Colocalization of the α-subunit of gustducin with PYY and GLP-1 in L cells of human colon

被引:217
|
作者
Rozengurt, Nora
Wu, S. Vincent
Chen, Monica C.
Huang, Carlos
Sternini, Catia
Rozengurt, Enrique
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Ctr Ulcer Res & Educ, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Digest Dis Res Ctr, Los Angeles, CA 90095 USA
关键词
type 2 receptor family; gastrointestinal peptides; peptide YY; glucagon-like peptide-1; chromogranin A; serotonin; phenylthiocarbamide;
D O I
10.1152/ajpgi.00074.2006
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
In view of the importance of molecular sensing in the function of the gastrointestinal (GI) tract, we assessed whether signal transduction proteins that mediate taste signaling are expressed in cells of the human gut. Here, we demonstrated that the alpha-subunit of the taste-specific G protein gustducin (G alpha(gust)) is expressed prominently in cells of the human colon that also contain chromogranin A, an established marker of endocrine cells. Double-labeling immunofluorescence and staining of serial sections demonstrated that G alpha(gust) localized to enteroendocrine L cells that express peptide YY and glucagon-like peptide-1 in the human colonic mucosa. We also found expression of transcripts encoding human type 2 receptor (hT2R) family members, hT1R3, and G alpha(gust) in the human colon and in the human intestinal endocrine cell lines (HuTu-80 and NCI-H716 cells). Stimulation of HuTu-80 or NCI-H716 cells with the bitter-tasting compound phenylthiocarbamide, which binds hT2R38, induced a rapid increase in the intracellular Ca2+ concentration in these cells. The identification of G alpha(gust) and chemosensory receptors that perceive chemical components of ingested substances, including drugs and toxins, in open enteroendocrine L cells has important implications for understanding molecular sensing in the human GI tract and for developing novel therapeutic compounds that modify the function of these receptors in the gut.
引用
收藏
页码:G792 / G802
页数:11
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