Gut-expressed gustducin and taste receptors regulate secretion of glucagon-like peptide-1

Glucagon-like peptide-1 (GLP-1), released from gut endocrine L cells in response to glucose, regulates appetite, insulin secretion, and gut motility. How glucose given orally, but not systemically, induces GLP-1 secretion is unknown. We show that human duodenal L cells express sweet taste receptors,...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 2007-09, Vol.104 (38), p.15069-15074
Hauptverfasser: Jang, Hyeung-Jin, Kokrashvili, Zaza, Theodorakis, Michael J, Carlson, Olga D, Kim, Byung-Joon, Zhou, Jie, Kim, Hyeon Ho, Xu, Xiangru, Chan, Sic L, Juhaszova, Magdalena, Bernier, Michel, Mosinger, Bedrich, Margolskee, Robert F, Egan, Josephine M
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Sprache:eng
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Zusammenfassung:Glucagon-like peptide-1 (GLP-1), released from gut endocrine L cells in response to glucose, regulates appetite, insulin secretion, and gut motility. How glucose given orally, but not systemically, induces GLP-1 secretion is unknown. We show that human duodenal L cells express sweet taste receptors, the taste G protein gustducin, and several other taste transduction elements. Mouse intestinal L cells also express α-gustducin. Ingestion of glucose by α-gustducin null mice revealed deficiencies in secretion of GLP-1 and the regulation of plasma insulin and glucose. Isolated small bowel and intestinal villi from α-gustducin null mice showed markedly defective GLP-1 secretion in response to glucose. The human L cell line NCI-H716 expresses α-gustducin, taste receptors, and several other taste signaling elements. GLP-1 release from NCI-H716 cells was promoted by sugars and the noncaloric sweetener sucralose, and blocked by the sweet receptor antagonist lactisole or siRNA for α-gustducin. We conclude that L cells of the gut "taste" glucose through the same mechanisms used by taste cells of the tongue. Modulating GLP-1 secretion in gut "taste cells" may provide an important treatment for obesity, diabetes and abnormal gut motility.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.0706890104