GUINEA-PIG GALLBLADDER AND PANCREAS POSSESS IDENTICAL CCK-A RECEPTOR SUBTYPES - RECEPTOR CLONING AND EXPRESSION

被引:40
作者
DEWEERTH, A [1 ]
PISEGNA, JR [1 ]
WANK, SA [1 ]
机构
[1] NIADDKD, DIGEST DIS BRANCH,BLDG 10,RM 9C103, 9000 ROCKVILLE PIKE, BETHESDA, MD 20892 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1993年 / 265卷 / 06期
关键词
CHOLECYSTOKININ;
D O I
10.1152/ajpgi.1993.265.6.G1116
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Cholecystokinin (CCK) receptors mediate pancreatic acinar secretion and gallbladder contraction. Pharmacological and functional studies in pancreas and gallbladder demonstrate a CCK-A receptor subtype in both tissues. However, some pharmacological studies and affinity cross-linking studies of CCK receptors on pancreatic acini and gallbladder suggest that these two tissues possess two different subtypes of the CCK-A receptor. We cloned these receptors in guinea pig using a cDNA clone of the CCK-A receptor from rat pancreas. The guinea pig gallbladder CCK-A receptor was cloned by hybridization screening of a gallbladder cDNA library using a cDNA probe from the rat CCK-A receptor coding region. The guinea pig pancreas CCK-A receptor cDNA was cloned via the polymerase chain reaction using primers corresponding to the guinea pig gallbladder CCK-A receptor 5'- and 3'-noncoding regions. CCK-A receptor clones from guinea pig pancreas and gallbladder had identical nucleotide sequences, which were 80% homologous to the rat CCK-A receptor cDNA sequence. The deduced amino acid sequence from guinea pig CCK-A receptors was 89% homologous to the rat CCK-A receptor sequence. Dose-inhibition binding studies of transiently expressed receptors by CCK agonists and antagonists exhibited a CCK-A receptor pharmacologically similar to the rat CCK-A receptor. These studies indicate that the CCK-A receptors in guinea pig pancreas and gallbladder are identical and do not support previous proposals that they may represent different receptor subtypes.
引用
收藏
页码:G1116 / G1121
页数:6
相关论文
共 37 条
  • [2] CHOVDHURY J, 1975, EXPERIENTIA, V32, P1173
  • [3] CULLEN BR, 1987, METHOD ENZYMOL, V152, P684
  • [4] DAVIS LG, 1986, BASIC METHODS MOL BI, P1
  • [5] A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX
    DEVEREUX, J
    HAEBERLI, P
    SMITHIES, O
    [J]. NUCLEIC ACIDS RESEARCH, 1984, 12 (01) : 387 - 395
  • [6] STRUCTURAL FEATURES REQUIRED FOR LIGAND-BINDING TO THE BETA-ADRENERGIC-RECEPTOR
    DIXON, RAF
    SIGAL, IS
    CANDELORE, MR
    REGISTER, RB
    SCATTERGOOD, W
    RANDS, E
    STRADER, CD
    [J]. EMBO JOURNAL, 1987, 6 (11) : 3269 - 3275
  • [7] ISOLATION OF FULL-LENGTH PUTATIVE RAT LYSOPHOSPHOLIPASE CDNA USING IMPROVED METHODS FOR MESSENGER-RNA ISOLATION AND CDNA CLONING
    HAN, JH
    STRATOWA, C
    RUTTER, WJ
    [J]. BIOCHEMISTRY, 1987, 26 (06) : 1617 - 1625
  • [8] MUSCARINIC RECEPTOR SUBTYPES
    HULME, EC
    BIRDSALL, NJM
    BUCKLEY, NJ
    [J]. ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1990, 30 : 633 - 673
  • [9] JENSEN RT, 1989, ELLIS HOR S, P150
  • [10] INTERACTION OF CHOLECYSTOKININ WITH SPECIFIC MEMBRANE-RECEPTORS ON PANCREATIC ACINAR-CELLS
    JENSEN, RT
    LEMP, GF
    GARDNER, JD
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (04): : 2079 - 2083