Stage-specific roles of FGF2 signaling in human neural development

Investor logo

Warning

This publication doesn't include Faculty of Arts. It includes Faculty of Medicine. Official publication website can be found on muni.cz.
Authors

GRABIEC Marta HŘÍBKOVÁ Hana VAŘECHA Miroslav STŘÍTECKÁ Dana HAMPL Aleš DVOŘÁK Petr SUN Yuh-Man

Year of publication 2016
Type Article in Periodical
Magazine / Source Stem Cell Research
MU Faculty or unit

Faculty of Medicine

Citation
Doi http://dx.doi.org/10.1016/j.scr.2016.08.012
Field Genetics and molecular biology
Keywords Neural developmental modeling; Embryonic stem cells; Neural fate; Neurogenesis; FGF2 signaling; Neural stem cell niche
Description This study elucidated the stage-specific roles of FGF2 signaling during neural development using in-vitro human embryonic stem cell-based developmental modeling. We found that the dysregulation of FGF2 signaling prior to the onset of neural induction resulted in the malformation of neural rosettes (a neural tube-like structure), despite cells having undergone neural induction. The aberrant neural rosette formation may be attributed to the misplacement of ZO-1, which is a polarized tight junction protein and shown co-localized with FGF2/FGFR1 in the apical region of neural rosettes, subsequently led to abnormal neurogenesis. Moreover, the FGF2 signaling inhibition at the stage of neural rosettes caused a reduction in cell proliferation, an increase in numbers of cells with cell-cycle exit, and premature neurogenesis. These effects may be mediated by NUMB, to which expression was observed enriched in the apical region of neural rosettes after FGF2 signaling inhibition coinciding with the disappearance of PAX6+/Ki67+ neural stem cells and the emergence of MAP2+ neurons. Moreover, our results suggested that the hESC-based developmental system reserved a similar neural stem cell niche in vivo.
Related projects:

You are running an old browser version. We recommend updating your browser to its latest version.