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CD36 ligands promote sterile inflammation through assembly of a Toll-like receptor 4 and 6 heterodimer
Open accessAbstract
In atherosclerosis and Alzheimer's disease, deposition of the altered self components oxidized low-density lipoprotein (LDL) and amyloid-beta triggers a protracted sterile inflammatory response. Although chronic stimulation of the innate immune system is believed to underlie the pathology of these diseases, the molecular mechanisms of activation remain unclear. Here we show that oxidized LDL and amyloid-beta trigger inflammatory signaling through a heterodimer of Toll-like receptors 4 and 6. Assembly of this newly identified heterodimer is regulated by signals from the scavenger receptor CD36, a common receptor for these disparate ligands. Our results identify CD36-TLR4-TLR6 activation as a common molecular mechanism by which atherogenic lipids and amyloid-beta stimulate sterile inflammation and suggest a new model of TLR heterodimerization triggered by coreceptor signaling events.
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“Stewart and colleagues demonstrated that Aβ-mediated release of proinflammatory factors and neurotoxicity partially involved signaling through the CD36/ TLR4/TRL6 complex (108).”
From Microglia in Alzheimer's disease (2017) · cites this paper as [108]
In the citing paper
“CD36 mediates heterodimer formation of TLR4 and TLR6 (REF. 104), and this co-receptor complex upregulates the production of chemokines and cytokines such as pro-IL-1β through the activation of NF-κb.”
From Sterile inflammation: sensing and reacting to damage (2010) · cites this paper as [105]
In the citing paper
“The Soluble Aβ oligomers and Aβ fibrils can react to various receptors expressed by microglia, including CD14, CD36, CD47, α6β1 integrin, class A scavenger receptor, receptor for advanced glycosylation end products (RAGE) and TLRs (Stewart et al., 2010).”
From The role of microglia in retinal neurodegeneration: Alzheimer’s disease, parkinson, and glaucoma. (2017) · cites this paper as Stewart et al., 2010
In the citing paper
“The binding of Aβ to CD36 (cell surface microglial co-receptor) promotes the TLR4 and/or TLR6 phosphorylation and activation, resulting in the production of inflammatory cytokines and chemokines (Stewart et al., 2010).”
From The role of microglia in retinal neurodegeneration: Alzheimer’s disease, parkinson, and glaucoma. (2017) · cites this paper as Stewart et al., 2010
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Cites
Atherosclerosis--an inflammatory disease
Ross, R. (1999) · New England Journal of Medicine · doi:10.1056/nejm199901143400207 · Cited by 21,725
Akira, S., & Takeda, K. (2004) · Nature reviews. Immunology · doi:10.1038/nri1391 · Cited by 8,312
Recognition of microorganisms and activation of the immune response
Medzhitov, R. (2007) · Nature · doi:10.1038/nature06246 · Cited by 2,862
The NALP3 inflammasome is involved in the innate immune response to amyloid-β
Halle, A., Hornung, V., Petzold, G. C., Stewart, C. R., Monks, B. G., Reinheckel, T., Fitzgerald, K. A., Latz, E., Moore, K. J., & Golenbock, D. T. (2008) · Nature Immunology · doi:10.1038/ni.1636 · Cited by 2,441
Self-citationOzinsky, A., Underhill, D. M., Fontenot, J. D., Hajjar, A. M., Smith, K. D., Wilson, C. B., Schroeder, L. A., & Aderem, A. A. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.250476497 · Cited by 2,086
Collaborative Induction of Inflammatory Responses by Dectin-1 and Toll-like Receptor 2
