| Literature DB >> 29727663 |
Prajay T Shah1, Jo A Stratton2, Morgan Gail Stykel3, Sepideh Abbasi3, Sandeep Sharma1, Kyle A Mayr1, Kathrin Koblinger1, Patrick J Whelan1, Jeff Biernaskie4.
Abstract
Ependymal cells are multi-ciliated cells that form the brain's ventricular epithelium and a niche for neural stem cells (NSCs) in the ventricular-subventricular zone (V-SVZ). In addition, ependymal cells are suggested to be latent NSCs with a capacity to acquire neurogenic function. This remains highly controversial due to a lack of prospective in vivo labeling techniques that can effectively distinguish ependymal cells from neighboring V-SVZ NSCs. We describe a transgenic system that allows for targeted labeling of ependymal cells within the V-SVZ. Single-cell RNA-seq revealed that ependymal cells are enriched for cilia-related genes and share several stem-cell-associated genes with neural stem or progenitors. Under in vivo and in vitro neural-stem- or progenitor-stimulating environments, ependymal cells failed to demonstrate any suggestion of latent neural-stem-cell function. These findings suggest remarkable stability of ependymal cell function and provide fundamental insights into the molecular signature of the V-SVZ niche.Entities:
Keywords: V-SVZ; VEGF; ependymal cell; neural stem cell; neurogenesis; single cell RNA-seq; stroke; transcriptomics
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Year: 2018 PMID: 29727663 DOI: 10.1016/j.cell.2018.03.063
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582