Description:
<jats:title>Abstract</jats:title><jats:p>Stroke is the leading cause of adult disability. Endogenous neural stem/progenitor cells (NSPCs) originating from the subventricular zone (SVZ) contribute to the brain repair process. However, molecular mechanisms underlying CNS disease-induced SVZ NSPC-redirected migration to the lesion area are poorly understood. Here, we show that genetic depletion of the p75 neurotrophin receptor (<jats:italic>p75</jats:italic><jats:sup><jats:italic>NTR−/−</jats:italic></jats:sup>) in mice reduced SVZ NSPC migration towards the lesion area after cortical injury and that <jats:italic>p75</jats:italic><jats:sup><jats:italic>NTR−/−</jats:italic></jats:sup> NSPCs failed to migrate upon BDNF stimulation in vitro. Cortical injury rapidly increased p75<jats:sup>NTR</jats:sup> abundance in SVZ NSPCs via bone morphogenetic protein (BMP) receptor signaling. SVZ-derived <jats:italic>p75</jats:italic><jats:sup><jats:italic>NTR−/−</jats:italic></jats:sup> NSPCs revealed an altered cytoskeletal network- and small GTPase family-related gene and protein expression. In accordance, BMP-treated non-migrating <jats:italic>p75</jats:italic><jats:sup><jats:italic>NTR−/−</jats:italic></jats:sup> NSPCs revealed an altered morphology and α-tubulin expression compared to BMP-treated migrating wild-type NSPCs. We propose that BMP-induced p75<jats:sup>NTR</jats:sup> abundance in NSPCs is a regulator of SVZ NSPC migration to the lesion area via regulation of the cytoskeleton following cortical injury.</jats:p>