Fiche publication
Date publication
mai 2017
Journal
Cell reports
Auteurs
Membres identifiés du Cancéropôle Est :
Dr GACHET Christian
Tous les auteurs :
Shinozaki Y, Shibata K, Yoshida K, Shigetomi E, Gachet C, Ikenaka K, Tanaka KF, Koizumi S
Lien Pubmed
Résumé
Microglia and astrocytes become reactive following traumatic brain injury (TBI). However, the coordination of this reactivity and its relation to pathophysiology are unclear. Here, we show that microglia transform astrocytes into a neuroprotective phenotype via downregulation of the P2Y purinergic receptor. TBI initially caused microglial activation in the injury core, followed by reactive astrogliosis in the peri-injured region and formation of a neuroprotective astrocyte scar. Equivalent changes to astrocytes were observed in vitro after injury. This change in astrocyte phenotype resulted from P2Y receptor downregulation, mediated by microglia-derived cytokines. In mice, astrocyte-specific P2Y receptor overexpression (Astro-P2YOE) counteracted scar formation, while astrocyte-specific P2Y receptor knockdown (Astro-P2YKD) facilitated scar formation, suggesting critical roles of P2Y receptors in the transformation. Astro-P2YOE and Astro-P2YKD mice showed increased and reduced neuronal damage, respectively. Altogether, our findings indicate that microglia-astrocyte interaction, involving a purinergic signal, is essential for the formation of neuroprotective astrocytes.
Mots clés
Animals, Astrocytes, cytology, Brain Injuries, Traumatic, metabolism, Cell Communication, Cells, Cultured, Cytokines, metabolism, Down-Regulation, Gliosis, metabolism, Male, Mice, Mice, Inbred C57BL, Microglia, metabolism, Nerve Regeneration, Phenotype, Receptors, Purinergic P2Y1, genetics
Référence
Cell Rep. 2017 05 9;19(6):1151-1164