Affiliation:
1. Cell Biology Laboratory and Department of Medicine, Mount Zion Hospital and Medical Center; and the Departments of Physiology and Medicine, University of California San Francisco, San Francisco, California
Abstract
The influence of insulin on the downregulation of its receptor was studied in AR42J cultured pancreatic acinar cells, a cell line that has been demonstrated to be metabolically responsive to insulin. Downregulation induced by insulin was time and dose dependent. After a 20-h incubation with 1 μM insulin, Scatchard analysis revealed ∼80% loss of insulin receptors. Studies of receptor half-life indicated that treatment with insulin accelerated the degradation of both the α and β-subunits of the insulin receptor by 30–60%. In addition, biosynthetic-labeling studies indicated that insulin inhibited the biosynthesis of the insulin-receptor precursor by >30%. This decreased biosynthesis of the precursor was associated with decreased production of mature receptor subunits. Poly(A)+ RNA was extracted from control cells and cells treated for 24 hwith 100 nM insulin. Slot blots and Northern transfers revealed that insulin induced an ∼ 50% decrease in insulin-receptor mRNA levels. Therefore, these studies indicate that insulin may diminish the concentration of its receptors in target cells by at least two mechanisms: acceleration of receptor degradation and inhibition of receptor biosynthesis at the level of mRNA.
Publisher
American Diabetes Association
Subject
Endocrinology, Diabetes and Metabolism,Internal Medicine
Cited by
47 articles.
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