Rapgef2, a guanine nucleotide exchange factor for Rap1 small GTPases, plays a crucial role in adherence junction (AJ) formation in radial glial cells through ERK-mediated upregulation of the AJ-constituent protein expression
Autor: | Tohru Kataoka, Maged Ibrahim Farag, Yoko Yoshikawa, Kazuhiro Maeta |
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Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
MAPK/ERK pathway MAP Kinase Signaling System Ependymoglial Cells Biophysics GTPase Biology Biochemistry Mice 03 medical and health sciences Downregulation and upregulation Conditional gene knockout Animals Guanine Nucleotide Exchange Factors Extracellular Signal-Regulated MAP Kinases Molecular Biology Cells Cultured Mice Knockout Kinase RAPGEF2 Adherens Junctions Cell Biology Molecular biology Up-Regulation Cell biology 030104 developmental biology Rap1 sense organs Guanine nucleotide exchange factor |
Zdroj: | Biochemical and Biophysical Research Communications. 493:139-145 |
ISSN: | 0006-291X |
DOI: | 10.1016/j.bbrc.2017.09.062 |
Popis: | Rapgef2 and Rapgef6 define a subfamily of guanine nucleotide exchange factors for Rap1, characterized by possession of the Ras/Rap-associating domains and implicated in the etiology of schizophrenia. We previously found that dorsal telencephalon-specific Rapgef2 conditional knockout mice exhibits severe defects in formation of apical surface adherence junctions (AJs) and localization of radial glial cells (RGCs). In this study, we analyze the underlying molecular mechanism by using primary cultures of RGCs established from the developing cerebral cortex. The results show that Rapgef2-deficient RGCs exhibit a decreased ability of neurosphere formation, morphological changes represented by regression of radial glial (RG) fibers and reduced expression of AJ-constituent proteins such as N-cadherin, zonula occludens-1, E-cadherin and β-catenin. Moreover, siRNA-mediated knockdown of Rapgef2 or Rap1A inhibits the AJ protein expression and RG fiber formation while overexpression of Rapgef2, Rapgef6, Rap1AG12V or Rap1BG12V in Rapgef2-deficient RGCs restores them. Furthermore, Rapgef2-deficient RGCs exhibit a reduction in phosphorylation of extracellular signal-regulated kinase (ERK) leading to downregulation of the expression of c-jun, which is implicated in the AJ protein expression. These results indicate a crucial role of the Rapgef2-Rap1A-ERK-c-jun pathway in regulation of the AJ formation in RGCs. |
Databáze: | OpenAIRE |
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