G protein-coupled receptors and signaling pathways regulating growth responses

被引:204
作者
Post, GR [1 ]
Brown, JH [1 ]
机构
[1] UNIV CALIF SAN DIEGO,DEPT PHARMACOL,LA JOLLA,CA 92093
关键词
mitogenesis; gene expression; tyrosine phosphorylation; mitogen-activated protein kinases; Ras effectors; transformation; hypertrophy; c-Jun NH2-terminal kinases;
D O I
10.1096/fasebj.10.7.8635691
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
Hormones that interact with seven-transmembrane spanning receptors, generally considered to be involved in acute signaling functions, also induce longer term effects on gene expression and cell growth, These genetic and proliferative effects can be induced by activation of receptors that signal through heterotrimeric GTP-binding proteins (G-proteins) of the G(q) family, pertussis toxin-sensitive G(i)/G(o) proteins, G(s), or G(12)/G(13). Numerous growth-promoting G protein-coupled receptors activate the low molecular weight G-protein Ras and stimulate mitogen-activated protein kinase, Recent data suggest that c-Jun NH2-terminal kinase is also activated, possibly through interaction with low molecular weight G-proteins of the Rho family, Because G protein-coupled receptors lack intrinsic tyrosine kinase activity, the mechanisms by which heterotrimeric G-proteins couple to these kinase cascades remain to be elucidated, By analogy to growth factor receptors, G protein-coupled receptors may access these kinase cascades through binding of adapter proteins or recruitment of cytosolic tyrosine kinases, It is likely that interactions between multiple signaling pathways are required for G protein-coupled receptors to propagate signals to the nucleus.
引用
收藏
页码:741 / 749
页数:9
相关论文
共 137 条
[31]  
FAURE M, 1994, J BIOL CHEM, V269, P7851
[32]   MITOGEN-ACTIVATED PROTEIN-KINASE ACTIVATION RESULTING FROM SELECTIVE ONCOGENE EXPRESSION IN NIH-3T3 AND RAT-1A CELLS [J].
GALLEGO, C ;
GUPTA, SK ;
HEASLEY, LE ;
QIAN, NX ;
JOHNSON, GL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (16) :7355-7359
[33]   ESTABLISHMENT OF A NORADRENERGIC CLONAL LINE OF RAT ADRENAL PHEOCHROMOCYTOMA CELLS WHICH RESPOND TO NERVE GROWTH-FACTOR [J].
GREENE, LA ;
TISCHLER, AS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1976, 73 (07) :2424-2428
[34]   TRANSCRIPTION FACTOR ATF2 REGULATION BY THE JNK SIGNAL-TRANSDUCTION PATHWAY [J].
GUPTA, S ;
CAMPBELL, D ;
DERIJARD, B ;
DAVIS, RJ .
SCIENCE, 1995, 267 (5196) :389-393
[35]   ANALYSIS OF THE FIBROBLAST TRANSFORMATION POTENTIAL OF GTPASE-DEFICIENT GIP2 ONCOGENES [J].
GUPTA, SK ;
GALLEGO, C ;
LOWNDES, JM ;
PLEIMAN, CM ;
SABLE, C ;
EISFELDER, BJ ;
JOHNSON, GL .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (01) :190-197
[36]  
GUSOVSKY F, 1993, J BIOL CHEM, V268, P7768
[37]  
GUTKIND JS, 1992, BIOCHEM BIOPH RES CO, V188, P155
[38]   MUSCARINIC ACETYLCHOLINE-RECEPTOR SUBTYPES AS AGONIST-DEPENDENT ONCOGENES [J].
GUTKIND, JS ;
NOVOTNY, EA ;
BRANN, MR ;
ROBBINS, KC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (11) :4703-4707
[39]   LOCALIZATION OF A HETEROTRIMERIC G-PROTEIN GAMMA-SUBUNIT TO FOCAL ADHESIONS AND ASSOCIATED STRESS FIBERS [J].
HANSEN, CA ;
SCHROERING, AG ;
CAREY, DJ ;
ROBISHAW, JD .
JOURNAL OF CELL BIOLOGY, 1994, 126 (03) :811-819
[40]   DISTINCT PATHWAYS OF G(I)-MEDIATED AND G(Q)-MEDIATED MITOGEN-ACTIVATED PROTEIN-KINASE ACTIVATION [J].
HAWES, BE ;
VANBIESEN, T ;
KOCH, WJ ;
LUTTRELL, LM ;
LEFKOWITZ, RJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (29) :17148-17153