Biological function of PDGF-induced PI-3 kinase activity: Its role in αPDGF receptor-mediated mitogenic signaling

Jin Chen Yu, J. Silvio Gutkind, Daruka Mahadevan, Weiqun Li, Kimberly A. Meyers, Jacalyn H. Pierce, Mohammad A. Heidaran

Producción científica: Articlerevisión exhaustiva

36 Citas (Scopus)


The tyrosine phosphorylation sites in the human αPDGF receptor (αPDGFR) required for association with PI-3 kinase have been identified as tyrosines 731 and 742. Mutation of either tyrosine substantially reduced PDGF-induced PI-3 kinase activity but did not impair the receptor-mediated mitogenic response. We sought to determine whether PDGF-induced PI-3 kinase activity could be further ablated so as to exclude a low threshold requirement for PDGFR signal transduction. Thus, we mutated both tyrosine 731 and 742 and expressed the double mutant (Y731F/Y742F) in 32D hematopoietic cells. In such transfectants, PDGF induced no detectable receptor-associated or anti-P-Tyr recoverable PI-3 kinase activity. Under the same conditions, neither mobility shift of raf-1 nor tyrosine phosphorylation of either PLCγ or MAP kinase was impaired. 32D transfectants expressing the double mutant showed wild-type αPDGFR levels of mitogenic and chemotactic responses to PDGF. To examine the effect of the double mutation in cells that normally respond to PDGF, we generated chimeras in which the cytoplasmic domains of wild-type αPDGFR, Y731F, and Y731F/Y742F were linked to the extracellular domain of colony- stimulating factor-1 (CSF-1) receptor (fms). After introduction of the chimeric receptors into mouse NIH/3T3 fibroblasts, the ability of CSF-1 to stimulate growth of these transfectants was examined. Our data show that all these chimeric receptors exhibited similar abilities to mediate CSF-1- stimulated cell growth. These findings lead us to conclude that PDGF-induced PI-3 kinase activity is not required for PDGF-stimulated mitogenic pathway in both NIH/3T3 fibroblasts and 32D hematopoietic cells.

Idioma originalEnglish (US)
Páginas (desde-hasta)479-487
Número de páginas9
PublicaciónJournal of Cell Biology
EstadoPublished - oct 1994
Publicado de forma externa

ASJC Scopus subject areas

  • Cell Biology


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