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Inefficient clearance of myelin debris by microglia impairs remyelinating processes
Open accessAbstract
An imbalance between remyelinating and demyelinating rates underlies degenerative processes in demyelinating diseases such as multiple sclerosis. An optimal therapeutic strategy would be to stimulate remyelination while limiting demyelination. Although accumulation of myelin debris impairs remyelination, the mechanisms regulating the clearance of such debris by mononuclear phagocytic cells are poorly understood. We demonstrate that after cuprizone intoxication, CCR2-dependent infiltration of mouse bone marrow-derived cells is abundant in demyelinating areas, but that these cells do not impact demyelination. However, in CX3CR1-deficient mice, the clearance of myelin debris by microglia was blocked greatly, affecting the integrity of the axon and myelin sheaths and thus preventing proper remyelination. These results highlight the crucial role played by CX3CR1 in myelin removal and show that there can be no efficient remyelination after a primary demyelinating insult if myelin clearance by microglia is impaired.
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“Mounting evidence suggests that microglia, which are the professional phagocytes of the CNS, are critically involved in ensuring the proper containment and removal of neurotoxic material in neurodegenerative disease pathogenesis (Condello et al., 2015; Hickman et al., 2018; Lampron et al., 2015).”
From SYK coordinates neuroprotective microglial responses in neurodegenerative disease (2022) · cites this paper as Lampron et al., 2015
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“Cessation of cuprizone leads to subsequent remyelination, and clearance of myelin debris is believed to be crucial for remyelination and recovery [5,6].”
From Multifaceted response of microglia in the cuprizone model of demyelination (2026) · cites this paper as [5]
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“Microglia also clear myelin debris, and secrete trophic factors to promote oligodendrocyte growth and survival [5,11,12].”
From Multifaceted response of microglia in the cuprizone model of demyelination (2026) · cites this paper as [5]
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“indicating that microglial clearance of myelin debris continues following cuprizone withdrawal, as reported in previous studies [3,5].”
From Multifaceted response of microglia in the cuprizone model of demyelination (2026) · cites this paper as [5]
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“Accumulation of debris within lesions has been demonstrated to inhibit oligodendrocyte recruitment and differentiation (18, 41, 44) and, thus, delay recovery/remyelination.”
From Microglia depletion exacerbates demyelination and impairs remyelination in a neurotropic coronavirus infection (2020) · cites this paper as [44]
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“Long-term demyelination occurs post-SCI, with lipid-containing myelin debris being absorbed and processed by inflammatory cells, including microglia—a process crucial for paving the way for regenerative reactions and inflammation resolution [9–11].”
From miR-223 accelerates lipid droplets clearance in microglia following spinal cord injury by upregulating ABCA1 (2024) · cites this paper as [10]
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“Efficient myelin debris removal and clearance by phagocytic cells are critical to eliminate inhibitory signals interfering with OPC activation, recruitment to the site of demyelination and/or differentiation into myelinating mature OLs [14, 26, 27].”
From TREM2 activation on microglia promotes myelin debris clearance and remyelination in a model of multiple sclerosis (2020) · cites this paper as [27]
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“Recruited cell populations included monocytes and lymphocytes.”
From Cuprizone‐induced demyelination triggers a CD8‐pronounced T cell recruitment (2021) · cites this paper as Lampron et al., 2015
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“In line with our observation, Lampron and colleagues demonstrated a significant infiltration of transplanted GFP-expressing bone-marrow cells into the CNS, with a peak of infiltration at weeks 4 and 5 of intoxication (Lampron et al., 2015).”
From Cuprizone‐induced demyelination triggers a CD8‐pronounced T cell recruitment (2021) · cites this paper as Lampron et al., 2015
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“When CCR2 -/-instead of CCR2 +/+ bone-marrow cells were transplanted, infiltration into the CNS was almost completely blocked without affecting the extent of cuprizoneinduced demyelination.”
From Cuprizone‐induced demyelination triggers a CD8‐pronounced T cell recruitment (2021) · cites this paper as Lampron et al., 2015
In the citing paper
“Activated microglia within the demyelinating areas of CPZ lesions express various cytokines, chemokines and growth factors (21, 22), and inefficient clearance of myelin debris by microglia impairs remyelinating processes in the CPZ model (23).”
