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In Vitro Recapitulation of Developmental Transitions in Human Neural Stem Cells.

Authors :
Ostermann L
Ladewig J
Müller FJ
Kesavan J
Tailor J
Smith A
Brüstle O
Koch P
Source :
Stem cells (Dayton, Ohio) [Stem Cells] 2019 Nov; Vol. 37 (11), pp. 1429-1440. Date of Electronic Publication: 2019 Aug 24.
Publication Year :
2019

Abstract

During nervous system development, early neuroepithelial stem (NES) cells with a highly polarized morphology and responsiveness to regionalizing morphogens give rise to radial glia (RG) cells, which generate region-specific neurons. Recently, stable neural cell populations reminiscent of NES cells have been obtained from pluripotent stem cells and the fetal human hindbrain. Here, we explore whether these cell populations, similar to their in vivo counterparts, can give rise to neural stem (NS) cells with RG-like properties and whether region-specific NS cells can be generated from NES cells with different regional identities. In vivo RG cells are thought to form from NES cells with the onset of neurogenesis. Therefore, we cultured NES cells temporarily in differentiating conditions. Upon reinitiation of growth factor treatment, cells were found to enter a developmental stage reflecting major characteristics of RG-like NS cells. These NES cell-derived NS cells exhibited a very similar morphology and marker expression as primary NS cells generated from human fetal tissue, indicating that conversion of NES cells into NS cells recapitulates the developmental progression of early NES cells into RG cells observed in vivo. Importantly, NS cells generated from NES cells with different regional identities exhibited stable region-specific transcription factor expression and generated neurons appropriate for their positional identity. Stem Cells 2019;37:1429-1440.<br /> (©AlphaMed Press 2019.)

Details

Language :
English
ISSN :
1549-4918
Volume :
37
Issue :
11
Database :
MEDLINE
Journal :
Stem cells (Dayton, Ohio)
Publication Type :
Academic Journal
Accession number :
31339593
Full Text :
https://doi.org/10.1002/stem.3065