Tyrosine phosphorylation of p190 RhoGAP by Fyn regulates oligodendrocyte differentiation Meeting Abstract


Authors: Wolf, R. M.; Wilkes, J. J.; Wagner, J. A.; Chao, M. V.; Resh, M. D.
Abstract Title: Tyrosine phosphorylation of p190 RhoGAP by Fyn regulates oligodendrocyte differentiation
Meeting Title: 31st Annual Meeting of the Society for Neuroscience
Abstract: During development of the central nervous system, oligodendrocyte progenitor cells differentiate into mature myelinating cells. The molecular signals that promote this process however, are not well defined. One molecule that has been implicated in oligodendrocyte differentiation is the Src family kinase Fyn. In order to probe the function of Fyn in this system, a yeast two hybrid screen was performed. Using Fyn as bait, p190 RhoGAP was isolated in the screen of an oligodendrocyte cDNA library. Coimmunoprecipitation and in vitro binding assays verified that p190 RhoGAP bound to the Fyn SH2 domain. Phosphorylation of p190 required active Fyn tyrosine kinase and was increased three-fold upon differentiation of primary oligodendrocytes. Moreover, complex formation between p190 and p120 RasGAP occurred in differentiated oligodendrocytes, p190 RhoGAP activity is known to regulate the RhoGDP:RhoGTP ratio. Indeed, expression of dominant negative Rho in primary oligodendrocytes caused a hyperextension of processes. Conversely, constitutively activated Rho caused reduced process formation. These findings define a pathway in which Fyn activity regulates the phosphorylation of p190, leading to an increase in RhoGAP activity with a subsequent increase in RhoGDP. The increase in Rho GDP in turn regulates the morphological changes that accompany oligodendrocyte differentiation.
Keywords: meeting abstract; rhogdp:rhogtp ratio
Journal Title: Society for Neuroscience Abstracts
Volume: 27
Issue: 2
Meeting Dates: 2001 Nov 10-15
Meeting Location: San Diego, CA
ISSN: 0190-5295
Publisher: Society for Neuroscience  
Date Published: 2001-01-01
Start Page: 2379
Language: English
ACCESSION: BCI:BCI200200003925
PROVIDER: biosis
Notes: Meeting Abstract: 898.3 -- Source: Biosis