegeneration [132].”
From Untangling senescent and damage‐associated microglia in the aging and diseased brain (2023) · cites this paper as [132]
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López-Otín, C., Blasco, M. A., Partridge, L., Serrano, M., & Kroemer, G. (2013) · Cell · doi:10.1016/j.cell.2013.05.039 · Cited by 14,982 · 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
Cellular Senescence: Defining a Path Forward
Gorgoulis, V., Adams, P. D., Alimonti, A., Bennett, D. C., Bischof, O., Bishop, C., Campisi, J., Collado, M., Evangelou, K., Ferbeyre, G., et al. (2019) · Cell · doi:10.1016/j.cell.2019.10.005 · Cited by 3,225 · cited 3× · see citing works
“The senescence-associated secretory phenotype includes the production of matrix metalloproteinases, cytokines, chemokines, nitric oxide, and reactive oxygen species (Gorgoulis et al., 2019).”
BackgroundInfluentialGUNDERSEN, H. J. G., BENDTSEN, T. F., KORBO, L., MARCUSSEN, N., MØLLER, A., NIELSEN, K., NYENGAARD, J. R., PAKKENBERG, B., SØRENSEN, F. B., VESTERBY, A., et al. (1988) · APMIS · doi:10.1111/j.1699-0463.1988.tb05320.x · Cited by 2,929 · see citing works
Geroscience: Linking Aging to Chronic Disease
Kennedy, B. K., Berger, S. L., Brunet, A., Campisi, J., Cuervo, A. M., Epel, E. S., Franceschi, C., Lithgow, G. J., Morimoto, R. I., Pessin, J. E., et al. (2014) · Cell · doi:10.1016/j.cell.2014.10.039 · Cited by 2,764 · see citing works
Single-cell transcriptomic analysis of Alzheimer’s disease
Mathys, H., Davila-Velderrain, J., Peng, Z., Gao, F., Mohammadi, S., Young, J. Z., Menon, M., He, L., Abdurrob, F., Jiang, X., et al. (2019) · Nature · doi:10.1038/s41586-019-1195-2 · Cited by 2,568 · see citing works
Identification of a unique TGF-β–dependent molecular and functional signature in microglia
Butovsky, O., Jedrychowski, M. P., Moore, C. S., Cialic, R., Lanser, A. J., Gabriely, G., Koeglsperger, T., Dake, B., Wu, P. M., Doykan, C. E., et al. (2014) · Nature Neuroscience · doi:10.1038/nn.3599 · Cited by 2,543 · see citing works
The unbiased estimation of number and sizes of arbitrary particles using the disector
Sterio, D. C. (1984) · Journal of Microscopy · doi:10.1111/j.1365-2818.1984.tb02501.x · Cited by 2,533 · see citing works
Clearance of senescent glial cells prevents tau-dependent pathology and cognitive decline
Bussian, T. J., Aziz, A., Meyer, C. F., Swenson, B. L., van Deursen, J. M., & Baker, D. J. (2018) · Nature · doi:10.1038/s41586-018-0543-y · Cited by 1,289 · see citing works
Transcriptomic analysis of purified human cortical microglia reveals age-associated changes
Galatro, T. F., Holtman, I. R., Lerario, A. M., Vainchtein, I. D., Brouwer, N., Sola, P. R., Veras, M. M., Pereira, T. F., Leite, R. E. P., Möller, T., et al. (2017) · Nature Neuroscience · doi:10.1038/nn.4597 · Cited by 741 · see citing works
Streit, W. J., Braak, H., Xue, Q.-S., & Bechmann, I. (2009) · Acta Neuropathologica · doi:10.1007/s00401-009-0556-6 · Cited by 727 · see citing works
Dystrophic microglia in the aging human brain
Streit, W. J., Sammons, N. W., Kuhns, A. J., & Sparks, D. L. (2004) · Glia · doi:10.1002/glia.10319 · Cited by 705 · see citing works
Hopperton, K. E., Mohammad, D., Trépanier, M. O., Giuliano, V, & Bazinet, R. P. (2018) · Molecular Psychiatry · doi:10.1038/mp.2017.246 · Cited by 567 · cited 4× · see citing works
“It has traditionally been held that morphologic changes in white matter microglia are related to neuroinflammation characterized by an increased expression of major histocompatibility complex class II and complement receptor C3bi (Hopperton et al., 2018).”
