| Literature DB >> 23818270 |
Camille Nicoleau1, Christine Varela, Caroline Bonnefond, Yves Maury, Aurore Bugi, Laetitia Aubry, Pedro Viegas, Fany Bourgois-Rocha, Marc Peschanski, Anselme L Perrier.
Abstract
Wnt-ligands are among key morphogens that mediate patterning of the anterior territories of the developing brain in mammals. We qualified the role of Wnt-signals in regional specification and subregional organization of the human telencephalon using human pluripotent stem cells (hPSCs). One step neural conversion of hPSCs using SMAD inhibitors leads to progenitors with a default rostral identity. It provides an ideal biological substrate for investigating the role of Wnt signaling in both anteroposterior and dorso-ventral processes. Challenging hPSC-neural derivatives with Wnt-antagonists, alone or combined with sonic hedgehog (Shh), we found that Wnt-inhibition promote both telencephalic specification and ventral patterning of telencephalic neural precursors in a dose-dependent manner. Using optimal Wnt-antagonist and Shh-agonist signals we produced human ventral-telencephalic precursors, committed to differentiation into striatal projection neurons both in vitro and in vivo after homotypic transplantation in quinolinate-lesioned rats. This study indicates that sequentially organized Wnt-signals play a key role in the development of human ventral telencephalic territories from which the striatum arise. In addition, the optimized production of hPSC-derived striatal cells described here offers a relevant biological resource for exploring and curing Huntington disease. © AlphaMed Press.Entities:
Keywords: Cell therapy; Developmental biology; Forebrain specification; Huntington disease; Neural differentiation; Pluripotent stem cells; Striatum
Mesh:
Substances:
Year: 2013 PMID: 23818270 DOI: 10.1002/stem.1462
Source DB: PubMed Journal: Stem Cells ISSN: 1066-5099 Impact factor: 6.277