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. 1990 May;26(5):537-42.
doi: 10.1007/BF02624098.

Density-induced down regulation of epidermal growth factor receptors

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Density-induced down regulation of epidermal growth factor receptors

A Rizzino et al. In Vitro Cell Dev Biol. 1990 May.

Abstract

Previous studies have shown that cell density can regulate the binding of several growth factors. To determine whether cell density exerts a uniform effect on the expression of epidermal growth factor (EGF) receptors, seven cell lines were examined in detail. For each cell line, EGF binding was found to decrease as cell density increases. Scatchard analysis of the binding data reveals that decreases in EGF binding are due to reductions in the number of cell surface EGF receptors. The only apparent exception is the effect of cell density on the binding of EGF to A-431 cells. For these cells, increases in cell density lead to two effects: decreases in the number of high affinity EGF receptors and increases in the total number of EGF receptors. In addition to the effects of cell density on EGF receptors, it was determined that increases in cell density can coordinately down-regulate receptors for as many as four different growth factors. Overall, the findings described in this report for EGF and those previously described for transforming growth factor type-beta (TGF-beta) and fibroblast growth factor (FGF) demonstrate the existence of a common mechanism for down-regulating growth factor receptors.

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References

    1. Biochem Pharmacol. 1989 Jul 1;38(13):2053-60 - PubMed
    1. Science. 1978 Oct 20;202(4365):313-5 - PubMed
    1. Proc Natl Acad Sci U S A. 1977 Nov;74(11):5046-50 - PubMed
    1. EMBO J. 1984 May;3(5):929-37 - PubMed
    1. J Cell Biol. 1982 Apr;93(1):1-4 - PubMed

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