Coupled proliferation and apoptosis maintain the rapid turnover of microglia in the adult brain
| Autor: | Askew, K, Li, K, Olmos-Alonso, A, Garcia-Moreno, F, Liang, Y, Richardson, P, Tipton, T, Chapman, MA, Riecken, K, Beccari, S, Sierra, A, Molnár, Z, Cragg, MS, Garaschuk, O, Perry, VH, Gomez-Nicola, D |
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| Jazyk: | angličtina |
| Rok vydání: | 2017 |
| Předmět: | |
| Zdroj: | Cell Reports, Vol 18, Iss 2, Pp 391-405 (2017) Cell Reports |
| Popis: | Summary Microglia play key roles in brain development, homeostasis, and function, and it is widely assumed that the adult population is long lived and maintained by self-renewal. However, the precise temporal and spatial dynamics of the microglial population are unknown. We show in mice and humans that the turnover of microglia is remarkably fast, allowing the whole population to be renewed several times during a lifetime. The number of microglial cells remains steady from late postnatal stages until aging and is maintained by the spatial and temporal coupling of proliferation and apoptosis, as shown by pulse-chase studies, chronic in vivo imaging of microglia, and the use of mouse models of dysregulated apoptosis. Our results reveal that the microglial population is constantly and rapidly remodeled, expanding our understanding of its role in the maintenance of brain homeostasis. Graphical Abstract Highlights • The microglial population is formed without the perinatal infiltration of monocytes • The microglial density remains remarkably stable over a mouse or human lifetime • In the mouse and human brain, microglia turn over several times during a lifetime • Microglia self-renewal is maintained by coupled proliferation and apoptosis The mechanism or mechanisms underlying microglial homeostasis are unknown. Askew et al. show that microglia self-renewal is maintained by coupled proliferation and apoptosis, resulting in a stable microglia number over a mouse or human lifetime. |
| Databáze: | OpenAIRE |
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