From Absence of miRNA-146a Differentially Alters Microglia Function and Proteome (2020) · cites this paper as [23]
In the citing paper
“Thus, removal of myelin debris by microglia is important for oligodendrocyte proliferation and stimulation of remyelination, which can be achieved with a neuroprotective microglial phenotype (Lampron et al. 2015).”
From MiR-124 and MiR-155 as Therapeutic Targets in Microglia-Mediated Inflammation in Multiple Sclerosis (2025) · cites this paper as Lampron et al. 2015
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Citations
Cites
NIH Image to ImageJ: 25 years of image analysis
Schneider, C. A., Rasband, W. S., & Eliceiri, K. W. (2012) · Nature Methods · doi:10.1038/nmeth.2089 · Cited by 64,638
Fate Mapping Analysis Reveals That Adult Microglia Derive from Primitive Macrophages
Ginhoux, F., Greter, M., Leboeuf, M., Nandi, S., See, P., Gokhan, S., Mehler, M. F., Conway, S. J., Ng, L. G., Stanley, E. R., et al. (2010) · Science · doi:10.1126/science.1194637 · Cited by 5,175
New Multiple Sclerosis Phenotypic Classification
LUBLIN, F. D. (2014) · European Neurology · doi:10.1159/000367614 · Cited by 4,277
Axonal transection in the lesions of multiple sclerosis
Trapp, B. D., Peterson, J., Ransohoff, R. M., Rudick, R., Mörk, S., & Bö, L. (1998) · New England Journal of Medicine · doi:10.1056/nejm199801293380502 · Cited by 4,029
Defining the clinical course of multiple sclerosis
LUBLIN, F. D., & Reingold, S. C. (1996) · Neurology · doi:10.1212/wnl.46.4.907 · Cited by 3,762
Defining the clinical course of multiple sclerosis: The 2013 revisions
Lublin, F. D., Reingold, S. C., Cohen, J. A., Cutter, G. R., Sørensen, P. S., Thompson, A. J., Wolinsky, J. S., Balcer, L. J., Banwell, B., Barkhof, F., et al. (2014) · Neurology · doi:10.1212/wnl.0000000000000560 · Cited by 3,177
Development of Monocytes, Macrophages, and Dendritic Cells
Geissmann, F., Manz, M. G., Jung, S., Sieweke, M. H., Merad, M., & Ley, K. (2010) · Science · doi:10.1126/science.1178331 · Cited by 3,049
The use of the elevated plus maze as an assay of anxiety-related behavior in rodents
Walf, A. A., & Frye, C. A. (2007) · Nature Protocols · doi:10.1038/nprot.2007.44 · Cited by 3,035
The use of a plus-maze to measure anxiety in the mouse
Lister, R. G. (1987) · Psychopharmacology · doi:10.1007/bf00177912 · Cited by 2,617
A Lineage of Myeloid Cells Independent of Myb and Hematopoietic Stem Cells
Schulz, C., Perdiguero, E. G., Chorro, L., Szabo-Rogers, H., Cagnard, N., Kierdorf, K., Prinz, M., Wu, B., Jacobsen, S. E. W., Pollard, J. W., et al. (2012) · Science · doi:10.1126/science.1219179 · Cited by 2,578
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CNS-localized myeloid cells capture living invading T cells during neuroinflammation
Wasser, B., Luchtman, D. W., Löffel, J. T., Robohm, K., Birkner, K., Stroh, A., Vogelaar, C. F., Zipp, F., & Bittner, S. (2020) · The Journal of Experimental Medicine · doi:10.1084/jem.20190812 · Cited by 38
Fractalkine enhances oligodendrocyte regeneration and remyelination in a demyelination mouse model
de Almeida, M. M. A., Watson, A. E. S., Bibi, S., Dittmann, N. L., Goodkey, K., Sharafodinzadeh, P., Galleguillos, D., Nakhaei‐Nejad, M., Kosaraju, J., Steinberg, N., et al. (2023) · Stem Cell Reports · doi:10.1016/j.stemcr.2022.12.001 · Cited by 36
Role of Microglial Cells in the Pathophysiology of MS: Synergistic or Antagonistic?