Gantner, B. N., Simmons, R. M., Canavera, S. J., Akira, S., & Underhill, D. M. (2003) · The Journal of Experimental Medicine · doi:10.1084/jem.20021787 · Cited by 1,682
TRAM couples endocytosis of Toll-like receptor 4 to the induction of interferon-β
Kagan, J. C., Su, T., Horng, T., Chow, A. Y., Akira, S., & Medzhitov, R. M. (2008) · Nature Immunology · doi:10.1038/ni1569 · Cited by 1,310
Wyss-Coray (2006) · doi:10.1038/nm1484 · Cited by 1,284
Immortalization of murine microglial cells by a v-raf / v-myc carrying retrovirus
Blasi, E., Barluzzi, R., Bocchini, V., Mazzolla, R., & Bistoni, F. (1990) · Journal of Neuroimmunology · doi:10.1016/0165-5728(90)90073-v · Cited by 1,075
Kunjathoor, V., Febbraio, M., Podrez, E., Moore, K., Andersson, L., Koehn, S. L., Rhee, J. S., Silverstein, R., Hoff, H., & Freeman, M. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m209649200 · Cited by 1,064
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Items 601–700 of 1,001
Abuelezz, S. A., & Hendawy, N. (2021) · Life Sciences · doi:10.1016/j.lfs.2021.119310 · Cited by 50
Pathogenic Role of Scavenger Receptor CD36 in the Metabolic Syndrome and Diabetes
Kennedy, D. J., & Kashyap, S. R. (2011) · Metabolic Syndrome and Related Disorders · doi:10.1089/met.2011.0003 · Cited by 51
Perspectives for Monocyte/Macrophage-Based Diagnostics of Chronic Inflammation
Kzhyshkowska, J. G., Gudima, A., Moganti, K., Gratchev, A. N., & Orekhov, A. N. (2016) · Transfusion Medicine and Hemotherapy · doi:10.1159/000444943 · Cited by 50
Yao, P., Zhuo, S., Mei, H., Chen, X., Li, N., Zhu, T., Chen, S., Wang, J., Hou, R., & Le, Y. (2017) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.12757 · Cited by 51
Xiao, L., Luo, G., Guo, X., Jiang, C., Zeng, H., Zhou, F., Li, Y., Yu, J., & Yao, P. (2019) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2019.158531 · Cited by 50
Molecular Mechanism of Apoptosis by Amyloid β-Protein Fibrils Formed on Neuronal Cells
Takada, E., Okubo, K., Yano, Y., Iida, K., Someda, M., Hirasawa, A., Yonehara, S., & Matsuzaki, K. (2020) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.0c00011 · Cited by 50
Kuntić, M., Hahad, O., Münzel, T. F., & Daiber, A. (2024) · Antioxidants · doi:10.3390/antiox13030266 · Cited by 53
Guo, H., Feng, R.-X., Zhang, Y., Yu, Y., Lu, W., Liu, J.-J., Yang, S., Zhao, C., Zhang, Z.-L., Yu, S., et al. (2024) · Cell Reports Medicine · doi:10.1016/j.xcrm.2024.101592 · Cited by 50
Shi, X.-Z., Yang, M., Kang, X.-L., Li, Y.-X., Hong, P.-P., Zhao, X., Vasta, G. R., & Wang, J. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2216574120 · Cited by 50
Baines, R. J., Chana, R. S., Hall, M., Febbraio, M., Kennedy, D. J., & Brunskill, N. J. (2012) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00021.2012 · Cited by 47
Postulates for validating TLR4 agonists
Manček‐Keber, M., & Jerala, R. (2014) · European Journal of Immunology · doi:10.1002/eji.201444462 · Cited by 51
The multiple roles of fatty acid handling proteins in brain
Moullé, V. S. F., Cansell, C., Luquet, S., & Cruciani-Guglielmacci, C. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00385 · Cited by 49
Khan, A. A., Khan, Z., & Warnakulasuriya, S. (2016) · Annals of Oncology · doi:10.1093/annonc/mdw053 · Cited by 50
Doens, D., Valiente, P. A., Mfuh, A. M., Vo, A. X. T., Tristan, A., Carreño, L., Quijada, M. R., Nguyen, V. T., Perry, G. L., Larionov, O. V., et al. (2017) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.6b00386 · Cited by 49
Jongstra‐Bilen, J., Zhang, C., Wisnicki, T., Li, M. K., White-Alfred, S., Ilaalagan, R., Ferri, D., Deonarain, A. R., Wan, M. H., Hyduk, S. J., et al. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1601363 · Cited by 50