BackgroundInfluentialIron and neurodegeneration in the multiple sclerosis brain
Hametner, S., Wimmer, I., Haider, L., Pfeifenbring, S., Brück, W., & Lassmann, H. (2013) · Annals of Neurology · doi:10.1002/ana.23974 · Cited by 519 · see citing works
Simmons, D. A., Casale, M., Alcon, B., Pham, N., Narayan, N., & LYNCH, G. S. (2007) · Glia · doi:10.1002/glia.20526 · Cited by 277 · see citing works
Orre, M., Kamphuis, W., Osborn, L. M., Melief, J., Kooijman, L., Huitinga, I., Klooster, J., Bossers, K., & Hol, E. M. (2013) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2013.07.008 · Cited by 269 · see citing works
Lopes, K. O., Sparks, D. L., & Streit, W. J. (2008) · Glia · doi:10.1002/glia.20678 · Cited by 262 · see citing works
Bachstetter, A. D., Van Eldik, L. J., Schmitt, F. A., Neltner, J. H., Ighodaro, E. T., Webster, S. J., Patel, E., Abner, E. L., Kryscio, R. J., & Nelson, P. T. (2015) · Acta Neuropathologica Communications · doi:10.1186/s40478-015-0209-z · Cited by 258 · see citing works
Self-citationDavies, D. S., Ma, J., Jegathees, T., & Goldsbury, C. (2017) · Brain Pathology · doi:10.1111/bpa.12456 · Cited by 251 · see citing works
Soluble phospho-tau from Alzheimer’s disease hippocampus drives microglial degeneration
Sanchez-Mejias, E., Navarro, V., Jimenez, S., Sanchez-Mico, M., Sanchez-Varo, R., Nuñez-Diaz, C., Trujillo-Estrada, L., Davila, J. C., Vizuete, M., Gutierrez, A., et al. (2016) · Acta Neuropathologica · doi:10.1007/s00401-016-1630-5 · Cited by 175 · see citing works
Ritzel, R. M., Doran, S. J., Glaser, E. P., Meadows, V. E., Faden, A. I., Stoica, B. A., & Loane, D. J. (2019) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2019.02.010 · Cited by 156 · see citing works
Dystrophic microglia in late‐onset Alzheimer's disease
Streit, W. J., Khoshbouei, H., & Bechmann, I. (2020) · Glia · doi:10.1002/glia.23782 · Cited by 152 · see citing works
Inhomogeneous distribution of Iba‐1 characterizes microglial pathology in Alzheimer's disease
Tischer, J., Krueger, M., Mueller, W. C., Staszewski, O., Prinz, M., Streit, W. J., & Bechmann, I. (2016) · Glia · doi:10.1002/glia.23024 · Cited by 117 · see citing works
Transmitting senescence to the cell neighbourhood
Hoare, M., & Narita, M. (2013) · Nature Cell Biology · doi:10.1038/ncb2811 · Cited by 108 · see citing works
Neuroinflammation in Alzheimer’s disease wanes with age
Hoozemans, J. J., Rozemuller, A. J., van Haastert, E. S., Eikelenboom, P., & van Gool, W. A. (2011) · Journal of Neuroinflammation · doi:10.1186/1742-2094-8-171 · Cited by 100 · see citing works
A limited capacity for microglial repopulation in the adult brain
Najafi, A. R., Crapser, J., Jiang, S., Ng, W., Mortazavi, A., West, B. L., & Green, K. N. (2018) · Glia · doi:10.1002/glia.23477 · Cited by 99 · see citing works
Verina, T., Kiihl, S. F., Schneider, J. S., & Guilarte, T. R. (2010) · NeuroToxicology · doi:10.1016/j.neuro.2010.11.003 · Cited by 81 · see citing works
Microglia in dementia with Lewy bodies
Streit, W. J., & Xue, Q. (2015) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2015.10.012 · Cited by 77 · see citing works
van Olst, L., Verhaege, D., Franssen, M., Kamermans, A., Roucourt, B., Carmans, S., Ytebrouck, E., van der Pol, S. M. A., Wever, D. D., Popovic, M. A., et al. (2020) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2020.01.003 · Cited by 75 · see citing works
Microglial pathology in Down syndrome
Xue, Q., & Streit, W. J. (2011) · Acta Neuropathologica · doi:10.1007/s00401-011-0864-5 · Cited by 72 · see citing works
Michalke, B., Willkommen, D., & Venkataramani, V. (2019) · Frontiers in Chemistry · doi:10.3389/fchem.2019.00136 · Cited by 47 · see citing works
