Probing cell type-specific functions of Gi in vivo identifies GPCR regulators of insulin secretion

Jean B. Regard, Hiroshi Kataoka, David A. Cano, Eric Camerer, Liya Yin, Yao Wu Zheng, Thomas (Tom) Scanlan, Matthias Hebrok, Shaun R. Coughlin

Research output: Contribution to journalArticle

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Abstract

The in vivo roles of the hundreds of mammalian G protein-coupled receptors (GPCRs) are incompletely understood. To explore these roles, we generated mice expressing the S1 subunit of pertussis toxin, a known inhibitor of G i/o signaling, under the control of the ROSA26 locus in a Cre recombinase-dependent manner (ROSA26PTX). Crossing ROSA26 PTX mice to mice expressing Cre in pancreatic β cells produced offspring with constitutive hyperinsulinemia, increased insulin secretion in response to glucose, and resistance to diet-induced hyperglycemia. This phenotype underscored the known importance of Gi/o and hence of GPCRs for regulating insulin secretion. Accordingly, we quantified mRNA for each of the approximately 373 nonodorant GPCRs in mouse to identify receptors highly expressed in islets and examined the role of several. We report that 3-iodothyronamine, a thyroid hormone metabolite, could negatively and positively regulate insulin secretion via the Gi-coupled α2A- adrenergic receptor and the Gs-coupled receptor Taar1, respectively, and protease-activated receptor-2 could negatively regulate insulin secretion and may contribute to physiological regulation of glucose metabolism. The ROSA26PTX system used in this study represents a new genetic tool to achieve tissue-specific signaling pathway modulation in vivo that can be applied to investigate the role of Gi/o-coupled GPCRs in multiple cell types and processes.

Original languageEnglish (US)
Pages (from-to)4034-4043
Number of pages10
JournalJournal of Clinical Investigation
Volume117
Issue number12
DOIs
StatePublished - Dec 2007

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G-Protein-Coupled Receptors
Insulin
PAR-2 Receptor
Glucose
Internal-External Control
Hyperinsulinism
Thyroid Hormones
Hyperglycemia
Adrenergic Receptors
Diet
Phenotype
Messenger RNA

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Regard, J. B., Kataoka, H., Cano, D. A., Camerer, E., Yin, L., Zheng, Y. W., ... Coughlin, S. R. (2007). Probing cell type-specific functions of Gi in vivo identifies GPCR regulators of insulin secretion. Journal of Clinical Investigation, 117(12), 4034-4043. https://doi.org/10.1172/JCI32994

Probing cell type-specific functions of Gi in vivo identifies GPCR regulators of insulin secretion. / Regard, Jean B.; Kataoka, Hiroshi; Cano, David A.; Camerer, Eric; Yin, Liya; Zheng, Yao Wu; Scanlan, Thomas (Tom); Hebrok, Matthias; Coughlin, Shaun R.

In: Journal of Clinical Investigation, Vol. 117, No. 12, 12.2007, p. 4034-4043.

Research output: Contribution to journalArticle

Regard, JB, Kataoka, H, Cano, DA, Camerer, E, Yin, L, Zheng, YW, Scanlan, TT, Hebrok, M & Coughlin, SR 2007, 'Probing cell type-specific functions of Gi in vivo identifies GPCR regulators of insulin secretion', Journal of Clinical Investigation, vol. 117, no. 12, pp. 4034-4043. https://doi.org/10.1172/JCI32994
Regard, Jean B. ; Kataoka, Hiroshi ; Cano, David A. ; Camerer, Eric ; Yin, Liya ; Zheng, Yao Wu ; Scanlan, Thomas (Tom) ; Hebrok, Matthias ; Coughlin, Shaun R. / Probing cell type-specific functions of Gi in vivo identifies GPCR regulators of insulin secretion. In: Journal of Clinical Investigation. 2007 ; Vol. 117, No. 12. pp. 4034-4043.
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