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Buffo, A. ; Rite, I. ; Tripathi, P. ; Lepier, A.* ; Colak, D. ; Horn, A.P. ; Mori, T. ; Götz, M.

Origin and progeny of reactive gliosis: A source of multipotent cells in the injured brain.

Proc. Natl. Acad. Sci. U.S.A. 105, 3581-3586 (2008)
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Reactive gliosis is the universal reaction to brain injury, but the precise origin and subsequent fate of the glial cells reacting to injury are unknown. Astrocytes react to injury by hypertrophy and up-regulation of the glial-fibrillary acidic protein (GFAP). Whereas mature astrocytes do not normally divide, a subpopulation of the reactive GFAP(+) cells does so, prompting the question of whether the proliferating GFAP(+) cells arise from endogenous glial progenitors or from mature astrocytes that start to proliferate in response to brain injury. Here we show by genetic fate mapping and cell type-specific viral targeting that quiescent astrocytes start to proliferate after stab wound injury and contribute to the reactive gliosis and proliferating GFAP(+) cells. These proliferating astrocytes remain within their lineage in vivo, while a more favorable environment in vitro revealed their multipotency and capacity for self-renewal. Conversely, progenitors present in the adult mouse cerebral cortex labeled by NG2 or the receptor for the platelet-derived growth factor (PDGFRalpha) did not form neurospheres after (or before) brain injury. Taken together, the first fate-mapping analysis of astrocytes in the adult mouse cerebral cortex shows that some astrocytes acquire stem cell properties after injury and hence may provide a promising cell type to initiate repair after brain injury.
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Publication type Article: Journal article
Document type Scientific Article
Corresponding Author
Keywords astrocytes; cell fate; cerebral cortex; stem cells; NEURAL STEM-CELLS; ADULT SPINAL-CORD; GROWTH-FACTOR; IN-VIVO; LENTIVIRAL VECTOR; GENE DELIVERY; MOUSE-BRAIN; ASTROCYTES; EXPRESSION; NEURONS
ISSN (print) / ISBN 0027-8424
e-ISSN 1091-6490
Journal Proceedings of the National Academy of Sciences of the United States of America
Quellenangaben Volume: 105, Issue: 9, Pages: 3581-3586 Article Number: , Supplement: ,
Publisher National Academy of Sciences
Non-patent literature Publications
Reviewing status Peer reviewed
Institute(s) Institute of Stem Cell Research (ISF)