Kong, T., Gong, Y., Liú, Y., Wen, X., Tran, N. T., Aweya, J. J., Zhang, Y., Ma, H., Zheng, H., & Li, S. (2018) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2018.04.027 · Cited by 49
Hao, Y., Guo, M., Feng, Y., Dong, Q., & Cui, M. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.00058 · Cited by 51
Efferocytic Defects in Early Atherosclerosis Are Driven by GATA2 Overexpression in Macrophages
Yin, C., Vrieze, A. M., Rosoga, M., Akingbasote, J. A., Pawlak, E. N., Jacob, R. A., Hu, J. K., Sharma, N., Dikeakos, J. D., Barra, L., et al. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.594136 · Cited by 48
McFarland, K. N., & Chakrabarty, P. (2022) · Neurotherapeutics · doi:10.1007/s13311-021-01179-3 · Cited by 48
Pharmacological inhibition of inflammatory pathways for the prevention of preterm birth
Keelan, J. A. (2011) · Journal of Reproductive Immunology · doi:10.1016/j.jri.2010.11.003 · Cited by 48
Alam, M., Alam, Q., Kamal, M., Abuzenadah, A., & Haque, A. (2014) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/18715273113126660151 · Cited by 47
The Intriguing Role of TLR Accessory Molecules in Cardiovascular Health and Disease
Bezhaeva, T., Karper, J. C., Quax, P. H. A., & de Vries, M. R. (2022) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2022.820962 · Cited by 48
Wang, S., Han, Y., Liu, R., Hou, M., Neumann, D., Zhang, J., Wang, F., Li, Y., Zhao, X., Schianchi, F., et al. (2024) · Circulation Research · doi:10.1161/circresaha.123.322910 · Cited by 47
Sweepers in the CNS: Microglial Migration and Phagocytosis in the Alzheimer Disease Pathogenesis
Noda, M., & Suzumura, A. (2012) · International Journal of Alzheimer s Disease · doi:10.1155/2012/891087 · Cited by 52
Toll‐like receptors: Role in inflammation and therapeutic potential
Kay, E., Scotland, R. S., & Whiteford, J. R. (2013) · BioFactors · doi:10.1002/biof.1156 · Cited by 50
Biswas, S., Liang, X., Panigrahi, S., Zimman, A., Wang, H., Yakubenko, V. P., Byzova, T. V., Salomon, R. G., & Podrez, E. A. (2016) · Blood · doi:10.1182/blood-2015-08-664300 · Cited by 47
Electronegative LDL Promotes Inflammation and Triglyceride Accumulation in Macrophages
Puig, N., Montolio, L., Camps‐Renom, P., Navarra, L., Jiménez‐Altayó, F., Jiménez‐Xarrié, E., Sánchez‐Quesada, J. L., & Benı́tez, S. (2020) · Cells · doi:10.3390/cells9030583 · Cited by 47
Gao, S., Jiang, Y., Chen, Z., Zhao, X.-Q., Gu, J., Wu, H., Liao, Y., Sun, H., Wang, J., & Chen, W. (2022) · Current Neuropharmacology · doi:10.2174/1570159x21666221216162606 · Cited by 51
Mechanistic and therapeutic role of NLRP3 inflammasome in the pathogenesis of Alzheimer's disease
Jha, D., Bakker, E. N. T. P., & Kumar, R. K. (2023) · Journal of Neurochemistry · doi:10.1111/jnc.15788 · Cited by 48
Macrophage Activation by Ursolic and Oleanolic Acids during Mycobacterial Infection
López-García, S., Castañeda‐Sánchez, J. I., Jiménez-Arellanes, M. A., Domínguez‐López, M. L., Castro-Mussot, M. E., Hernández‐Sánchez, J., & Luna‐Herrera, J. (2015) · Molecules · doi:10.3390/molecules200814348 · Cited by 46
Leishmania amazonensis Engages CD36 to Drive Parasitophorous Vacuole Maturation
Okuda, K., Tong, M., Brian, D., Moore, K. J., Gazzinelli, R. T., & Silverman, N. S. (2016) · PLoS Pathogens · doi:10.1371/journal.ppat.1005669 · Cited by 46
Self-citationCamandola, S., & Mattson, M. P. (2017) · Obesity · doi:10.1002/oby.21871 · Cited by 46
