The dissociation and degradation of internalized insulin occur in the endosomes of rat hepatoma cells

Jonathan M. Backer, C. Ronald Kahn, Morris F. White

Research output: Contribution to journalArticle

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Abstract

We have studied the intracellular processing of insulin in the rat hepatoma cell line Fao. Fao cells internalized cohorts of surface-bound 125I-insulin or 125I-insulin-like growth factor II within 3-5 min. Degraded 125I-insulin-like growth factor II did not appear in the medium until 20-30 min after uptake, consistent with a time course of lysosomal delivery. In contrast, internalized insulin was completely degraded within 7-10 min. The half-times for dissociation and degradation of internalized insulin were identical at 37°C (3 min), suggesting that the two processes occurred in the same compartment. Subcellular fractionation of Fao cells showed that a pulse of internalized insulin was largely intact after 3 min and associated with a light membrane fraction devoid of lysosomal markers. After an additional 4 min, the amount of insulin in this compartment decreased by 40%, with an increase in degraded insulin in the cytosol; no transfer of intact insulin to lysosomes or the cytosol was detected. The relationship between insulin-receptor dissociation and insulin degradation was further studied with inhibitors of insulin processing. Monensin blocked both dissociation and degradation of internalized insulin, as did incubation of the cells at 20°C, suggesting that both endosomal acidification and endosomal fusion were required for insulin processing. At 25°C, dissociation (+t1/2 = 12.9 min) preceded degradation (+t1/2 = 15.8 min). Inhibitors of lysosomal proteases were without effect on the half-time for either process. In contrast, bacitracin, an inhibitor of insulin degradation, caused a 2-fold increase in the half-times for both dissociation and degradation. Thus, intracellular insulin dissociation and degradation are tightly coupled endosomal processes in Fao cells, and insulin degradation facilitates the dissociation of insulin from its receptor inside the cell.

Original languageEnglish (US)
Pages (from-to)14828-14835
Number of pages8
JournalJournal of Biological Chemistry
Volume265
Issue number25
StatePublished - Sep 5 1990
Externally publishedYes

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Endosomes
Rats
Hepatocellular Carcinoma
Insulin
Degradation
Corrosion inhibitors
Insulin-Like Growth Factor II
Insulin Receptor
Cytosol
Processing
Cells
Bacitracin
Cell Fractionation
Monensin
Acidification
Fractionation
Lysosomes
Protease Inhibitors

ASJC Scopus subject areas

  • Biochemistry

Cite this

The dissociation and degradation of internalized insulin occur in the endosomes of rat hepatoma cells. / Backer, Jonathan M.; Kahn, C. Ronald; White, Morris F.

In: Journal of Biological Chemistry, Vol. 265, No. 25, 05.09.1990, p. 14828-14835.

Research output: Contribution to journalArticle

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