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This Article Full Text Full Text (PDF) All Versions of this Article: 294/1/E61    most recent 00358.2007v1 Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Web of Science (3) Citing Articles via Google Scholar Google Scholar Articles by Harada, N. Articles by Inagaki, N. Search for Related Content PubMed PubMed Citation Articles by Harada, N. Articles by Inagaki, N.

A novel GIP receptor splice variant influences GIP sensitivity of pancreatic β-cells in obese mice

¹Department of Diabetes and Clinical Nutrition, Kyoto University Graduate School of Medicine, Kyoto; ²Japan Association for the Advancement of Medical Equipment, Tokyo; ³Kansai Electric Power Hospital, Osaka; and ⁴Core Research for Evolutional Science and Technology of Japan Science and Technology, Kyoto, Japan

Submitted 11 June 2007 ; accepted in final form 11 October 2007

Gastric inhibitory polypeptide (GIP) is an incretin that potentiates insulin secretion from pancreatic β-cells by binding to GIP receptor (GIPR) and subsequently increasing the level of intracellular adenosine 3',5'-cyclic monophosphate (cAMP). We have identified a novel GIPR splice variant in mouse β-cells that retains intron 8, resulting in a COOH-terminal truncated form (truncated GIPR). This isoform was coexpressed with full-length GIPR (wild-type GIPR) in normal GIPR-expressing tissues. In an experiment using cells transfected with both GIPRs, truncated GIPR did not lead to cAMP production induced by GIP but inhibited GIP-induced cAMP production through wild-type GIPR (n = 3–4, P < 0.05). Wild-type GIPR was normally located on the cell surface, but its expression was decreased in the presence of truncated GIPR, suggesting a dominant negative effect of truncated GIPR against wild-type GIPR. The functional relevance of truncated GIPR in vivo was investigated. In high-fat diet-fed obese mice (HFD mice), blood glucose levels were maintained by compensatory increased insulin secretion (n = 8, P < 0.05), and cAMP production (n = 6, P < 0.01) and insulin secretion (n = 10, P < 0.05) induced by GIP were significantly increased in isolated islets, suggesting hypersensitivity of the GIPR. Total GIPR mRNA expression was not increased in the islets of HFD mice, but the expression ratio of truncated GIPR to total GIPR was reduced by 32% compared with that of control mice (n = 6, P < 0.05). These results indicate that a relative reduction of truncated GIPR expression may be involved in hypersensitivity of GIPR and hyperinsulinemia in diet-induced obese mice.

gastric inhibitory polypeptide; gastric inhibitory polypeptide receptor; alternative splicing; dominant negative effect; obesity

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