Shmuel-Galia, L., Klug, Y. A., Porat, Z., Charni‐Natan, M., Zarmi, B., & Shai, Y. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.784983 · Cited by 46
García-González, P. A., Cabral‐Miranda, F., Hetz, C. A., & Osorio, F. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02541 · Cited by 46
Yang, K., Zeng, C. C., Wang, C., Sun, M., Yin, D., & Sun, T. (2020) · Molecules · doi:10.3390/molecules25225439 · Cited by 49
Hohenhaus, D. M., Schaale, K., Cao, K. L., Seow, V., Iyer, A., Fairlie, D. P., & Sweet, M. J. (2013) · Immunobiology · doi:10.1016/j.imbio.2013.07.001 · Cited by 45
Karper, J. C., Ewing, M. M., Habets, K. L. L., de Vries, M. R., Peters, E. A. B., van Oeveren‐Rietdijk, A. M., de Boer, H. C., Hamming, J. F., Kuiper, J., Kandimalla, E. R., et al. (2012) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.112.249391 · Cited by 45
Xu, C., Zhang, C., Ji, J., Wang, C., Yang, J., Geng, B., Zhao, T., Zhou, H., Mu, X., Pan, J., et al. (2017) · Hepatology · doi:10.1002/hep.29716 · Cited by 45
Shao, D., Lian, Z., Di, Y., Zhang, L., Rajoka, M. S. R., Zhang, Y., Kong, J., Jiang, C., & Shi, J. (2018) · npj Science of Food · doi:10.1038/s41538-018-0022-8 · Cited by 49
Nascè, A., Gariani, K., Jornayvaz, F. R., & Szántó, I. (2022) · Antioxidants · doi:10.3390/antiox11061131 · Cited by 49
LXRα Regulates oxLDL-Induced Trained Immunity in Macrophages
Findeisen, H. M., Voges, V. C., Braun, L. C., Sonnenberg, J., Schwarz, D., Körner, H., Reinecke, H., & Sohrabi, Y. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23116166 · Cited by 44
Wu, C.-Y., Huang, C.-X., Lao, X., Zhou, Z.-W., Jian, J.-H., Li, Z., Wu, Y., Liu, Z., Chen, L., Liu, L., et al. (2025) · Cell · doi:10.1016/j.cell.2025.06.027 · Cited by 44
Pihlgren, M., Silva, A. B., Madani, R., Giriens, V., Waeckerle‐Men, Y., Fettelschoss‐Gabriel, A., Hickman, D. T., López-Deber, M. P., Ndao, D. M., Vukicevic, M., et al. (2012) · Blood · doi:10.1182/blood-2012-02-413831 · Cited by 44
Amyloidosis in Retinal Neurodegenerative Diseases
Masuzzo, A., Dinet, V., Cavanagh, C., Mascarelli, F., & Krantic, S. M. (2016) · Frontiers in Neurology · doi:10.3389/fneur.2016.00127 · Cited by 45
Microglia Function in the Normal Brain
Rommy von Bernhardi, M., Heredia, F., Salgado, N., & Muñoz, P. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-40764-7_4 · Cited by 47
Na, H. S., Kwon, J.-E., Lee, S., Jhun, J., Kim, S., Kim, S. Y., Kim, E., Jung, K., Park, S., & Cho, M. (2017) · American Journal Of Pathology · doi:10.1016/j.ajpath.2016.12.023 · Cited by 45
Rahman, K., & Fisher, E. A. A. (2018) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2018.00032 · Cited by 48
Genetics of Malaria Inflammatory Responses: A Pathogenesis Perspective
Penha‐Gonçalves, C. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01771 · Cited by 44
Singh, P. K., & Kumar, A. (2015) · PLoS ONE · doi:10.1371/journal.pone.0119541 · Cited by 44
Oksala, N., Pärssinen, J., Seppälä, I., Raitoharju, E., Kholová, I., Hernesniemi, J. A., Lyytikäinen, L., Levula, M., Mäkelä, K.-M., Sioris, T., et al. (2013) · Circulation Cardiovascular Genetics · doi:10.1161/circgenetics.113.000141 · Cited by 43
RIG-1 receptor expression in the pathology of Alzheimer’s disease
de Rivero Vaccari, J. P., Brand, F. J., Sedaghat, C., Mash, D. C., Dietrich, W. D., & Keane, R. W. (2014) · Journal of Neuroinflammation · doi:10.1186/1742-2094-11-67 · Cited by 43
Protein modification by aldehydophospholipids and its functional consequences
Stemmer, U., & Hermetter, A. (2012) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2012.03.006 · Cited by 43
Atherosclerosis—Multiple Pathways to Lesional Macrophages
