gp130 signaling pathways: Recent advances and implications for cardiovascular disease

被引:13
作者
Hirota, H [1 ]
Yoshida, K [1 ]
Taga, T [1 ]
Kishimoto, T [1 ]
机构
[1] OSAKA UNIV, INST MOLEC & CELLULAR BIOL, OSAKA, JAPAN
关键词
D O I
10.1016/1050-1738(96)00037-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
gp130 was initially identified as a signal-transducing receptor component that associates with the interleukin 6 receptor (IL-6R) when the receptor is occupied by interleukin 6 (IL-6). It has been revealed that the receptor complexes for IL-6, IL-11, leukemia inhibitory factor (LIF), oncostatin M (OM), and ciliary neurotrophic factor (CNTF) utilize this gp130 protein as a common signal-transducing component, explaining how these cytokines mediate overlapping biological function. Recent observations with mice lacking gp 130 or having continuously activated gp130 protein have disclosed an important biological function of gp130 in cardiovascular system: the former mice show extremely hypoplastic development of the ventricular myocardium at 16.5 days postcoitum (dpc), and the latter exhibit hypertrophy of myocardium. These cardiovascular abnormalities ave considered to be the results of the perturbation of gp130, which also transduces the signal of cardiotrophin-1 (CT-1), a recently isolated factor causing hypertrophy in cultured cardiomyocytes and having sequence similarity with IL-6, IL-11, LIF, CNTF, and OM. In fact, CT-1 shaves gp130 with these cytokines as a critical signaling component. Besides various well-established mechanisms by which cardiac growth and development are regulated a gp130 signaling may be a newly discovered mechanism that regulates these events.
引用
收藏
页码:109 / 115
页数:7
相关论文
共 58 条
[1]   CHOLINERGIC NEURONOTROPIC FACTORS - INTRA-OCULAR DISTRIBUTION OF TROPHIC ACTIVITY FOR CILIARY NEURONS [J].
ADLER, R ;
LANDA, KB ;
MANTHORPE, M ;
VARON, S .
SCIENCE, 1979, 204 (4400) :1434-1436
[2]   MOLECULAR-CLONING OF APRF, A NOVEL IFN-STIMULATED GENE FACTOR-3 P91-RELATED TRANSCRIPTION FACTOR INVOLVED IN THE GP130-MEDIATED SIGNALING PATHWAY [J].
AKIRA, S ;
NISHIO, Y ;
INOUE, M ;
WANG, XJ ;
WEI, S ;
MATSUSAKA, T ;
YOSHIDA, K ;
SUDO, T ;
NARUTO, M ;
KISHIMOTO, T .
CELL, 1994, 77 (01) :63-71
[3]   SHARED ARCHITECTURE OF HORMONE BINDING DOMAINS IN TYPE-I AND TYPE-II INTERFERON RECEPTORS [J].
BAZAN, JF .
CELL, 1990, 61 (05) :753-754
[4]  
BOGOYEVITCH MA, 1994, J BIOL CHEM, V269, P1110
[5]  
BROWN TJ, 1991, J IMMUNOL, V147, P2175
[6]  
CHAO TSO, 1994, J BIOL CHEM, V269, P7337
[7]  
CONOVER JC, 1993, DEVELOPMENT, V119, P559
[8]   REQUIREMENT FOR MAP KINASE (ERK2) ACTIVITY IN INTERFERON-ALPHA-STIMULATED AND INTERFERON-BETA-STIMULATED GENE-EXPRESSION THROUGH STAT PROTEINS [J].
DAVID, M ;
PETRICOIN, E ;
BENJAMIN, C ;
PINE, R ;
WEBER, MJ ;
LARNER, AC .
SCIENCE, 1995, 269 (5231) :1721-1723
[9]   LIFR-BETA AND GP-130 AS HETERODIMERIZING SIGNAL TRANSDUCERS OF THE TRIPARTITE CNTF RECEPTOR [J].
DAVIS, S ;
ALDRICH, TH ;
STAHL, N ;
PAN, L ;
TAGA, T ;
KISHIMOTO, T ;
IP, NY ;
YANCOPOULOS, GD .
SCIENCE, 1993, 260 (5115) :1805-1808
[10]   NEUROPOIETIC CYTOKINES AND ACTIVIN-A DIFFERENTIALLY REGULATE THE PHENOTYPE OF CULTURED SYMPATHETIC NEURONS [J].
FANN, MJ ;
PATTERSON, PH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (01) :43-47