Mado, H., Adamczyk-Sowa, M. H., & Sowa, P. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24031861 · Cited by 43
Absence of miRNA-146a Differentially Alters Microglia Function and Proteome
Martin, N. A., Hyrlov, K. H., Elkjaer, M. L., Thygesen, E. K., Wlodarczyk, A., Elbaek, K. J., Aboo, C., Okarmus, J., Benedikz, E., Reynolds, R., et al. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01110 · Cited by 36
Endogenous neural stem cells modulate microglia and protect against demyelination
Brousse, B., Mercier, O., Magalon, K., Daian, F., Durbec, P., & Cayre, M. (2021) · Stem Cell Reports · doi:10.1016/j.stemcr.2021.05.002 · Cited by 38
The Glial Cells Respond to Spinal Cord Injury
Wang, R., Zhou, R., Chen, Z., Gao, S., & Zhou, F. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.844497 · Cited by 35
Glial Cells as Key Regulators in Neuroinflammatory Mechanisms Associated with Multiple Sclerosis
Theophanous, S., Sargiannidou, I., & Kleopa, K. A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25179588 · Cited by 38
Drake, S., Zaman, A., Gianfelice, C., Hua, E. M.-L., Heale, K., Afanasiev, E., Klément, W., Stratton, J. A., Prat, A., Zandee, S., et al. (2024) · Journal of Neuroinflammation · doi:10.1186/s12974-024-03278-2 · Cited by 38
Cellular and Molecular Mechanisms Underpinning Macrophage Activation during Remyelination
Lloyd, A. F., & Miron, V. E. (2016) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2016.00060 · Cited by 37
Microglia: Senescence Impairs Clearance of Myelin Debris
Thériault, P., & Rivest, S. (2016) · Current Biology · doi:10.1016/j.cub.2016.06.066 · Cited by 37
Specialized functions of resident macrophages in brain and heart
Nicolás-Ávila, J. Á., Hidalgo, A., & Ballesteros, I. (2018) · Journal of Leukocyte Biology · doi:10.1002/jlb.6mr0118-041r · Cited by 36
New therapeutic avenues of MCSF for brain diseases and injuries
Pons, V., & Rivest, S. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00499 · Cited by 35
Self-citationSen, M. K., Almuslehi, M. S. M., Gyengesi, E., Myers, S. J., Shortland, P. J., Mahns, D. A., & Coorssen, J. R. (2019) · Cells · doi:10.3390/cells8111314 · Cited by 35
Dietary influence on central nervous system myelin production, injury, and regeneration
Langley, M. R., Triplet, E. M., & Scarisbrick, I. A. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2020.165779 · Cited by 35
Giacometti, J., & Kezele, T. G. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/6125638 · Cited by 35
Lee, J., Villarreal, O. D., Chen, X., Zandee, S., Young, Y. K., Torok, C., Lamarche-Vane, N., Prat, A., Rivest, S., Gosselin, D., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108560 · Cited by 38
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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 36
Rajasundaram, S. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00402 · Cited by 37
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Yin, J.-J., He, Y., An, J., Miao, Q., Sui, R., Wang, Q., Yu, J., Xiao, B., & Ma, C. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00572 · Cited by 35
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Watson, A. E. S., de Almeida, M. M. A., Dittmann, N. L., Li, Y., Torabi, P., Footz, T. K., Vetere, G., Galleguillos, D., Sipione, S., Cardona, A. E., et al. (2021) · Stem Cell Reports · doi:10.1016/j.stemcr.2021.06.010 · Cited by 34
Clemastine Induces an Impairment in Developmental Myelination
Palma, A., Chara, J. C., Montilla, A., Otxoa-de-Amezaga, A., Ruíz-Jaén, F., Planas, A. M., Matute, C., Pérez‐Samartín, A., & Domercq, M. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.841548 · Cited by 35
