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Lange Canhos, L. ; Chen, M.* ; Falk, S. ; Popper, B.* ; Straub, T.* ; Götz, M. ; Sirko, S.

Repetitive injury and absence of monocytes promote astrocyte self-renewal and neurological recovery.

Glia 69, 165-181 (2021)
Postprint DOI PMC
Open Access Hybrid
Creative Commons Lizenzvertrag
Unlike microglia and NG2 glia, astrocytes are incapable of migrating to sites of injury in the posttraumatic cerebral cortex, instead relying on proliferation to replenish their numbers and distribution in the affected region. However, neither the spectrum of their proliferative repertoire nor their postinjury distribution has been examined in vivo. Using a combination of different thymidine analogs and clonal analysis in a model of repetitive traumatic brain injury, we show for the first time that astrocytes that are quiescent following an initial injury can be coerced to proliferate after a repeated insult in the cerebral cortex grey matter. Interestingly, this process is promoted by invasion of monocytes to the injury site, as their genetic ablation (using CCR2(-/-)mice) increased the number of repetitively dividing astrocytes at the expense of newly proliferating astrocytes in repeatedly injured parenchyma. These differences profoundly affected both the distribution of astrocytes and recovery period for posttraumatic behavior deficits suggesting key roles of astrocyte self-renewal in brain repair after injury.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Astrocyte Topology ; Cognitive Disfunction ; Inflammation ; Reactive Gliosis ; Self-renew ; Tbi; Experimental Autoimmune Encephalomyelitis; Traumatic Brain-injury; Focal Laser-lesions; Extracellular-matrix; Reactive Astrocytes; Cerebral-cortex; Neural Stem; Cortical Plasticity; Clonal Expansion; Cells
Sprache englisch
Veröffentlichungsjahr 2021
Prepublished im Jahr 2020
HGF-Berichtsjahr 2020
ISSN (print) / ISBN 0894-1491
e-ISSN 1098-1136
Zeitschrift Glia
Quellenangaben Band: 69, Heft: 1, Seiten: 165-181 Artikelnummer: , Supplement: ,
Verlag Wiley
Verlagsort 111 River St, Hoboken 07030-5774, Nj Usa
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Stem Cell Research (ISF)
POF Topic(s) 30204 - Cell Programming and Repair
Forschungsfeld(er) Stem Cell and Neuroscience
PSP-Element(e) G-500800-001
DOI 10.1002/glia.23893
WOS ID WOS:000563864400001
Scopus ID 85088862790
PubMed ID 32744730
Erfassungsdatum 2020-09-23
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