Rodríguez-Callejas, J. D., Cuervo-Zanatta, D., Rosas‐Arellano, A., Fonta, C., Fuchs, E., & Perez‐Cruz, C. (2019) · American Journal of Primatology · doi:10.1002/ajp.22956 · Cited by 38 · see citing works
Microglia changes associated to Alzheimer’s disease pathology in aged chimpanzees
Edler, M., Sherwood, C., Meindl, R., Munger, E. L., Hopkins, W. D., Ely, J., Erwin, J., Perl, D. P., Mufson, E., Hof, P. R., et al. (2018) · The Journal of comparative neurology · doi:10.1002/cne.24484 · Cited by 32 · see citing works
Gál, J., Chen, J., Katsumata, Y., Fardo, D. W., Wang, W., Artiushin, S., PRICE, D. A., Anderson, S., Patel, E., Zhu, H., et al. (2017) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlx097 · Cited by 28 · see citing works
Self-citationRodríguez-Callejas, J. D., Fuchs, E., & Perez‐Cruz, C. (2020) · Glia · doi:10.1002/glia.23804 · Cited by 26 · see citing works
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Alzheimer’s disease: insights into pathology, molecular mechanisms, and therapy
Zheng, Q., & Wang, X. (2024) · Protein & Cell · doi:10.1093/procel/pwae026 · Cited by 454 · see citing works
Cellular senescence at the crossroads of inflammation and Alzheimer's disease
Guerrero, A., De Strooper, B., & Arancibia-Cárcamo, I. L. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2021.06.007 · Cited by 236 · see citing works
Transcriptional and epigenetic decoding of the microglial aging process
Li, X., Li, Y., Jin, Y., Zhang, Y., Wu, J., Xu, Z., Huang, Y., Cai, L., Gao, S., Liu, T., et al. (2023) · Nature Aging · doi:10.1038/s43587-023-00479-x · Cited by 225 · see citing works
Autophagy enables microglia to engage amyloid plaques and prevents microglial senescence
Choi, I., Wang, M., Yoo, S., Xu, P., Seegobin, S. P., Li, X., Han, X., Wang, Q., Peng, J., Zhang, B., et al. (2023) · Nature Cell Biology · doi:10.1038/s41556-023-01158-0 · Cited by 202 · see citing works
Jin, M., Xu, R., Wang, L., Alam, M. M., Ma, Z., Zhu, S., Martini, A. C., Jadali, A., Bernabucci, M., Xie, P., et al. (2022) · Cell Stem Cell · doi:10.1016/j.stem.2022.06.007 · Cited by 174 · see citing works
Microglia regulation of central nervous system myelin health and regeneration
Kent, S. A., & Miron, V. E. (2024) · Nature Reviews Immunology · doi:10.1038/s41577-023-00907-4 · Cited by 183 · see citing works
Lau, V. Z., Ramer, L. M., & Tremblay, M. (2023) · Nature Communications · doi:10.1038/s41467-023-37304-3 · Cited by 168 · see citing works
Cellular senescence in brain aging and neurodegeneration
dos Santos, L. M., Trombetta-Lima, M., Eggen, B. J. L., & Demaria, M. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.102141 · Cited by 158 · see citing works
Zhuang, H., Yao, X., Li, H., Li, Q., Yang, C., Wang, C., Xu, D., Xiao, Y., Gao, Y. J., Gao, J., et al. (2021) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2021.11.018 · Cited by 147 · see citing works
Emerging role of senescent microglia in brain aging-related neurodegenerative diseases
Rim, C., You, M., Nahm, M., & Kwon, M. (2024) · Translational Neurodegeneration · doi:10.1186/s40035-024-00402-3 · Cited by 147 · see citing works
Gaikwad, S., Senapati, S., Haque, M. A., & Kayed, R. (2024) · Alzheimer's & Dementia · doi:10.1002/alz.13490 · Cited by 117 · see citing works
Augusto‐Oliveira, M., Arrifano, G. D. P., Delage, C. I., Tremblay, M., Lopez, M. E. C., & Verkhratsky, A. (2021) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12797 · Cited by 107 · see citing works
Dubois, B., López‐Arrieta, J., Lipschitz, S., Doskas, T. K., Spiru, L., Moroz, S., Venger, O., Vermersch, P., Moussy, A., Mansfield, C. D., et al. (2023) · Alzheimer s Research & Therapy · doi:10.1186/s13195-023-01169-x · Cited by 110 · see citing works
Quantifying microglial morphology: an insight into function