Schulz, C., & Maßberg, S. (2014) · Science Translational Medicine · doi:10.1126/scitranslmed.3008922 · Cited by 43
IRAK1 mediates TLR4-induced ABCA1 downregulation and lipid accumulation in VSMCs
Guo, L., Chen, C.-H., Zhang, L., Cao, X.-J., Ql, M., Deng, P., Zhu, G., Gao, C.-Y., Li, B.-H., Pi, Y., et al. (2015) · Cell Death and Disease · doi:10.1038/cddis.2015.212 · Cited by 43
Modified phospholipids as anti-inflammatory compounds
Feige, E., Mendel, I., George, J., Yacov, N., & Harats, D. (2010) · Current Opinion in Lipidology · doi:10.1097/mol.0b013e32833f2fcb · Cited by 43
Zhu, L., Li, R., Jiao, S., Wei, J., Yan, Y., Wang, Z. A., Li, J., & Du, Y. (2020) · Marine Drugs · doi:10.3390/md18100488 · Cited by 44
Neuroinflammation in Alzheimer's disease and beneficial action of luteolin
Delgado, A., Cholevas, C., & Theoharides, T. C. (2021) · BioFactors · doi:10.1002/biof.1714 · Cited by 48
Reich, N., & Hölscher, C. (2024) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2024.101122 · Cited by 43
Ovulation as danger signaling event of innate immunity
Spanel‐Borowski, K. (2010) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2010.12.008 · Cited by 43
Michalska, P., Mayo, P., Fernández‐Mendívil, C., Tenti, G., Duarte, P., Buendía, I., Ramos, M. T., López, M. G., Menéndez, J. C., & Leon, R. M. (2020) · Antioxidants · doi:10.3390/antiox9080650 · Cited by 42
The microglial lysosomal system in Alzheimer’s disease: Guardian against proteinopathy
Van Acker, Z. P., Perdok, A., Bretou, M., & Annaert, W. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101444 · Cited by 45
Two Faces of Macrophages: Training and Tolerance
Zubair, K., You, C., Kwon, G., & Kang, K. (2021) · Biomedicines · doi:10.3390/biomedicines9111596 · Cited by 47
Yang, B., Hang, S., Xu, S., Gao, Y., Yu, W., Zang, G., Zhang, L., & Wang, Z. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e32073 · Cited by 46
The role of the inflammasome in cardiovascular diseases
Li, X., Deroide, N., & Mallat, Z. (2014) · Journal of Molecular Medicine · doi:10.1007/s00109-014-1144-3 · Cited by 43
Ishibashi, M., Sayers, S., D'Armiento, J. M., Tall, A. R., & Welch, C. L. (2013) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2013.03.035 · Cited by 41
Terrill, S. E., Mohan, M. J., & Nichols, M. R. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2014.08.001 · Cited by 42
Treating atherosclerosis: the potential of Toll-like receptors as therapeutic targets
Cole, J. E., Mitra, A. T., & Monaco, C. G. (2010) · Expert Review of Cardiovascular Therapy · doi:10.1586/erc.10.149 · Cited by 40
Karper, J. C., de Vries, M. R., van den Brand, B. T., Hoefer, I. E., Fischer, J. W., Jukema, J. W., Niessen, H. W. M., & Quax, P. H. A. (2011) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.111.223271 · Cited by 40
Zhang, H., Zhai, Z., Zhou, H., Li, Y., Li, X., Lin, Y., Li, W., Shi, Y., & Zhou, M.-S. (2015) · BioMed Research International · doi:10.1155/2015/403616 · Cited by 41
Olonisakin, T. F., Li, H., Xiong, Z., Kochman, E. J. K., Yu, M., Qu, Y., Hulver, M., Kolls, J. K., Croix, C. M. S., Doi, Y., et al. (2016) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiw451 · Cited by 42
Dabo, S., Maillard, P., Rodríguez, M. C., Hansen, M. D., Mazouz, S., Bigot, D.-J., Tible, M., Janvier, G., Helynck, O., Cassonnet, P., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-16089-8 · Cited by 41
Neuroinflammation in Alzheimer’s Disease: Microglia, Molecular Participants and Therapeutic Choices
Wang, H., Shen, Y., Chuang, H.-Y., Chiu, C., Ye, Y., & Zhao, L. (2019) · Current Alzheimer Research · doi:10.2174/1567205016666190503151648 · Cited by 43
