Intracellular third loop domain of angiotensin II type-2 receptor - Role in mediating signal transduction and cellular function

被引:97
作者
Hayashida, W [1 ]
Horiuchi, M [1 ]
Dzau, VJ [1 ]
机构
[1] STANFORD UNIV, SCH MED, FALK CARDIOVASC RES CTR, STANFORD, CA 94305 USA
关键词
D O I
10.1074/jbc.271.36.21985
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 present study tests the hypothesis that the unique intracellular third loop domain of angiotensin II type-2 (AT2) receptor is essential for the subsequent intracellular signaling and plays an important role in mediating receptor function, Synthetic intracellular third loop peptide of the AT2 receptor (AT2-3LP, 22 amino acids) and control peptide consisting of the same amino acid composition in random sequence were delivered into adult rat aortic vascular smooth muscle cells by cationic liposome-mediated transfection. Successful intracellular peptide delivery was confirmed by microscopic localization of the fluorescein-labeled AT2-3LP within the cells and also by co-immunoprecipitation of the I-125-labeled 3LP complexed with G(i) protein using anti-G(i) alpha antibody. The AT2-3LP-transfected cells showed reduction of serum-stimulated DNA synthesis and cell proliferation as well as a decrease in mitogen-activated protein kinase activity, simulating the effects of AT2 receptor stimulation. The antagonistic effect of the AT2-3LP on mitogen-activated protein kinase activity and DNA synthesis were reversed by pertussis toxin and sodium orthovanadate. Thus, our data suggest that the intracellular third loop domain of the AT2 receptor is closely linked with the cellular signaling pathways of vascular smooth muscle cells in which G(i) and protein-phosphotyrosine phosphatase are involved, resulting in the alteration of mitogen-activated protein kinase activity and in growth inhibition.
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页码:21985 / 21992
页数:8
相关论文
共 35 条
[1]   REQUIREMENT FOR INTEGRATION OF SIGNALS FROM 2 DISTINCT PHOSPHORYLATION PATHWAYS FOR ACTIVATION OF MAP KINASE [J].
ANDERSON, NG ;
MALLER, JL ;
TONKS, NK ;
STURGILL, TW .
NATURE, 1990, 343 (6259) :651-653
[2]   MUTATION OF ASP(74) OF THE RAT ANGIOTENSIN-II RECEPTOR CONFERS CHANGES IN ANTAGONIST AFFINITIES AND ABOLISHES G-PROTEIN COUPLING [J].
BIHOREAU, C ;
MONNOT, C ;
DAVIES, E ;
TEUTSCH, B ;
BERNSTEIN, KE ;
CORVOL, P ;
CLAUSER, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (11) :5133-5137
[3]   ANGIOTENSIN-II RECEPTOR SUBTYPES - CHARACTERIZATION, SIGNALING MECHANISMS, AND POSSIBLE PHYSIOLOGICAL IMPLICATIONS [J].
BOTTARI, SP ;
DEGASPARO, M ;
STECKELINGS, UM ;
LEVENS, NR .
FRONTIERS IN NEUROENDOCRINOLOGY, 1993, 14 (02) :123-171
[4]   A G-PROTEIN IS INVOLVED IN THE ANGIOTENSIN AT(2) RECEPTOR INHIBITION OF THE T-TYPE CALCIUM CURRENT IN NON-DIFFERENTIATED NG108-15 CELLS [J].
BUISSON, B ;
LAFLAMME, L ;
BOTTARI, SP ;
DEGASPARO, M ;
GALLOPAYET, N ;
PAYET, MD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (04) :1670-1674
[5]   STIMULATION OF TYROSINE PHOSPHATASE AND INHIBITION OF CELL-PROLIFERATION BY SOMATOSTATIN ANALOGS - MEDIATION BY HUMAN SOMATOSTATIN RECEPTOR SUBTYPES SSTR1 AND SSTR2 [J].
BUSCAIL, L ;
DELESQUE, N ;
ESTEVE, JP ;
SAINTLAURENT, N ;
PRATS, H ;
CLERC, P ;
ROBBERECHT, P ;
BELL, GI ;
LIEBOW, C ;
SCHALLY, AV ;
VAYSSE, N ;
SUSINI, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (06) :2315-2319
[6]  
CHAZENBALK GD, 1990, J BIOL CHEM, V265, P20970
[7]  
DALMAN HM, 1991, J BIOL CHEM, V266, P11025
[8]  
DEBS RJ, 1990, J BIOL CHEM, V265, P10189
[9]   CELL SIGNALING AND THE CONTROL OF GENE-TRANSCRIPTION [J].
EDWARDS, DR .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1994, 15 (07) :239-244
[10]   EFFECT OF 5-FLUORO-2'-DEOXYURIDINE (FDURD) ON 5-BROMO-2'-DEOXYURIDINE (BRDURD) INCORPORATION INTO DNA MEASURED WITH A MONOCLONAL BRDURD ANTIBODY AND BY THE BRDURD HOECHST QUENCHING EFFECT [J].
ELLWART, J ;
DORMER, P .
CYTOMETRY, 1985, 6 (06) :513-520