Microglia regulate central nervous system myelin growth and integrity

Niamh B. McNamara(MRC Centre for Reproductive Health), David A. D. Munro(UK Dementia Research Institute), Nadine Bestard-Cuche(MRC Centre for Regenerative Medicine), Akiko Uyeda(National Center of Neurology and Psychiatry), Jeroen F. J. Bogie(Hasselt University), Alana Hoffmann(MRC Centre for Reproductive Health), R. Holloway(St. Michael's Hospital), Irene Molina-González(MRC Centre for Reproductive Health), Katharine E. Askew(University of Edinburgh), Stephen Mitchell(Wellcome Centre for Cell Biology), William Mungall(University of Edinburgh), Michael Dodds(University of Edinburgh), Carsten Dittmayer(Charité - Universitätsmedizin Berlin), Jonathan Moss(MRC Centre for Regenerative Medicine), Jamie Rose(UK Dementia Research Institute), Stefan Szymkowiak(UK Dementia Research Institute), Lukas Amann(University of Freiburg), Barry W. McColl(UK Dementia Research Institute), Marco Prinz(University of Freiburg), Tara L. Spires‐Jones(UK Dementia Research Institute), Werner Stenzel(Charité - Universitätsmedizin Berlin), Karen Horsburgh(University of Edinburgh), Jerome J. A. Hendriks(Hasselt University), Clare Pridans(Maxwell Institute for Mathematical Sciences), Rieko Muramatsu(National Center of Neurology and Psychiatry), Anna Williams(MRC Centre for Regenerative Medicine), Josef Priller(TUM Klinikum), Véronique E. Miron(St. Michael's Hospital)
Nature
December 14, 2022
Cited by 463Open Access
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Abstract

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 TGFβ1–TGFβR1 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 .


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