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.
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Original Articles|
February 01 1989
Mechanisms of Insulin-Induced Insulin-Receptor Downregulation: Decrease of Receptor Biosynthesis and mRNA Levels
Yoshinori Okabayashi;
Yoshinori Okabayashi
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
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Betty A Maddux;
Betty A Maddux
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
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Alexander R McDonald;
Alexander R McDonald
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
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Craig D Logsdon;
Craig D Logsdon
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
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John A Williams;
John A Williams
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
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Ira D Goldfine
Ira D Goldfine
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
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Address correspondence and reprint requests to Ira D. Goldfine, MD, Cell Biology Laboratory, Mount Zion Hospital and Medical Center, P.O. Box 7921, San Francisco, CA 94120.
Diabetes 1989;38(2):182–187
Article history
Received:
November 18 1987
Revision Received:
August 30 1988
Accepted:
August 30 1988
PubMed:
2644141
Citation
Yoshinori Okabayashi, Betty A Maddux, Alexander R McDonald, Craig D Logsdon, John A Williams, Ira D Goldfine; Mechanisms of Insulin-Induced Insulin-Receptor Downregulation: Decrease of Receptor Biosynthesis and mRNA Levels. Diabetes 1 February 1989; 38 (2): 182–187. https://doi.org/10.2337/diab.38.2.182
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