Li, W., Meng, X., Peng, K., Han, Y., Liu, H., Zhao, W., Wang, G., Deng, L., Liu, H., Li, Z., et al. (2023) · Advanced Science · doi:10.1002/advs.202305989 · Cited by 36
Scott‐Hewitt, N., Folts, C. J., Hogestyn, J. M., Piester, G., Mayer-Pröschel, M., & Noble, M. (2017) · Human Molecular Genetics · doi:10.1093/hmg/ddx153 · Cited by 32
Qki is an essential regulator of microglial phagocytosis in demyelination
Ren, J., Dai, C., Zhou, X., Barnes, J. A., Chen, X., Wang, Y., Yuan, L., Shingu, T., Heimberger, A. B., Chen, Y., et al. (2021) · Journal of Experimental Medicine · doi:10.1084/jem.20190348 · Cited by 36
Verden, D. R., & Macklin, W. B. (2016) · Journal of Neuroscience Research · doi:10.1002/jnr.23923 · Cited by 33
Liang, J., Li, N., Zhang, Y., Hou, C., Yang, X., Shimizu, T., Wang, X., Ikenaka, K., Fan, K., & Ma, J. (2016) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2016.00152 · Cited by 34
Vanherle, S., Jorissen, W., Dierckx, T., Loix, M., Grajchen, E., Mingneau, F., Guns, J., Gervois, P., Lambrichts, I., Dehairs, J., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111591 · Cited by 31
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Iemmolo, M., Ghersi, G., & Bivona, G. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24098026 · Cited by 35
Liu, Y., Given, K. S., Owens, G. P., Macklin, W. B., & Bennett, J. L. (2018) · Glia · doi:10.1002/glia.23512 · Cited by 34
Involvement of Wnt7a in the role of M2c microglia in neural stem cell oligodendrogenesis
Mecha, M., Yanguas‐Casás, N., Feliú, A., Mestre, L., Carrillo-Salinas, F. J., Riecken, K., Gómez‐Nicola, D., & Guaza, C. (2020) · Journal of Neuroinflammation · doi:10.1186/s12974-020-01734-3 · Cited by 33
Myeloid cell replacement is neuroprotective in chronic experimental autoimmune encephalomyelitis
Mader, M. M.-D., Napole, A., Wu, D., Atkins, M., Scavetti, A., Shibuya, Y., Foltz, A. G., Hahn, O., Yoo, Y., Danziger, R., et al. (2024) · Nature Neuroscience · doi:10.1038/s41593-024-01609-3 · Cited by 32
Lesion-remote astrocytes govern microglia-mediated white matter repair
McCallum, S. E., Suresh, K. B., Islam, T. S., Tripathi, M. K., Saustad, A. W., Shelest, O., Patil, A., Lee, D. S., Kwon, B., Leitholf, K., et al. (2025) · Nature · doi:10.1038/s41586-025-09887-y · Cited by 36
Shimizu, T., Durose, W. W., Li, J., Abe, M., Sakimura, K., Chetsawang, B., Sahara, Y., Tohyama, K., Tanaka, K. F., & Ikenaka, K. (2017) · Glia · doi:10.1002/glia.23134 · Cited by 34
Filho, A. J. M. C., Eyres, C., Blöbaum, L., Landwehr, A., & Tremblay, M. (2024) · Journal of Neurochemistry · doi:10.1111/jnc.16098 · Cited by 33
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Leenders, F., Koole, L., Slaets, H., Tiane, A., van den Hove, D., & Vanmierlo, T. (2024) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2024.111959 · Cited by 30
Ummenthum, K. M. D., Peferoen, L. A. N., Finardi, A., Baker, D., Pryce, G., Mantovani, A., Bsibsi, M., Bottazzi, B., Peferoen-Baert, R. M. B., van der Valk, P., et al. (2015) · European Journal of Immunology · doi:10.1002/eji.201545950 · Cited by 32
Cohen, M., Ben-Yehuda, H., Porat, Z., Rapôso, C., Gordon, S., & Schwartz, M. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.2199-16.2016 · Cited by 31
Microglia as therapeutic targets for central nervous system remyelination
Mahmood, A., & Miron, V. E. (2022) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2022.102188 · Cited by 29
Dong, X., Zhang, Z., Shu, X., Zhuang, Z., Liu, P., Liu, R., Xia, S., Bao, X., Xu, Y., & Chen, Y. (2023) · Neuroscience Bulletin · doi:10.1007/s12264-023-01147-1 · Cited by 30
Myelin debris phagocytosis in demyelinating disease
