Abstract

Several orphan G protein-coupled receptors, including GPR40, have recently been shown to be responsive to fatty acids. Although previous reports have suggested GPR40 detects medium- and long-chain fatty acids, it has been reported to be unresponsive to short chain fatty acids. In this study, we have heterologously expressed mouse GPR40 in Xenopus laevis oocytes and measured fatty acid-induced increases in intracellular Ca(2+), via two electrode voltage clamp recordings of the endogenous Ca(2+)-activated chloride conductance. Exposure to 500 muM linoleic acid (C18:2), a long-chain fatty acid, stimulated significant currents in mGPR40-injected oocytes (P < 0.01, ANOVA), but not in water-injected control oocytes (not significant, ANOVA). These currents were confirmed as Ca(2+)-activated chloride conductances because they were biphasic, sensitive to changes in external pH, and inhibited by DIDS. Similar currents were observed with medium-chain fatty acids, such as lauric acid (C12:0) (P < 0.01, ANOVA), and more importantly, with short-chain fatty acids, such as butyric acid (C4:0) (P < 0.01, ANOVA). In contrast, no responses were observed in mGPR40-injected oocytes exposed to either acetic acid (C2:0) or propionic acid (C3:0). Therefore, GPR40 has the capacity to respond to fatty acids with chain lengths of four or greater. This finding has important implications for understanding the structure:function relationship of fatty acid sensors, and potentially for short-chain fatty acid sensing in the gastrointestinal tract.

Highlights

  • G PROTEIN-COUPLED RECEPTORS (GPCRs) play a vital signaling role in numerous biological processes, with an ever-increasing number of endogenous physiological ligands

  • Increased pancreatic expression of GPR40 mRNA is observed in obese mice that lack leptin (13), whereas polymorphisms so far detected in the human GPR40 gene are not associated with abnormal insulin release (7)

  • GPR41 plays a role in leptin production in adipocytes (24), whereas GPR43 is implicated in differentiation and immune responses of monocytes and granulocytes (19)

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Summary

Introduction

G PROTEIN-COUPLED RECEPTORS (GPCRs) play a vital signaling role in numerous biological processes, with an ever-increasing number of endogenous physiological ligands. The functional evidence is strongest that GPR40 acts as the receptor for fatty acid-induced insulin secretion It is abundantly expressed in pancreatic ␤-cells (11), and GPR40 knockout and overexpression in vivo have been shown to mediate both acute and chronic effects of long-chain free fatty acids on murine insulin secretion (22). These data suggest that GPR40 may form a mechanistic link between diet, obesity, and Type 2 diabetes (22). We have previously reported (9) that STC-1 cells respond to fatty acids via mobilization of [Ca2ϩ]i, in a chain length-dependent pattern requiring 12 or more carbon atoms This suggests a possible role for GPR40 in fatty-acid sensing by STC-1 cells.

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