Green, T. R. F., & Rowe, R. K. (2024) · Clinical & Experimental Immunology · doi:10.1093/cei/uxae023 · Cited by 106 · see citing works
Dysregulation of Systemic Immunity in Aging and Dementia
Lutshumba, J., Nikolajczyk, B. S., & Bachstetter, A. D. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.652111 · Cited by 103 · see citing works
Self-citationMicroglia dynamics in aging-related neurobehavioral and neuroinflammatory diseases
Javanmehr, N., Saleki, K., Alijanizadeh, P., & Rezaei, N. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-022-02637-1 · Cited by 103 · see citing works
Glaucoma: from pathogenic mechanisms to retinal glial cell response to damage
Fernández‐Albarral, J. A., Ramirez, A. I., de Hoz, R., Matamoros, J. A., Salobrar‐García, E., Elvira‐Hurtado, L., López‐Cuenca, I., Sánchez-Puebla, L., Salazar, J. J., & Ramirez, J. M. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1354569 · Cited by 99 · see citing works
Senescent Microglia: The Key to the Ageing Brain?
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Jurcău, M. C., Jurcău, A., Cristian, A., Hogea, V. O., Diaconu, R. G., & Nunkoo, V. S. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms251910535 · Cited by 90 · see citing works
Different phenotypes of microglia in animal models of Alzheimer disease
Wei, Y., & Li, X. (2022) · Immunity & Ageing · doi:10.1186/s12979-022-00300-0 · Cited by 71 · see citing works
Wang, Q., Wang, M., Choi, I., Sarrafha, L., Liang, M., Ho, L., Farrell, K. W., Beaumont, K. G., Sebra, R., Sanctis, C. D., et al. (2024) · Science Advances · doi:10.1126/sciadv.adi8287 · Cited by 82 · see citing works
Microbiota‐microglia connections in age‐related cognition decline
Zhou, R., Qian, S., Cho, W. C. S., Zhou, J., Jin, C., Zhong, Y., Wang, J., Zhang, X., Xu, Z., Tian, M., et al. (2022) · Aging Cell · doi:10.1111/acel.13599 · Cited by 71 · see citing works
Neurovascular unit, neuroinflammation and neurodegeneration markers in brain disorders
Kempuraj, D., Dourvetakis, K. D., Cohen, J., Valladares, D. S., Joshi, R. S., Kothuru, S. P., Anderson, T., Chinnappan, B., Cheema, A. K., Klimas, N. G., et al. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1491952 · Cited by 75 · see citing works
Untangling senescent and damage‐associated microglia in the aging and diseased brain
Ng, P. Y., McNeely, T. L., & Baker, D. J. (2023) · The FEBS Journal · doi:10.1111/febs.16315 · Cited by 68 · see citing works
Boza-Serrano, A., Vrillon, A., Minta, K., Paulus, A., Camprubí-Ferrer, L., Garcia, M., Andreasson, U., Antonell, A., Wennström, M., Gouras, G., et al. (2022) · Acta Neuropathologica · doi:10.1007/s00401-022-02469-6 · Cited by 66 · see citing works
Control of Neuroinflammation through Radiation-Induced Microglial Changes
Boyd, A., Byrne, S., Middleton, R. J., Banati, R. B., & Liu, G. J. (2021) · Cells · doi:10.3390/cells10092381 · Cited by 62 · see citing works
Aged Microglia in Neurodegenerative Diseases: Microglia Lifespan and Culture Methods
Yoo, H.-J., & Kwon, M. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.766267 · Cited by 63 · see citing works
Fernando, K., & Wijayasinghe, Y. S. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.746631 · Cited by 57 · see citing works
The Influence of Virus Infection on Microglia and Accelerated Brain Aging
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Inflammatory Biomarkers in Addictive Disorders
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Glial AP1 is activated with aging and accelerated by traumatic brain injury
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Malvaso, A., Gatti, A., Negro, G., Calatozzolo, C., Medici, V., & Poloni, T. E. (2023) · Cells · doi:10.3390/cells12242824 · Cited by 51 · see citing works