Gao, R., Song, S., Tian, M., Wang, L., Zhang, Y., & Li, X. (2024) · Glia · doi:10.1002/glia.24602 · Cited by 31
Robinson, R. R., Dietz, A. K., Maroof, A. M., Asmis, R., & Forsthuber, T. G. (2019) · Immunotherapy · doi:10.2217/imt-2018-0153 · Cited by 33
Modulation of Neural Activity for Myelination in the Central Nervous System
Choi, E. H., Blasiak, A., Lee, J., & Yang, I. H. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00952 · Cited by 30
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Pons, V., & Rivest, S. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00284 · Cited by 29
Galloway, D. A., Carew, S. J., Blandford, S. N., Benoit, R. Y., Fudge, N. J., Berry, T., Moore, G. R. W., Barron, J., & Moore, C. S. (2022) · Journal of Neurochemistry · doi:10.1111/jnc.15650 · Cited by 31
Zhou, K. Q., Bennet, L., Wassink, G., McDouall, A., Curtis, M., Highet, B., Stevenson, T. J., Gunn, A., & Davidson, J. O. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-022-02499-7 · Cited by 24
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Rahimian, R., Perlman, K., Canonne, C., & Mechawar, N. (2022) · Drug Discovery Today · doi:10.1016/j.drudis.2022.06.015 · Cited by 32
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Cheung, G., Lin, Y. C., & Papadopoulos, V. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1210205 · Cited by 33
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Tiwari, V., & Simons, M. (2025) · The Journal of Experimental Medicine · doi:10.1084/jem.20241232 · Cited by 39
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Konishi, H., Kiyama, H., & Ueno, M. (2018) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2018.09.009 · Cited by 31
Penkert, H., Bertrand, A., Tiwari, V., Breimann, S., Müller, S. A., Jordan, P. M., Gerl, M. J., Klose, C. D., Cantuti‐Castelvetri, L., Bosch-Queralt, M., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109898 · Cited by 31
Liu, L., Du, X., Yang, Q. K., Li, M., Ran, Q., Liu, Q., Yang, L., Sun, L., Guo, Y., Li, Y., et al. (2022) · Phytomedicine · doi:10.1016/j.phymed.2022.154309 · Cited by 28
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Saha, A., Buntz, S., Scotland, P., Xu, L., Noeldner, P. K., Patel, S. A., Wollish, A., Gunaratne, A., Gentry, T., Troy, J. D., et al. (2016) · JCI Insight · doi:10.1172/jci.insight.86667 · Cited by 28
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Baldassari, L. E., Feng, J. J., Clayton, B. L. L., Oh, S., Sakaie, K., Tesar, P. J., Wang, Y., & Cohen, J. A. (2019) · Expert Review of Neurotherapeutics · doi:10.1080/14737175.2019.1632192 · Cited by 29
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Naghibzadeh, M., Ranjbar, R., Tabandeh, M. R., & Habibi, A. (2018) · International Journal of Sports Medicine · doi:10.1055/a-0608-4635 · Cited by 28
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Sonn, I., Honda‐Ozaki, F., Yoshimatsu, S., Morimoto, S., Watanabe, H., & Okano, H. (2022) · Inflammation and Regeneration · doi:10.1186/s41232-022-00201-1 · Cited by 30
Zhang, Q., Chen, Z., Zhang, K., Zhu, J., & Jin, T. (2023) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14176 · Cited by 27
Meller, J., Chen, Z., Dudiki, T., Cull, R. M., Murtazina, R., Bal, S. K., Pluskota, E., Stefl, S., Plow, E. F., Trapp, B. D., et al. (2017) · JCI Insight · doi:10.1172/jci.insight.93002 · Cited by 27
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Dermitzakis, I., Μanthou, M. E., Meditskou, S., Miliaras, D., Kesidou, E., Boziki, M. K., Petratos, S., Grigoriadis, N., & Theotokis, P. (2022) · Current Issues in Molecular Biology · doi:10.3390/cimb44070222 · Cited by 26
DePaula-Silva, A. B. (2024) · Viruses · doi:10.3390/v16010119 · Cited by 29
