Fate Mapping Analysis Reveals That Adult Microglia Derive from Primitive Macrophages

Florent Ginhoux(Singapore Immunology Network), Melanie Greter(Icahn School of Medicine at Mount Sinai), Marylène Leboeuf(Icahn School of Medicine at Mount Sinai), Sayan Nandi(Albert Einstein College of Medicine), Peter See(Singapore Immunology Network), Şölen Gökhan(Albert Einstein College of Medicine), Mark F. Mehler(Albert Einstein College of Medicine), Simon J. Conway(Indiana University – Purdue University Indianapolis), Lai Guan Ng(Singapore Immunology Network), E. Richard Stanley(Albert Einstein College of Medicine), Igor M. Samokhvalov(Kobe Steel (Japan)), Miriam Mérad(Icahn School of Medicine at Mount Sinai)
Science
October 21, 2010
Cited by 5,067Open Access
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Abstract

Microglia are the resident macrophages of the central nervous system and are associated with the pathogenesis of many neurodegenerative and brain inflammatory diseases; however, the origin of adult microglia remains controversial. We show that postnatal hematopoietic progenitors do not significantly contribute to microglia homeostasis in the adult brain. In contrast to many macrophage populations, we show that microglia develop in mice that lack colony stimulating factor-1 (CSF-1) but are absent in CSF-1 receptor-deficient mice. In vivo lineage tracing studies established that adult microglia derive from primitive myeloid progenitors that arise before embryonic day 8. These results identify microglia as an ontogenically distinct population in the mononuclear phagocyte system and have implications for the use of embryonically derived microglial progenitors for the treatment of various brain disorders.


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