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Neural stem cell differentiation is mediated by integrin beta4 in vitro.
- Source :
-
The international journal of biochemistry & cell biology [Int J Biochem Cell Biol] 2009 Apr; Vol. 41 (4), pp. 916-24. Date of Electronic Publication: 2008 Sep 12. - Publication Year :
- 2009
-
Abstract
- Neural stem cells are capable of differentiating into three major neural cell types, but the underlying molecular mechanisms remain unclear. Here, we investigated the mechanism by which integrin beta4 modulates mouse neural stem cell differentiation in vitro. Inhibition of endogenous integrin beta4 by RNA interference inhibited the cell differentiation and the expression of fibroblast growth factor receptor 2 but not fibroblast growth factor receptor 1 or fibroblast growth factor receptor 3. Overexpression of integrin beta4 in neural stem cells promoted neural stem cell differentiation. Furthermore, integrin beta4-induced differentiation of neural stem cells was attenuated by SU5402, the inhibitor of fibroblast growth factor receptors. Finally, we investigated the role of integrin beta4 in neural stem cell survival: knockdown of integrin beta4 did not affect survival or apoptosis of neural stem cells. These data provide evidence that integrin beta4 promotes differentiation of mouse neural stem cells in vitro possibly through fibroblast growth factor receptor 2.
- Subjects :
- Animals
Cell Culture Techniques
Female
Fluorescent Antibody Technique
Gene Expression
Integrin beta4 genetics
Integrin beta4 metabolism
Mice
RNA Interference
RNA, Small Interfering genetics
Receptors, Fibroblast Growth Factor genetics
Receptors, Fibroblast Growth Factor metabolism
Transfection
Cell Differentiation physiology
Integrin beta4 physiology
Neurons cytology
Stem Cells cytology
Subjects
Details
- Language :
- English
- ISSN :
- 1878-5875
- Volume :
- 41
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- The international journal of biochemistry & cell biology
- Publication Type :
- Academic Journal
- Accession number :
- 18834954
- Full Text :
- https://doi.org/10.1016/j.biocel.2008.09.001