McFarland, K. N., & Chakrabarty, P. (2022) · Neurotherapeutics · doi:10.1007/s13311-021-01179-3 · Cited by 48 · see citing works
Microglia Phenotypes Converge in Aging and Neurodegenerative Disease
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White matter-associated microglia: New players in brain aging and neurodegenerative diseases
Ahn, K., Lee, S., & Mook‐Jung, I. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101574 · Cited by 46 · see citing works
The aging immune system in Alzheimer’s and Parkinson’s diseases
Heavener, K. S., & Bradshaw, E. M. (2022) · Seminars in Immunopathology · doi:10.1007/s00281-022-00944-6 · Cited by 50 · see citing works
Serrano, G. E., Walker, J. E., Tremblay, C., Piras, I. S., Huentelman, M. J., Belden, C. M., Goldfarb, D., Shprecher, D., Atri, A., Adler, C. H., et al. (2022) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlac056 · Cited by 44 · see citing works
Neumann, P., Lenz, D. E., Streit, W. J., & Bechmann, I. (2022) · Glia · doi:10.1002/glia.24282 · Cited by 45 · see citing works
Bowirrat, A. (2022) · Journal of Personalized Medicine · doi:10.3390/jpm12111817 · Cited by 45 · see citing works
Carrier, M., Šimončičová, E., St‐Pierre, M., McKee, C., & Tremblay, M. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.749737 · Cited by 37 · see citing works
McKee, C., Hoffos, M., Vecchiarelli, H. A., & Tremblay, M. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1125982 · Cited by 38 · see citing works
Intracerebral Hemorrhage: The Effects of Aging on Brain Injury
Watson, N. J., Bonsack, F., & Sukumari‐Ramesh, S. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.859067 · Cited by 37 · see citing works
Streit, W. J., Rotter, J., Winter, K., Müller, W. C., Khoshbouei, H., & Bechmann, I. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-215334 · Cited by 36 · see citing works
Microglia in the context of multiple sclerosis
Zhang, X., Chen, F., Sun, M., Wu, N., Liu, B., Yi, X., Ge, R., & Fan, X. (2023) · Frontiers in Neurology · doi:10.3389/fneur.2023.1157287 · Cited by 35 · see citing works
Gebril, H. M., Aryasomayajula, A., de Lima, M. R. N., Uhrich, K. E., & Moghe, P. V. (2024) · Translational Neurodegeneration · doi:10.1186/s40035-023-00393-7 · Cited by 36 · see citing works
Senescent Microglia Represent a Subset of Disease-Associated Microglia in P301S Mice
Ng, P. Y., Zhang, C., Li, H., & Baker, D. J. (2023) · Journal of Alzheimer s Disease · doi:10.3233/jad-230109 · Cited by 38 · see citing works
Roy, N., Haq, I., Ngo, J. C., Bennett, D. A., Teich, A. F., Jager, P. L. D., Olah, M., & Sher, F. (2024) · Acta Neuropathologica · doi:10.1007/s00401-024-02835-6 · Cited by 35 · see citing works
The Hallmarks of Ageing in Microglia
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Lipid droplet accumulation in microglia and their potential roles
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Ben‐Azu, B., del Re, E. C., VanderZwaag, J., Carrier, M., Keshavan, M. S., Khakpour, M., & Tremblay, M. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1139357 · Cited by 32 · see citing works
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Ernst, T., Ryan, M. C., Liang, H., Wang, J. P., Cunningham, E. P., Saleh, M. G., Kottilil, S., & Chang, L. (2023) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiad309 · Cited by 31 · see citing works
The Pathological Activation of Microglia Is Modulated by Sexually Dimorphic Pathways
O'Connor, J. L., & Nissen, J. C. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054739 · Cited by 31 · see citing works
Jidigam, V. K., Singh, R., Batoki, J. C., Milliner, C., Sawant, O. B., Bonilha, V. L., & Rao, S. (2021) · Graefe s Archive for Clinical and Experimental Ophthalmology · doi:10.1007/s00417-021-05460-1 · Cited by 29 · see citing works