Maleki, A. F., Cisbani, G., Plante, M.-M., Préfontaine, P., Laflamme, N., Gosselin, J., & Rivest, S. (2020) · Journal of Neuroinflammation · doi:10.1186/s12974-020-01893-3 · Cited by 26
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Miedema, A., Wijering, M. H. C., Eggen, B. J. L., & Kooistra, S. M. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.583811 · Cited by 24
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de Almeida, M. M. A., Goodkey, K., & Voronova, A. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1130205 · Cited by 26
Pilipović, I., Stojić-Vukanić, Z., Prijić, I., Jasnic, N. I., & Leposavić, G. (2019) · Neurobiology of Disease · doi:10.1016/j.nbd.2019.104665 · Cited by 27
Tarale, P., & Alam, M. M. (2022) · Inflammopharmacology · doi:10.1007/s10787-022-00958-4 · Cited by 26
Role of innate immune cells in multiple sclerosis
Prado, C. E., Herrada, A. A., Hevia, D., Galleguillos, L., & Escobedo, N. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1540263 · Cited by 26
Lubart, A., Benbenishty, A., Har-Gil, H., Laufer, H., Gdalyahu, A., Assaf, Y., & Blinder, P. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa223 · Cited by 26
Blanke, N., Go, V., Rosene, D. L., & Bigio, I. J. (2021) · Neurophotonics · doi:10.1117/1.nph.8.1.015010 · Cited by 24
Having an Old Friend for Dinner: The Interplay between Apoptotic Cells and Efferocytes
Lam, A. L., & Heit, B. (2021) · Cells · doi:10.3390/cells10051265 · Cited by 22
Monocytes in central nervous system remyelination
Forbes, L. H., & Miron, V. E. (2021) · Glia · doi:10.1002/glia.24111 · Cited by 24
T cell–neuron interaction in inflammatory and progressive multiple sclerosis biology
Brummer, T., Zipp, F., & Bittner, S. (2022) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2022.102588 · Cited by 24
Engineering biomaterial microenvironments to promote myelination in the central nervous system
Unal, D. B., Caliari, S. R., & Lampe, K. J. (2019) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2019.07.013 · Cited by 24
Jiang, Y., Armada, K., & Martin, J. H. (2019) · Experimental Neurology · doi:10.1016/j.expneurol.2019.113015 · Cited by 26
Liu, Y., Hammel, G., Shi, M., Cheng, Z., Zivkovic, S., Wang, X., Xu, P., He, X., Guo, B., Ren, Y., et al. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.651827 · Cited by 24
Trem2-deficiency aggravates and accelerates age-related myelin degeneration
McCray, T. J., Bedford, L. M., Bissel, S. J., & Lamb, B. T. (2024) · Acta Neuropathologica Communications · doi:10.1186/s40478-024-01855-3 · Cited by 23
Koeniger, T., & Küerten, S. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18102072 · Cited by 22
Wang, K., Wang, C., Chen, D., Huang, Y., Li, J., Wei, P., Shi, Z., Zhang, Y., & Gao, Y. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04465-1 · Cited by 23
Sun, J., Zhu, K., Wang, Y., Wang, D.-J., Zhang, M.-Z., Sarlus, H., Benito‐Cuesta, I., Zhao, X.-Q., Zou, Z., Zhong, Q.-Y., et al. (2022) · Acta Pharmacologica Sinica · doi:10.1038/s41401-022-01000-7 · Cited by 25
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Olveda, G. E., Barasa, M. N., & Hill, R. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114385 · Cited by 23
Stoolman, J. S., Grant, R. A., Poor, T. A., Weinberg, S. E., D’Alessandro, K. B., Tan, J., Hu, J. Y.-S., Zerrer, M. E., Wood, W. A., Harding, M. C., et al. (2024) · Nature Metabolism · doi:10.1038/s42255-024-01080-1 · Cited by 24
Noble, M., Scott‐Hewitt, N., & Folts, C. J. (2018) · Neural Regeneration Research · doi:10.4103/1673-5374.228712 · Cited by 23
Eshelby’s inclusion theory in light of Noether’s theorem
