| Literature DB >> 29276142 |
Hideo Jinnou1, Masato Sawada2, Koya Kawase1, Naoko Kaneko2, Vicente Herranz-Pérez3, Takuya Miyamoto2, Takumi Kawaue4, Takaki Miyata4, Yasuhiko Tabata5, Toshihiro Akaike6, José Manuel García-Verdugo7, Itsuki Ajioka8, Shinji Saitoh9, Kazunobu Sawamoto10.
Abstract
Radial glia (RG) are embryonic neural stem cells (NSCs) that produce neuroblasts and provide fibers that act as a scaffold for neuroblast migration during embryonic development. Although they normally disappear soon after birth, here we found that RG fibers can persist in injured neonatal mouse brains and act as a scaffold for postnatal ventricular-subventricular zone (V-SVZ)-derived neuroblasts that migrate to the lesion site. This injury-induced maintenance of RG fibers has a limited time window during post-natal development and promotes directional saltatory movement of neuroblasts via N-cadherin-mediated cell-cell contacts that promote RhoA activation. Transplanting an N-cadherin-containing scaffold into injured neonatal brains likewise promotes migration and maturation of V-SVZ-derived neuroblasts, leading to functional improvements in impaired gait behaviors. Together these results suggest that RG fibers enable postnatal V-SVZ-derived neuroblasts to migrate toward sites of injury, thereby enhancing neuronal regeneration and functional recovery from neonatal brain injuries.Entities:
Keywords: N-cadherin; gait behavior; neonatal brain injury; neuronal migration; neuronal regeneration; postnatal neurogenesis; radial glial cell; ventricular-subventricular zone
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Year: 2017 PMID: 29276142 DOI: 10.1016/j.stem.2017.11.005
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633