Varied Composition and Underlying Mechanisms of Gut Microbiome in Neuroinflammation
Farooq, R. K., Alamoudi, W., Alhibshi, A., Rehman, S., Sharma, A. R., & Abdulla, F. A. (2022) · Microorganisms · doi:10.3390/microorganisms10040705 · Cited by 30 · see citing works
Wątroba, M., & Szukiewicz, D. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.962769 · Cited by 29 · see citing works
Distinguishing features of depression in dementia from primary psychiatric disease
Fisher, D. W., Dunn, J. T., & Dong, H. (2024) · Discover Mental Health · doi:10.1007/s44192-023-00057-y · Cited by 30 · see citing works
Animal and Cellular Models of Alzheimer’s Disease: Progress, Promise, and Future Approaches
Trujillo‐Estrada, L., Sánchez‐Mejías, E., Sanchez-Varo, R. M., García‐León, J. A., Nuñez‐Diaz, C., Dávila, J. C., Vitórica, J., LaFerla, F. M., Moreno‐González, I., Gutiérrez, A., et al. (2021) · The Neuroscientist · doi:10.1177/10738584211001753 · Cited by 28 · see citing works
DeVries, S. A., Conner, B., Dimovasili, C., Moore, T. L., Medalla, M., Mortazavi, F., & Rosene, D. L. (2023) · GeroScience · doi:10.1007/s11357-023-01014-x · Cited by 27 · see citing works
Tang, J., Yousaf, M., Wu, Y., Li, Q., Xu, Y., & Liu, D. (2023) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2023.127553 · Cited by 27 · see citing works
The role of microglia in neurodegenerative diseases: from the perspective of ferroptosis
Liu, Y.-J., Jia, G.-R., Zhang, S.-H., Guo, Y., Ma, X.-Z., Xu, H.-M., & Xie, J.-X. (2025) · Acta Pharmacologica Sinica · doi:10.1038/s41401-025-01560-4 · Cited by 29 · see citing works
Ayton, S., Janelidze, S., Kalinowski, P., Palmqvist, S., Belaidi, A. A., Stomrud, E., Roberts, A., Roberts, B. R., Hansson, O., & Bush, A. I. (2022) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2022-330052 · Cited by 24 · see citing works
Ensheathing glia promote increased lifespan and healthy brain aging
Sheng, L., Shields, E. J., Gospočić, J., Sorida, M., Ju, L., Byrns, C. N., Carranza, F. R., Berger, S. L., Bonini, N. M., & Bonasio, R. (2023) · Aging Cell · doi:10.1111/acel.13803 · Cited by 21 · see citing works
Biological agents and the aging brain: glial inflammation and neurotoxic signaling
Latham, A. S., Moreno, J. A., & Geer, C. E. (2023) · Frontiers in Aging · doi:10.3389/fragi.2023.1244149 · Cited by 25 · see citing works
Single-cell transcriptomic atlas of the human substantia nigra in Parkinson’s diseasePreprint
Wang, Q., Wang, M., Choi, I., Ho, L., Farrell, K. W., Beaumont, K. G., Sebra, R., Crary, J. F., Davis, D. A., Sun, X., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.03.25.485846 · Cited by 22 · see citing works
Microglial senescence in neurodegeneration: Insights, implications, and therapeutic opportunities
Olajide, T. S., Oyerinde, T. O., Omotosho, O. I., Okeowo, O. M., Olajide, O. J., & Ijomone, O. M. (2024) · Neuroprotection/Neuroprotection (Chichester, England. Print) · doi:10.1002/nep3.56 · Cited by 24 · see citing works
Jekabsone, A., Jankevičiūtė, S., Pampuščenko, K., Borutaitė, V., & Morkūnienė, R. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241512315 · Cited by 21 · see citing works
Augusto‐Oliveira, M., Arrifano, G. D. P., Leal-Nazaré, C. G., Chaves-Filho, A. J. M., Santos-Sacramento, L., Lopes-Araújo, A., Tremblay, M., & Lopez, M. E. C. (2025) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2025.106091 · Cited by 25 · see citing works
The Complementary Role of Morphology in Understanding Microglial Functional Heterogeneity
Godeanu, S., & Cătălin, B. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26083811 · Cited by 21 · see citing works
Microglia in brain aging: An overview of recent basic science and clinical research developments
