Open AccessBeneficial compaction of spinal cord lesion by migrating astrocytes through glycogen synthase kinase‐3 inhibition
Author(s) -
RenaultMihara Francois,
Katoh Hiroyuki,
Ikegami Takeshi,
Iwanami Akio,
Mukaino Masahiko,
Yasuda Akimasa,
Nori Satoshi,
Mabuchi Yo,
Tada Hirobumi,
Shibata Shinsuke,
Saito Ken,
Matsushita Masayuki,
Kaibuchi Kozo,
Okada Seiji,
Toyama Yoshiaki,
Nakamura Masaya,
Okano Hideyuki
Publication year - 2011
Publication title -
embo molecular medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.923
H-Index - 107
eISSN - 1757-4684
pISSN - 1757-4676
DOI - 10.1002/emmm.201100179
Subject(s) - astrocyte , gsk 3 , gsk3b , glycogen synthase , spinal cord injury , glial scar , stimulation , spinal cord , microbiology and biotechnology , chemistry , inflammation , central nervous system , pharmacology , biology , neuroscience , kinase , phosphorylation , immunology
The migratory response of astrocytes is essential for restricting inflammation and preserving tissue function after spinal cord injury (SCI), but the mechanisms involved are poorly understood. Here, we observed stimulation of in vitro astrocyte migration by the new potent glycogen synthase kinase‐3 (GSK‐3) inhibitor Ro3303544 and investigated the effect of Ro3303544 administration for 5 days following SCI in mice. This treatment resulted in accelerated migration of reactive astrocytes to sequester inflammatory cells that spared myelinated fibres and significantly promoted functional recovery. Moreover, the decreased extent of chondroitin sulphate proteoglycans and collagen IV demonstrated that scarring was reduced in Ro3303544‐treated mice. A variety of in vitro and in vivo experiments further suggested that GSK‐3 inhibition stimulated astrocyte migration by decreasing adhesive activity via reduced surface expression of β1‐integrin. Our results reveal a novel benefit of GSK‐3 inhibition for SCI and suggest that the stimulation of astrocyte migration is a feasible therapeutic strategy for traumatic injury in the central nervous system.