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Microglia regulate central nervous system myelin growth and integrity.
McNamara, Niamh B; Munro, David A D; Bestard-Cuche, Nadine; Uyeda, Akiko; Bogie, Jeroen F J; Hoffmann, Alana; Holloway, Rebecca K; Molina-Gonzalez, Irene; Askew, Katharine E; Mitchell, Stephen; Mungall, William; Dodds, Michael; Dittmayer, Carsten; Moss, Jonathan; Rose, Jamie; Szymkowiak, Stefan; Amann, Lukas; McColl, Barry W; Prinz, Marco; Spires-Jones, Tara L; Stenzel, Werner; Horsburgh, Karen; Hendriks, Jerome J A; Pridans, Clare; Muramatsu, Rieko; Williams, Anna; Priller, Josef; Miron, Veronique E.
  • McNamara NB; UK Dementia Research Institute at The University of Edinburgh, Edinburgh, UK.
  • Munro DAD; Centre for Discovery Brain Sciences, Chancellor's Building, The University of Edinburgh, Edinburgh, UK.
  • Bestard-Cuche N; Medical Research Council Centre for Reproductive Health, The Queen's Medical Research Institute, The University of Edinburgh, Edinburgh, UK.
  • Uyeda A; UK Dementia Research Institute at The University of Edinburgh, Edinburgh, UK.
  • Bogie JFJ; Centre for Clinical Brain Sciences, Chancellor's Building, The University of Edinburgh, Edinburgh, UK.
  • Hoffmann A; Centre for Regenerative Medicine, Institute for Regeneration and Repair, The University of Edinburgh, Edinburgh, UK.
  • Holloway RK; Departments of Molecular Pharmacology, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Kodaira, Japan.
  • Molina-Gonzalez I; Department of Immunology and Infection, Biomedical Research Institute, Hasselt University, Hasselt, Belgium.
  • Askew KE; University MS Centre, Hasselt University, Hasselt, Belgium.
  • Mitchell S; UK Dementia Research Institute at The University of Edinburgh, Edinburgh, UK.
  • Mungall W; Centre for Discovery Brain Sciences, Chancellor's Building, The University of Edinburgh, Edinburgh, UK.
  • Dodds M; Medical Research Council Centre for Reproductive Health, The Queen's Medical Research Institute, The University of Edinburgh, Edinburgh, UK.
  • Dittmayer C; UK Dementia Research Institute at The University of Edinburgh, Edinburgh, UK.
  • Moss J; Centre for Discovery Brain Sciences, Chancellor's Building, The University of Edinburgh, Edinburgh, UK.
  • Rose J; Medical Research Council Centre for Reproductive Health, The Queen's Medical Research Institute, The University of Edinburgh, Edinburgh, UK.
  • Szymkowiak S; Barlo Multiple Sclerosis Centre, St Michael's Hospital, Toronto, Ontario, Canada.
  • Amann L; Keenan Research Centre for Biomedical Science, St Michael's Hospital, Toronto, Ontario, Canada.
  • McColl BW; Department of Immunology, The University of Toronto, Toronto, Ontario, Canada.
  • Prinz M; UK Dementia Research Institute at The University of Edinburgh, Edinburgh, UK.
  • Spires-Jones TL; Centre for Discovery Brain Sciences, Chancellor's Building, The University of Edinburgh, Edinburgh, UK.
  • Stenzel W; Medical Research Council Centre for Reproductive Health, The Queen's Medical Research Institute, The University of Edinburgh, Edinburgh, UK.
  • Horsburgh K; Centre for Discovery Brain Sciences, Chancellor's Building, The University of Edinburgh, Edinburgh, UK.
  • Hendriks JJA; Wellcome Trust Centre for Cell Biology, King's Buildings, The University of Edinburgh, Edinburgh, UK.
  • Pridans C; Biological and Veterinary Services, Chancellor's Building, The University of Edinburgh, Edinburgh, UK.
  • Muramatsu R; Biological and Veterinary Services, Chancellor's Building, The University of Edinburgh, Edinburgh, UK.
  • Williams A; Department of Neuropathology and Neurocure Clinical Research Center, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Priller J; Centre for Regenerative Medicine, Institute for Regeneration and Repair, The University of Edinburgh, Edinburgh, UK.
  • Miron VE; UK Dementia Research Institute at The University of Edinburgh, Edinburgh, UK.
Nature ; 613(7942): 120-129, 2023 01.
Article en En | MEDLINE | ID: mdl-36517604
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 health1, 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 TGFß1-TGFßR1 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 disease2,3.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Sistema Nervioso Central / Microglía / Vaina de Mielina Límite: Adult / Animals / Humans Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Sistema Nervioso Central / Microglía / Vaina de Mielina Límite: Adult / Animals / Humans Idioma: En Año: 2023 Tipo del documento: Article