Cellular gangliosides promote growth factor-induced proliferation of fibroblasts

Cell surface gangliosides have been proposed as modulators of transmembrane signaling. In this study, we used two complementary approaches to investig ate the function of cellular gangliosides in the response of mammalian fibr oblasts to growth factors. First, inhibition of glucosyl ceramide synthase by a new specific inhibitor of D-1-threo-1-phenyl-2-hexadecanoylamino-3-pyr rolidino-1-propanol-HCl (glucosylceramide synthase), which depletes cellula r gangliosides at a concentration of 1 muM without causing an increase in c eramide levels, blocked epidermal growth factor-stimulated proliferation of fibroblasts. Similarly, responses to several other growth factors that act ivate receptor tyrosine kinases, including fibroblast growth factor, insuli n-like growth factor-I, and platelet-derived growth factor, were inhibited by 50-100%. Conversely, enrichment of cellular gangliosides by preincubatio n of the mouse and human fibroblasts with exogenously added gangliosides en hanced growth factor-elicited cell proliferation. Novel findings of this st udy, distinguishing it from previous similar studies, include differential effects of preincubation versus continuous incubation of cells with ganglio sides on growth factor-dependent cell proliferation and the growth factor-l ike action of NeuNAc alpha2-3Gal beta1-3GalNAc beta1-4(NeuNAc alpha2-3)Gal beta1-4Glc beta1-1Cer when cells are pretreated with the ganglioside.