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A MAC2-positive progenitor-like microglial population is resistant to CSF1R inhibition in adult mouse brain.
Zhan, Lihong; Fan, Li; Kodama, Lay; Sohn, Peter Dongmin; Wong, Man Ying; Mousa, Gergey Alzaem; Zhou, Yungui; Li, Yaqiao; Gan, Li.
Affiliation
  • Zhan L; Gladstone Institute of Neurological Diseases, San Francisco, United States.
  • Fan L; Helen and Robert Appel Alzheimer's Disease Institute, Brain and Mind Research Institute, Weill Cornell Medicine, New York, United States.
  • Kodama L; Gladstone Institute of Neurological Diseases, San Francisco, United States.
  • Sohn PD; Helen and Robert Appel Alzheimer's Disease Institute, Brain and Mind Research Institute, Weill Cornell Medicine, New York, United States.
  • Wong MY; Neuroscience Graduate Program, University of California, San Francisco, San Francisco, United States.
  • Mousa GA; Medical Scientist Training Program, University of California at San Francisco, San Francisco, United States.
  • Zhou Y; Gladstone Institute of Neurological Diseases, San Francisco, United States.
  • Li Y; Helen and Robert Appel Alzheimer's Disease Institute, Brain and Mind Research Institute, Weill Cornell Medicine, New York, United States.
  • Gan L; Helen and Robert Appel Alzheimer's Disease Institute, Brain and Mind Research Institute, Weill Cornell Medicine, New York, United States.
Elife ; 92020 10 15.
Article de En | MEDLINE | ID: mdl-33054973
Microglia are the resident myeloid cells in the central nervous system (CNS). The majority of microglia rely on CSF1R signaling for survival. However, a small subset of microglia in mouse brains can survive without CSF1R signaling and reestablish the microglial homeostatic population after CSF1R signaling returns. Using single-cell transcriptomic analysis, we characterized the heterogeneous microglial populations under CSF1R inhibition, including microglia with reduced homeostatic markers and elevated markers of inflammatory chemokines and proliferation. Importantly, MAC2/Lgals3 was upregulated under CSF1R inhibition, and shared striking similarities with microglial progenitors in the yolk sac and immature microglia in early embryos. Lineage-tracing studies revealed that these MAC2+ cells were of microglial origin. MAC2+ microglia were also present in non-treated adult mouse brains and exhibited immature transcriptomic signatures indistinguishable from those that survived CSF1R inhibition, supporting the notion that MAC2+ progenitor-like cells are present among adult microglia.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Encéphale / Transduction du signal / Récepteur de facteur de croissance granulocyte-macrophage / Microglie / Galectine -3 / Souris Limites: Animals Langue: En Journal: Elife Année: 2020 Type de document: Article Pays d'affiliation: États-Unis d'Amérique Pays de publication: Royaume-Uni

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Encéphale / Transduction du signal / Récepteur de facteur de croissance granulocyte-macrophage / Microglie / Galectine -3 / Souris Limites: Animals Langue: En Journal: Elife Année: 2020 Type de document: Article Pays d'affiliation: États-Unis d'Amérique Pays de publication: Royaume-Uni