Expression and distribution of Gpr119 in the pancreatic islets of mice and rats: Predominant localization in pancreatic polypeptide-secreting PP-cells

被引:90
作者
Sakamoto, Yukiko
Inoue, Hiroshi [1 ]
Kawakami, Shuhei
Miyawaki, Katsuyuki
Miyamoto, Tatsuro
Mizuta, Kuniko
Itakura, Mitsuo
机构
[1] Univ Tokushima, Inst Genome Res, Tokushima 770, Japan
[2] Univ Tokushima, Dept Ophthalmol & Visual Sci, Tokushima 770, Japan
[3] Hiroshima Univ, Grad Sch Biomed Sci, Div Cervicognathostomatol, Hiroshima, Japan
关键词
GPR119; oleoylethanolamide; pancreatic polypeptide;
D O I
10.1016/j.bbrc.2006.10.076
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The GPR119 was recently shown to be activated by oleoylethanolamide (OEA), a naturally occurring bioactive lipid with hypophagic and anti-obesity effects. In this study, we have cloned and characterized its murine counterpart, Gpr119. The full-length cDNA contained an open reading frame of 1008 bp encoding a 335-amino acid protein. The genomic organization of 6pr119 was unique, having a 3'-untranslated second exon that was also involved in an alternative splicing event. Gene expression analyses confirmed its specific expressions in pancreatic islets and two endocrine cell-lines, MIN6 and alpha TC1. Inummohistochemistry and double-immunofluorescence studies using a specific antibody revealed the predominant Gpr119 localization in pancreatic polypeptide (PP)-cells of islets. No definitive evidence of Gpr119-immunoreactivity in adult beta- or alpha-cells was obtained. The 6pr119 mRNA levels were elevated in islets of obese hyperglycemic db/db mice as compared to control islets, suggesting a possible involvement of this receptor in the development of obesity and diabetes. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:474 / 480
页数:7
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