Fan, H., Zhang, M., Wen, J., Wang, S., Yuan, M., Sun, H., Shu, L., Xu, Y., Pu, Y., & Cai, Z. (2023) · Journal of Biomedical Research · doi:10.7555/jbr.37.20220220 · Cited by 22 · see citing works
Exploring the link between dystrophic microglia and the spread of Alzheimer's neuropathology
Shahidehpour, R. K., Nelson, P. T., Katsumata, Y., & Bachstetter, A. D. (2024) · Brain · doi:10.1093/brain/awae258 · Cited by 20 · see citing works
Self-citationInfantino, R., Boccella, S., Scuteri, D., Perrone, M., Ricciardi, F., Vitale, R. M., Bonsale, R., Parente, A., Allocca, I., Virtuoso, A., et al. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.113844 · Cited by 19 · see citing works
Liu, Y., Hong, T., Lv, M., Guo, X., Zhang, P. Y., Yan, A., & Wei, W. (2025) · Alzheimer s Research & Therapy · doi:10.1186/s13195-025-01783-x · Cited by 20 · see citing works
Chen, C., & Brumberg, J. C. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.770453 · Cited by 19 · see citing works
Sanchez, K. G., Darling, J. S., Kakkar, R., Wu, S. L., Zentay, A., Lowry, C. A., & Fonken, L. K. (2022) · Scientific Reports · doi:10.1038/s41598-022-05275-y · Cited by 19 · see citing works
Bobotis, B. C., Halvorson, T., Carrier, M., & Tremblay, M. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1317125 · Cited by 21 · see citing works
Cárdenas‐Tueme, M., Trujillo-Villarreal, L. A., Ramı́rez-Amaya, V., Garza‐Villarreal, E. A., Camacho‐Morales, A., & Reséndez‐Pérez, D. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119039 · Cited by 17 · see citing works
Association between APOE genotype and microglial cell morphology
Kloske, C. M., Gearon, M. D., Weekman, E. M., Rogers, C. B., Patel, E., Bachstetter, A. D., Nelson, P. T., & Wilcock, D. M. (2023) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlad031 · Cited by 17 · see citing works
Self-citationImmunological aspects of central neurodegeneration
Niso‐Santano, M., Fuentes, J. M., & Galluzzi, L. (2024) · Cell Discovery · doi:10.1038/s41421-024-00666-z · Cited by 16 · see citing works
Morderer, D., Wren, M. C., Liu, F., Kouri, N., Maistrenko, A., Khalil, B., Pobitzer, N., Salemi, M., Phinney, B. S., Bu, G., et al. (2025) · Molecular Neurodegeneration · doi:10.1186/s13024-025-00817-0 · Cited by 19 · see citing works
Lau, V. Z., Awogbindin, I. O., Frenkel, D., Whitehead, S. N., & Tremblay, M. (2025) · Alzheimer s & Dementia · doi:10.1002/alz.70363 · Cited by 15 · see citing works
Borelli, W. V., de Senna, P. N., Brum, W. S., Schuh, A. F. S., Zimmer, E. R., Chaves, M. L. F., & Castilhos, R. M. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.789190 · Cited by 15 · see citing works
McCaffrey, D., Lawther, A. J., Weickert, C. S., & Walker, A. K. (2022) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2022.105938 · Cited by 15 · see citing works
Zhuang, H., Li, Q., Sun, C., Xu, D., Gan, G., Zhang, C., Chen, C., Yuan, Y., Liu, L., Xiao, Y. M., et al. (2023) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2023.09.002 · Cited by 15 · see citing works
Interleukin-33 ameliorates perioperative neurocognitive disorders by modulating microglial state
Yang, D., Sun, Y., Lin, D., Li, S., Zhang, Y., Wu, A., & Wei, C. (2024) · Neuropharmacology · doi:10.1016/j.neuropharm.2024.109982 · Cited by 15 · see citing works
Exploring microglial replacement: From disease models to clinical translation
Zhou, K., Wang, Y., Xu, Y., Zhang, Y., & Zhu, C. (2025) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2025.06.011 · Cited by 13 · see citing works
Scott, A., Palmer, D. B., Newell, B., Lin, I., Cayton, C. A., Paulson, A., Remde, P., & Richard, J. M. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.0013-23.2023 · Cited by 13 · see citing works
Insights into the Impact of Gold Nanoclusters Au10SG10 on Human Microglia.
