Chronic ethanol administration impairs receptor‐mediated endocytosis of epidermal growth factor by rat hepatocytes

Douglas D. Dalke, Michael Floyd Sorrell, Carol A Casey, Dean J. Tuma

Research output: Contribution to journalArticle

53 Scopus citations


The effects of chronic ethanol administration on the receptor‐mediated endocytosis of epidermal growth factor were studied in isolated rat hepatocytes. In initial experiments, it was demonstrated that significantly less ligand was bound by hepatocytes isolated from rats fed an ethanol liquid diet for 5 to 7 wk than by cells isolated from chow‐fed or pair‐fed controls. Reduced binding was shown to be primarily caused by a decreased number of surface receptors rather than by changes in receptor affinity. When hepatocytes were incubated at 37° C in the presence of a large saturating concentration of epidermal growth factor (80 nmol/L), intracellular levels of the ligand were significantly lower in cells from the ethanol‐fed animals. However, no effect on degradation of the ligand was observed under those conditions. A defect in the initial stages of receptor‐ligand internalization was also indicated because less surface‐bound ligand was internalized and subsequently degraded in cells from the ethanoltreated rats. When the endocytosis of a lower, more physiological concentration of the growth factor (0.5 nmol/L) was studied, both the uptake of ligand and its degradation were markedly impaired in hepatocytes from the ethanol‐fed animals. These results indicate that chronic ethanol administration impairs the receptor‐mediated endocytosis of epidermal growth factor by the liver. The major impairment appears to be a reduction of cell surface receptors; however, other steps of the endocytotic pathway also appear to be affected. These altered steps include defective receptor‐ligand internalization and changes in intracellular processing of the ligand leading to decreased degradation. (HEPATOLOGY 1990;12:1085–1091).

Original languageEnglish (US)
Pages (from-to)1085-1091
Number of pages7
Issue number5
Publication statusPublished - Nov 1990


ASJC Scopus subject areas

  • Hepatology

Cite this