Abstract

The plasma membrane is not homogeneous but contains specific subcompartments characterized by their unique lipid and protein composition. Based on their enrichment in various signaling molecules, these membrane microdomains are recognized to be sites of localized signal transduction for a number of extracellular stimuli. We have previously shown that fibroblast growth factor-2 (FGF2) induced a specific signaling response within a lipid raft membrane microdomain in human neuroblastoma cells characterized by the tyrosine phosphorylation of a p80 phosphoprotein. Herein, we show that this protein is the signaling adaptor FRS2 and that it is localized exclusively to lipid rafts in vitro and in vivo. We have examined how the tyrosine phosphorylation and serine-threonine phosphorylation of FRS2 within lipid rafts affect the response of cells to FGF2 signaling. Our data suggest that activation of protein kinase C, Src family kinases, and MEK1/2 are involved in regulating serine-threonine phosphorylation of FRS2, which can indirectly affect FRS2 phosphotyrosine levels. We also show that Grb2 is recruited to lipid rafts during signaling events and that activation of MEK1/2 by different mechanisms within lipid rafts may lead to different cellular responses. This work suggests that compartmentalized signaling within lipid rafts may provide a level of specificity for growth factor signaling.

Highlights

  • Fibroblast growth factors (FGFs)1 constitute a large family of peptide hormones that influence a wide variety of biological processes such as angiogenesis, embryogenesis, differentiation, and proliferation depending on the cell type [1, 2]

  • We have examined fibroblast growth factor-2 (FGF2) signaling through FRS2 within lipid rafts and show that serine-threonine phosphorylation of FRS2 is dependent on a pathway involving protein kinase C (PKC), Src family kinases, and MEK1/2 and that FGF2 signaling through MEK1/2 may have different phenotypic consequences in the cell depending upon the pathway used for activation of MEK1/2

  • Western blotting showed that FRS2 is localized exclusively to lipid raft fractions and correlates with the FGF2-induced phosphotyrosine seen at 80 kDa in the lipid raft fraction (Fig. 1A)

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Summary

Introduction

Fibroblast growth factors (FGFs)1 constitute a large family of peptide hormones that influence a wide variety of biological processes such as angiogenesis, embryogenesis, differentiation, and proliferation depending on the cell type [1, 2]. We have previously shown that fibroblast growth factor-2 (FGF2) induced a specific signaling response within a lipid raft membrane microdomain in human neuroblastoma cells characterized by the tyrosine phosphorylation of a p80 phosphoprotein.

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