Maysinger, D., Maršić, Ž. S., Gran, E. R., Shobo, A., Macairan, J.-R., Zhang, I., Bakulić, M. P., Antoine, R., Multhaup, G., & Bonačić-Koutecký, V. (2022) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.1c00621 · Cited by 10 · see citing works
Castro, R. W., Lopes, M. C., Biase, L. M. D., & Valdez, G. (2023) · Glia · doi:10.1002/glia.24470 · Cited by 10 · see citing works
Neutrophils in the Focus: Impact on Neuroimmune Dynamics and the Gut–Brain Axis
Kršek, A., & Batičić, L. (2024) · Gastrointestinal Disorders · doi:10.3390/gidisord6030039 · Cited by 12 · see citing works
Bagheri, S., Saboury, A. A., & Saso, L. (2024) · Cells · doi:10.3390/cells13151293 · Cited by 12 · see citing works
Glycolytic metabolism supports microglia training during age-related neurodegeneration
Camacho‐Morales, A. (2022) · Pharmacological Reports · doi:10.1007/s43440-022-00363-2 · Cited by 11 · see citing works
Toledano‐Díaz, A., Álvarez, M., & Tolédano, A. (2022) · Journal of Central Nervous System Disease · doi:10.1177/11795735221128703 · Cited by 11 · see citing works
Alcohol induces apoptosis and autophagy in microglia BV-2 cells
Wang, L., Song, L., Ma, J., Wang, H., Li, Y., & Huang, D. (2023) · Food and Chemical Toxicology · doi:10.1016/j.fct.2023.113849 · Cited by 11 · see citing works
Maksour, S., & Ooi, L. (2023) · Journal of Neurochemistry · doi:10.1111/jnc.15885 · Cited by 11 · see citing works
Xie, X., Liu, J., Liang, W., Zhang, Y., Gong, X., Yuan, S., Qi, C., Huang, M., Shi, L., Hou, M., et al. (2026) · Immunity · doi:10.1016/j.immuni.2026.01.014 · Cited by 10 · see citing works
Daga, K. R., Priyadarshani, P., Larey, A. M., Rui, K., Mortensen, L. J., & Marklein, R. A. (2021) · Current Opinion in Biomedical Engineering · doi:10.1016/j.cobme.2021.100352 · Cited by 10 · see citing works
Szabó, M., Lajkó, N., Dulka, K., Barczánfalvi, G., Lőrinczi, B., Szatmári, I., Mihály, A., Vécsei, L., & Gulya, K. (2023) · Scientific Reports · doi:10.1038/s41598-023-38107-8 · Cited by 10 · see citing works
Anwar, M. M., Pérez‐Martínez, L., & Pedraza‐Alva, G. (2024) · Immunological Investigations · doi:10.1080/08820139.2024.2358446 · Cited by 11 · see citing works
- Authors
- Shahidehpour, R. K., Higdon, R. E., Crawford, N. G., Neltner, J. H., Ighodaro, E. T., Patel, E., Price, D., Nelson, P. T., & Bachstetter, A. D.
- Affiliations
- University of Kentucky (US)
- University of Kentucky HealthCare (US)
- Corresponding author
- Bachstetter, Adam D.
- ORCID
- Venue
- Neurobiology of Aging
- Publisher
- Elsevier BV
- Published
- 2021-03
- Volume
- 99
- Pages
- 19-27
- ISSN
- 0197-4580 (ISSN-L)
- PMC
- PMC8293930
- OpenAlex
- W3120102977
- Cited by
- 173
- References
- 35
- Citations by year
- 2026: 16 · 2025: 31 · 2024: 27 · 2023: 35 · 2022: 39 · 2021: 25
- FWCI
- 12.58
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Neurobiology of Aging (publishedVersion, cc-by-nc-nd)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- UKnowledge (University of Kentucky) (submittedVersion, cc-by-nc-nd)
- Funders
- National Institute of General Medical Sciences (R35 GM124977)
- National Institutes of Health
- National Institute on Aging (P30 AG028383, R21AG066865)
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Neurology › Neurological Disease Mechanisms and Treatments
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
- Keywords
- microglial morphology, neurodegenerative diseases, healthy aging, cellular senescence, Alzheimer's disease, dementia with Lewy bodies, limbic-predominant age-related TDP-43 encephalopathy, iron homeostasis, hippocampus, frontal cortex, human brain
- MeSH terms
- Healthy Aging, Female, Frontal Lobe, Hippocampus, Homeostasis, Humans, Hypertrophy, Iron, Male, Cellular Senescence, Microglia, Neurodegenerative Diseases
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