Tissue distribution of rat glucagon receptor and GLP-1 receptor gene expression

被引:139
作者
Dunphy, JL
Taylor, RG
Fuller, PJ
机构
[1] Prince Henrys Inst Med Res, Clayton, Vic 3168, Australia
[2] Monash Univ, Monash Med Ctr, Dept Med, Clayton, Vic 3168, Australia
[3] Royal Childrens Hosp, Dept Surg, Parkville, Vic 3052, Australia
关键词
glucagon receptor; GLP-1; receptor; proglucagon-derived peptides; nuclease protection assays; intestinal adaptation;
D O I
10.1016/S0303-7207(98)00096-3
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The regulation of glucose metabolism by glucagon and GLP-1 is well established, but novel functions for these and other proglucagon-derived peptides are less well defined. This paper highlights the diversity of both GLP-1 and glucagon activity by studying the tissue distribution of glucagon and GLP-1 receptor gene expression by both Southern blot analysis of RT-PCR products and nuclease protection assays. By Southern blot analysis of RT-PCR products, GLP-1 receptor mRNA was detected in lung, hypothalamus, hippocampus, cerebral cortex, kidney, pancreas, and throughout the gastrointestinal tract. Glucagon receptor expression was detected in liver, kidney, spleen, thymus, adrenal glands, pancreas, cerebral cortex, lung, and throughout the gastrointestinal tract. Nuclease protection assay revealed glucagon receptor expression to be highest in liver and kidney, whereas GLP-1 receptor expression was only detected by protection assay in lung, stomach, and large bowel. Despite previous evidence that other receptors for proglucagon-derived peptides may exist, no evidence of novel receptors or multiple isoforms of the glucagon and GLP-1 receptors was found, indicating that the two cloned receptors may mediate all the effects of proglucagon-derived peptides, or that novel receptors may share less homology with the glucagon and GLP-1 receptors than previously anticipated. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:179 / 186
页数:8
相关论文
共 32 条
  • [1] SYSTEMIC FACTORS ARE TROPHIC IN BYPASSED RAT SMALL-INTESTINE IN THE ABSENCE OF LUMINAL CONTENTS
    ALBERT, V
    YOUNG, GP
    MORTON, CL
    ROBINSON, P
    BHATHAL, PS
    [J]. GUT, 1990, 31 (03) : 311 - 316
  • [2] BLOOM SR, 1982, SCAND J GASTROENTERO, V17, P93
  • [3] BRISTOL JB, 1988, PEDIATR SURG INT, V4, P233
  • [4] GLUCAGON-CENTER-DOT-GLUCAGON-LIKE PEPTIDE-I RECEPTOR CHIMERAS REVEAL DOMAINS THAT DETERMINE SPECIFICITY OF GLUCAGON BINDING
    BUGGY, JJ
    LIVINGSTON, JN
    RABIN, DU
    YOOWARREN, H
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (13) : 7474 - 7478
  • [5] Tissue distribution of messenger ribonucleic acid encoding the rat glucagon-like peptide-1 receptor
    Bullock, BP
    Heller, RS
    Habener, JF
    [J]. ENDOCRINOLOGY, 1996, 137 (07) : 2968 - 2978
  • [6] CHIRGWIN JM, 1979, BIOCHEMISTRY-US, V18, P4294
  • [7] Induction of intestinal epithelial proliferation by glucagon-like peptide 2
    Drucker, DJ
    Ehrlich, P
    Asa, SL
    Brubaker, PL
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (15) : 7911 - 7916
  • [8] GLUCAGON-LIKE PEPTIDE-1(7-36) AMIDE (GLP-1) ENHANCES INSULIN-STIMULATED GLUCOSE-METABOLISM IN 3T3-L1 ADIPOCYTES - ONE OF SEVERAL POTENTIAL EXTRAPANCREATIC SITES OF GLP-1 ACTION
    EGAN, JM
    MONTROSERAFIZADEH, C
    WANG, YH
    BERNIER, M
    ROTH, J
    [J]. ENDOCRINOLOGY, 1994, 135 (05) : 2070 - 2075
  • [9] ILEAL PROGLUCAGON GENE-EXPRESSION IN THE RAT - CHARACTERIZATION IN INTESTINAL ADAPTATION USING INSITU HYBRIDIZATION
    FULLER, PJ
    BEVERIDGE, DJ
    TAYLOR, RG
    [J]. GASTROENTEROLOGY, 1993, 104 (02) : 459 - 466
  • [10] POU-DOMAIN GENE-EXPRESSION IN THE GASTROINTESTINAL-TRACT
    FULLER, PJ
    BEVERIDGE, DJ
    TAYLOR, RG
    [J]. JOURNAL OF CELLULAR BIOCHEMISTRY, 1995, 58 (02) : 260 - 267