Ayton, S., Janelidze, S., Roberts, B. R., Palmqvist, S., Kalinowski, P., Diouf, I., Belaidi, A. A., Stomrud, E., Bush, A. I., & Hansson, O. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101904 · Cited by 43
Tajbakhsh, A., Read, M. I., Barreto, G. E., Ávila-Rodriguez, M., Hayat, S. M. G., & Sahebkar, A. (2021) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2021.173873 · Cited by 41
A Chemical Proteomic Map of Heme–Protein Interactions
Homan, R. A., Jadhav, A. M., Conway, L. P., & Parker, C. G. (2022) · Journal of the American Chemical Society · doi:10.1021/jacs.2c06104 · Cited by 43
Lack of the scavenger receptor CD 36 alters microglial phenotypes after neonatal stroke
Li, F., Faustino, J. V., Woo, M., Derugin, N., & Vexler, Z. S. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13239 · Cited by 44
Yahaya, M. A. F., Bakar, A. R. A., Stanslas, J., Nordin, N. N. M., Zainol, M., & Mehat, M. Z. (2021) · BMC Biotechnology · doi:10.1186/s12896-021-00697-4 · Cited by 40
Chen, C., Ai, Q., Shi, A., Wang, N., Wang, L., & Wei, Y. (2022) · Nutritional Neuroscience · doi:10.1080/1028415x.2022.2051957 · Cited by 40
The Role of Colchicine in Atherosclerosis: From Bench to Bedside
González, L., Bulnes, J. F., Paz, O. M., Venturelli, P. M., & Martı́nez-Rodrı́guez, G. (2022) · Pharmaceutics · doi:10.3390/pharmaceutics14071395 · Cited by 42
Yorkie Regulates Neurodegeneration Through Canonical Pathway and Innate Immune Response
Dubey, S. K., & Tapadia, M. G. (2017) · Molecular Neurobiology · doi:10.1007/s12035-017-0388-7 · Cited by 38
Holen, E., Araujo, P. W., Sissener, N. H., Rosenlund, G., & Waagbø, R. (2017) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2017.10.040 · Cited by 40
Hao, D., Danbin, W., Maojuan, G., Chun, S., Bin, L., Yang, L., Yingxin, S., Guanwei, F., Chen, Y., Gao, Q., et al. (2019) · Pharmacological Research · doi:10.1016/j.phrs.2019.104306 · Cited by 40
Functional consequences of CD36 downregulation by TLR signals
Zamora, C., Cantó, E., Nieto, J. C., Ortiz, M. A., Juárez, C., & Vidal, S. (2012) · Cytokine · doi:10.1016/j.cyto.2012.06.020 · Cited by 41
Gusev, E., Sarapultsev, A., Hu, D., & Черешнев, В. А. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22147582 · Cited by 42
Small-Molecule Modulators Targeting Toll-like Receptors for Potential Anticancer Therapeutics
Wang, J., Zhang, J., Wang, J., Hu, X., Ouyang, L., & Wang, Y. (2023) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.2c01655 · Cited by 39
Modulation of innate immunity by African Trypanosomes
Paulnock, D. M., Freeman, B. E., & Mansfield, J. M. (2010) · Parasitology · doi:10.1017/s0031182010001460 · Cited by 41
Chung, Y., Kim, D.-H., & Lee, W. (2016) · Scientific Reports · doi:10.1038/srep34533 · Cited by 39
Xia, M., Zhao, Q., Zhang, H., Chen, Y., Yuan, Z., Xu, Y., & Zhang, M. (2017) · Neural Plasticity · doi:10.1155/2017/6237351 · Cited by 39
Tabares-Guevara, J. H., Lara-Guzmán, O. J., Londoño‐Londoño, J., Sierra, J. A., León-Varela, Y. M., Álvarez, R., Osorio, E., & Ramírez‐Pineda, J. R. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00923 · Cited by 42
Vozenilek, A. E., Navratil, A. R., Green, J. M., Coleman, D. T., Blackburn, C. M. R., Finney, A. C., Pearson, B. H., Chrast, R., Finck, B. N., Klein, R. L., et al. (2017) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.117.310455 · Cited by 37
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Yang, T., Zhu, Z., Yin, E., Wang, Y., Zhang, C., Yuan, H., Zhang, H., Jin, S., Guo, Z., & Wang, X. (2019) · Chemical Science · doi:10.1039/c9sc03042e · Cited by 38