Federico, S., Alhasadi, M. F., & Grillo, A. (2019) · Mathematics and Mechanics of Complex Systems · doi:10.2140/memocs.2019.7.247 · Cited by 24
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Li, L., & Shi, Y. (2020) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2020.103565 · Cited by 24
Ou, Z., Cheng, Y., Ma, H., Chen, K., Lin, Q., Chen, J., Guo, R., Huang, Z., Cheng, Q., Alaeiilkhchi, N., et al. (2024) · Journal of Translational Medicine · doi:10.1186/s12967-024-05480-5 · Cited by 23
Zhang, G., Yao, Q., Long, C., Yi, P., Song, J., Wu, L., Wan, W., Rao, X., Lin, Y., Wei, G., et al. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-23-01508 · Cited by 25
Maleki, A. F., Cisbani, G., Laflamme, N., Préfontaine, P., Plante, M.-M., Baillargeon, J., Rangachari, M., Gosselin, J., & Rivest, S. (2021) · Neurotherapeutics · doi:10.1007/s13311-020-00998-0 · Cited by 22
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de Andrade, E. G., Ibáñez, F. G., & Tremblay, M. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.839396 · Cited by 22
Marelli, G., Belgiovine, C., Mantovani, A., Erreni, M., & Allavena, P. (2016) · Immunobiology · doi:10.1016/j.imbio.2016.07.013 · Cited by 22
Inhibitory milieu at the multiple sclerosis lesion site and the challenges for remyelination
Galloway, D. A., Gowing, E., Setayeshgar, S., & Kothary, R. (2019) · Glia · doi:10.1002/glia.23711 · Cited by 23
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He, Y., An, J., Yin, J.-J., Sui, R., Miao, Q., Ding, Z., Han, Q.-X., Wang, Q., Ma, C., & Xiao, B. (2019) · International Immunopharmacology · doi:10.1016/j.intimp.2019.105929 · Cited by 22
Ozsvár, A., Szipöcs, R., Ozsvár, Z., Baka, J., Barzó, P., Tamás, G., & Molnár, G. (2018) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2018.01.003 · Cited by 24
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Carden, T. R., Correale, J. D., Pasquini, J. M., & Pérez, M. J. (2019) · Molecular Neurobiology · doi:10.1007/s12035-019-1519-0 · Cited by 21
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Yoon, H., Choi, C., Triplet, E. M., Langley, M. R., Kleppe, L. S., Kim, H. N., Simon, W. L., & Scarisbrick, I. A. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.2029-19.2019 · Cited by 22
Metadata
- Authors
- Lampron, A., Larochelle, A., Laflamme, N., Préfontaine, P., Plante, M.-M., Sánchez, M. G., Yong, V. W., Stys, P. K., Tremblay, M.-È., & Rivest, S.
- Affiliations
- Université Laval (CA)
- University of Calgary (CA)
- Corresponding author
- Rivest, Serge
- ORCID
- Venue
- Journal of Experimental Medicine
- Publisher
- Rockefeller University Press
- Published
- 2015-03-16
- Volume
- 212
- Issue
- 4
- Pages
- 481-495
- ISSN
- 0022-1007 (ISSN-L)
- 1540-9538
- PMC
- PMC4387282
- OpenAlex
- W2096423240
- Cited by
- 595
- References
- 77
- Citations by year
- 2026: 45 · 2025: 42 · 2024: 46 · 2023: 78 · 2022: 86 · 2021: 55 · 2020: 60 · 2019: 61 · 2018: 44 · 2017: 38 · 2016: 29 · 2015: 11
- FWCI
- 32.27
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- cc-by-nc-sa
- Locations
- The Journal of Experimental Medicine (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion, cc-by-nc-sa)
- PubMed (publishedVersion)
- Funders
- Canadian Institutes of Health Research
- Topics
- Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- remyelination, myelin debris clearance, microglia, CX3CR1, CCR2, demyelination, multiple sclerosis, cuprizone, bone marrow-derived cells, axon integrity
- MeSH terms
- CX3C Chemokine Receptor 1, Animals, Axons, Bone Marrow Cells, Demyelinating Diseases, Myelin Sheath, Phagocytes, Microglia, Mice, Knockout, Receptors, Chemokine, Mice, Receptors, CCR2
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