AGONIST REGULATION OF CELLULAR G-PROTEIN LEVELS AND DISTRIBUTION - MECHANISMS AND FUNCTIONAL IMPLICATIONS

被引:126
作者
MILLIGAN, G [1 ]
机构
[1] UNIV GLASGOW, DEPT PHARMACOL, MOLEC PHARMACOL GRP, GLASGOW G12 8QQ, SCOTLAND
基金
英国惠康基金;
关键词
D O I
10.1016/0165-6147(93)90064-Q
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Exposure of cells to agonists of receptors linked to G proteins can result in downregulation of cellular levels or redistribution of G proteins from membranes to the cytosol. Agonist-induced reductions in G protein levels have been observed for members of each of the G(s), G(i) and G(q) families of G proteins, are likely to be dependent upon the level of receptor expression, and are generally restricted to the G protein(s) with which the receptor interacts. The mechanisms responsible, reviewed here by Graeme Milligan, vary with cell type and include both second messenger-dependent and -independent enhanced protein degradation. Agonist-induced reduction in cellular G protein levels can provide one mechanism for the development of sustained heterologous desensitization.
引用
收藏
页码:413 / 418
页数:6
相关论文
共 43 条
[1]   CONCURRENT DOWN-REGULATION OF IP PROSTANOID RECEPTORS AND THE ALPHA-SUBUNIT OF THE STIMULATORY GUANINE-NUCLEOTIDE-BINDING PROTEIN (GS) DURING PROLONGED EXPOSURE OF NEUROBLASTOMA X GLIOMA-CELLS TO PROSTANOID AGONISTS - QUANTIFICATION AND FUNCTIONAL IMPLICATIONS [J].
ADIE, EJ ;
MULLANEY, I ;
MCKENZIE, FR ;
MILLIGAN, G .
BIOCHEMICAL JOURNAL, 1992, 285 :529-536
[2]   AGONIST REGULATION OF CELLULAR-LEVELS OF THE STIMULATORY GUANINE-NUCLEOTIDE-BINDING PROTEIN, G(S), IN WILD-TYPE AND TRANSFECTED NEUROBLASTOMA-GLIOMA HYBRID NG108-15 CELLS [J].
ADIE, EJ ;
MILLIGAN, G .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1993, 21 (02) :432-435
[3]   STOICHIOMETRY OF RECEPTOR-GS-ADENYLATE CYCLASE INTERACTIONS [J].
ALOUSI, AA ;
JASPER, JR ;
INSEL, PA ;
MOTULSKY, HJ .
FASEB JOURNAL, 1991, 5 (09) :2300-2303
[4]   PHOSPHOLIPASE C-BETA-1 IS A GTPASE-ACTIVATING PROTEIN FOR GQ/11, ITS PHYSIOLOGICAL REGULATOR [J].
BERSTEIN, G ;
BLANK, JL ;
JHON, DY ;
EXTON, JH ;
RHEE, SG ;
ROSS, EM .
CELL, 1992, 70 (03) :411-418
[5]  
CAMPBELL PT, 1991, MOL PHARMACOL, V39, P192
[6]  
CHANG FH, 1989, J BIOL CHEM, V264, P5352
[7]   MODEL SYSTEMS FOR THE STUDY OF 7-TRANSMEMBRANE-SEGMENT RECEPTORS [J].
DOHLMAN, HG ;
THORNER, J ;
CARON, MG ;
LEFKOWITZ, RJ .
ANNUAL REVIEW OF BIOCHEMISTRY, 1991, 60 :653-688
[8]   GS-ALPHA IS A SUBSTRATE FOR MONO(ADP-RIBOSYL)TRANSFERASE OF NG108-15 CELLS - ADP-RIBOSYLATION REGULATES GS-ALPHA ACTIVITY AND ABUNDANCE [J].
DONNELLY, LE ;
BOYD, RS ;
MACDERMOT, J .
BIOCHEMICAL JOURNAL, 1992, 288 :331-336
[9]  
EASON MG, 1992, J BIOL CHEM, V267, P25473
[10]   PROSTACYCLIN ANALOGS REDUCE ADP-RIBOSYLATION OF THE ALPHA-SUBUNIT OF THE REGULATORY GS-PROTEIN AND DIMINISH ADENOSINE (A2) RESPONSIVENESS OF PLATELETS [J].
EDWARDS, RJ ;
MACDERMOT, J ;
WILKINS, AJ .
BRITISH JOURNAL OF PHARMACOLOGY, 1987, 90 (03) :501-510