Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/39299
Title: Microglia regulate central nervous system myelin growth and integrity
Authors: McNamara, Niamh B. B.
Munro, David A. D.
Bestard-Cuche, Nadine
Uyeda, Akiko
BOGIE, Jeroen 
Hoffmann, Alana
Holloway, Rebecca K. K.
Molina-Gonzalez, Irene
Askew, Katharine E. E.
Mitchell, Stephen
Mungall, William
Dodds, Michael
Dittmayer, Carsten
Moss, Jonathan
Rose, Jamie
Szymkowiak, Stefan
Amann, Lukas
McColl, Barry W. W.
Prinz, Marco
Spires-Jones, Tara L. L.
Stenzel, Werner
Horsburgh, Karen
HENDRIKS, Jerome 
Pridans, Clare
Muramatsu, Rieko
Williams, Anna
Priller, Josef
Miron, Veronique E. E.
Issue Date: 2022
Publisher: NATURE PORTFOLIO
Source: NATURE, 613 , p. 120 -129
Abstract: Myelin is required for the function of neuronal axons in the central nervous system, but the mechanisms that support myelin health are unclear. Although macrophages in the central nervous system have been implicated in myelin health(1), it is unknown which macrophage populations are involved and which aspects they influence. Here we show that resident microglia are crucial for the maintenance of myelin health in adulthood in both mice and humans. We demonstrate that microglia are dispensable for developmental myelin ensheathment. However, they are required for subsequent regulation of myelin growth and associated cognitive function, and for preservation of myelin integrity by preventing its degeneration. We show that loss of myelin health due to the absence of microglia is associated with the appearance of a myelinating oligodendrocyte state with altered lipid metabolism. Moreover, this mechanism is regulated through disruption of the TGF beta 1-TGF beta R1 axis. Our findings highlight microglia as promising therapeutic targets for conditions in which myelin growth and integrity are dysregulated, such as in ageing and neurodegenerative disease(2,3).
Notes: Miron, VE (corresponding author), Univ Edinburgh, UK Dementia Res Inst, Edinburgh, Scotland.; Miron, VE (corresponding author), Univ Edinburgh, Ctr Discovery Brain Sci, Chancellors Bldg, Edinburgh, Scotland.; Miron, VE (corresponding author), Univ Edinburgh, Queens Med Res Inst, Med Res Council, Ctr Reprod Hlth, Edinburgh, Scotland.; Miron, VE (corresponding author), St Michaels Hosp, Barlo Multiple Sclerosis Ctr, Toronto, ON, Canada.; Miron, VE (corresponding author), St Michaels Hosp, Keenan Res Ctr Biomed Sci, Toronto, ON, Canada.; Miron, VE (corresponding author), Univ Toronto, Dept Immunol, Toronto, ON, Canada.
Veronique.Miron@unityhealth.to
Keywords: Humans;Mice;Animals;Adult;Microglia;Central Nervous System;Axons;Oligodendroglia;Myelin Sheath;Neurodegenerative Diseases
Document URI: http://hdl.handle.net/1942/39299
ISSN: 0028-0836
e-ISSN: 1476-4687
DOI: 10.1038/s41586-022-05534-y
ISI #: 000905304600002
Rights: Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
Category: A1
Type: Journal Contribution
Appears in Collections:Research publications

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