Yan, Y., Song, D., Wu, J., & Wang, J. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00024 · Cited by 42
Richards, M. R., Black, A. S., Bonnet, D. J., Barish, G. D., Woo, C. W., Tabas, I. A., Curtiss, L. K., & Tobias, P. S. (2012) · Innate Immunity · doi:10.1177/1753425912447130 · Cited by 39
Zernecke, A. (2012) · Thrombosis and Haemostasis · doi:10.1160/th11-08-0603 · Cited by 38
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Biological and pathophysiological roles of end-products of DHA oxidation
Yakubenko, V. P., & Byzova, T. V. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2016.09.022 · Cited by 39
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Chistiakov, D. A., Melnichenko, A. А., Orekhov, A. N., & Bobryshev, Y. V. (2016) · International Journal of Cardiology · doi:10.1016/j.ijcard.2016.12.164 · Cited by 39
Puttalingaiah, R. T., Wu, X., Gowda, K., Punnath, K., Neelgund, S. E., Febbraio, M., & Gowda, D. C. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.781294 · Cited by 41
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Oliveira, B. C. D. L., Bellozi, P. M. Q., Reis, H. J., & de Oliveira, A. C. P. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.02.012 · Cited by 39
Metadata
- Authors
- Stewart, C. R., Stuart, L. M., Wilkinson, K., van Gils, J. M., Deng, J., Halle, A., Rayner, K. J., Boyer, L., Zhong, R., Frazier, W. A., Lacy-Hulbert, A., Khoury, J. E., Golenbock, D. T., & Moore, K. J.
- Affiliations
- Harvard University (US)
- University of Massachusetts Chan Medical School (US)
- Washington University in St. Louis (US)
- Corresponding author
- Moore, Kathryn J
- ORCID
- Venue
- Nature Immunology
- Published
- 2009-12-27
- Volume
- 11
- Issue
- 2
- Pages
- 155-161
- ISSN
- 1529-2908 (ISSN-L)
- 1529-2916
- PMC
- PMC2809046
- OpenAlex
- W2045772297
- Cited by
- 1,513
- References
- 42
- Citations by year
- 2026: 53 · 2025: 69 · 2024: 107 · 2023: 74 · 2022: 108 · 2021: 96 · 2020: 102 · 2019: 97 · 2018: 99 · 2017: 94 · 2016: 98 · 2015: 108 · 2014: 81 · 2013: 92 · 2012: 104
- FWCI
- 33.44
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Immunology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- The Journal of the American Medical Association (JAMA) Network (American Medical Association) (submittedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- Leiden Repository (Leiden University) (submittedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Funders
- Wellcome Trust (068089)
- National Institute on Aging (R01AG20255, R01AG020255, R01AG032349)
- National Institute of Allergy and Infectious Diseases (R01AI079198)
- National Institute of Diabetes and Digestive and Kidney Diseases (P30DK043351)
- National Institute of Neurological Disorders and Stroke (R01NS059005)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Life Sciences › Immunology and Microbiology › Immunology › Atherosclerosis and Cardiovascular Diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
- Keywords
- CD36, TLR4, TLR6, sterile inflammation, oxidized LDL, amyloid-beta, atherosclerosis, Alzheimer's disease, innate immune activation
- MeSH terms
- Animals, Cell Line, Humans, Inflammation, Lipoproteins, LDL, Mice, Inbred C57BL, Blotting, Western, Signal Transduction, Gene Expression, Amyloid beta-Peptides, Microglia, Mice, Knockout, Chemokines, CD36 Antigens, Reverse Transcriptase Polymerase Chain Reaction, Immunoprecipitation, Atherosclerosis, Toll-Like Receptor 4, Toll-Like Receptor 6, Mice
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