Effects of retinoic acid on the binding and mitogenic activity of epidermal growth factor
- PMID: 6282898
- DOI: 10.1002/jcp.1041100302
Effects of retinoic acid on the binding and mitogenic activity of epidermal growth factor
Abstract
In this study the effects of retinoic acid on the binding and mitogenic activity of epidermal growth factor (EGF) in mouse fibroblast Balb/c 3T6 cells are further examined. Retinoic acid treatment of 3T6 cells results in a sixfold enhancement of 125I-labeled mouse EGF binding when assayed at 37 degrees C. In both retinoic acid-treated and control cells, cell-associated 125I-EGF is rapidly internalized, degraded, and secreted. Retinoic acid treatment does not seem to have a significant effect on the rate of internalization and degradation of EGF. At 0 degrees C, internalization of EGF is strongly inhibited in both retinoic acid-treated and control cells. Under these conditions retinoic acid-treated cells still exhibit a tenfold higher level of EGF binding compared to control cells. When exposed to high concentrations of EGF both retinoic acid-treated and control cells "down-regulate" their EGF receptors. And although the growth rate of retinoic acid-treated cells is about half that of control cells, the rate at which EGF binding capacity is restored after down-regulation is about three times as fast as in control cells. No direct antagonism on EGF binding was observed between the tumor promoter 12-O-tetradecanoyl-phorbol-13-acetate (TPA) and retinoic acid. EGF is a potent mitogen for 3T6 cells in serum-free medium; retinoic acid inhibits the mitogenic activity of EGF even though it increases EGF binding. Retinoic acid also inhibits cell proliferation induced by sarcoma growth factor (SGF) and insulin.
Similar articles
-
Differential responsiveness of normal and simian virus 40-transformed BALB/c 3T3 cells to retinoic acid: rapid enhancement of epidermal growth factor receptor binding in a simian virus 40-3T3 variant.Cancer Res. 1987 Oct 1;47(19):4995-9. Cancer Res. 1987. PMID: 3040236
-
Tumor promoter-induced inhibition of epidermal growth factor binding to cultured mouse primary epidermal cells.Cancer Res. 1981 Jun;41(6):2308-14. Cancer Res. 1981. PMID: 6972249
-
Human papillomavirus 16 immortalization of normal human ectocervical epithelial cells alters retinoic acid regulation of cell growth and epidermal growth factor receptor expression.Cancer Res. 1993 Oct 1;53(19):4511-7. Cancer Res. 1993. PMID: 8402622
-
Modulation of the epidermal growth factor receptor by mitogenic ligands: effects of bombesin and role of protein kinase C.Cancer Surv. 1985;4(4):729-65. Cancer Surv. 1985. PMID: 3916643 Review.
-
Hormone-induced modification of EGF receptor proteolysis in the induction of EGF action.J Supramol Struct. 1979;12(4):517-31. doi: 10.1002/jss.400120411. J Supramol Struct. 1979. PMID: 233024 Review.
Cited by
-
Bradykinin-induced growth inhibition of normal rat kidney (NRK) cells is paralleled by a decrease in epidermal-growth-factor receptor expression.Biochem J. 1994 Mar 1;298 ( Pt 2)(Pt 2):335-40. doi: 10.1042/bj2980335. Biochem J. 1994. PMID: 8135739 Free PMC article.
-
Altered distribution of the nuclear receptor RAR beta accompanies proliferation and differentiation changes caused by retinoic acid in Caco-2 cells.In Vitro Cell Dev Biol Anim. 1996 Jan;32(1):53-61. doi: 10.1007/BF02722994. In Vitro Cell Dev Biol Anim. 1996. PMID: 8835319
-
The Retinol Circulating Complex Releases Hormonal Ligands During Acute Stress Disorders.Front Endocrinol (Lausanne). 2018 Sep 4;9:487. doi: 10.3389/fendo.2018.00487. eCollection 2018. Front Endocrinol (Lausanne). 2018. PMID: 30233492 Free PMC article. Review.
-
Retinoic acid enhances the proliferation of smooth muscle cells.Experientia. 1987 Feb 15;43(2):196-8. doi: 10.1007/BF01942850. Experientia. 1987. PMID: 3817104
-
Sustained release of epidermal growth factor accelerates wound repair.Proc Natl Acad Sci U S A. 1985 Nov;82(21):7340-4. doi: 10.1073/pnas.82.21.7340. Proc Natl Acad Sci U S A. 1985. PMID: 3877308 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources