Involvement of cardiotrophin-1 in cardiac myocyte-nonmyocyte interactions during hypertrophy of rat cardiac myocytes in vitro

被引:110
作者
Kuwahara, K [1 ]
Saito, Y [1 ]
Harada, M [1 ]
Ishikawa, M [1 ]
Ogawa, E [1 ]
Miyamoto, Y [1 ]
Hamanaka, I [1 ]
Kamitani, S [1 ]
Kajiyama, N [1 ]
Takahashi, N [1 ]
Nakagawa, O [1 ]
Masuda, I [1 ]
Nakao, K [1 ]
机构
[1] Kyoto Univ, Grad Sch Med, Dept Med & Clin Sci, Sakyo Ku, Kyoto 606, Japan
关键词
hypertrophy; natriuretic peptides; cells; antibodies; interleukin;
D O I
10.1161/01.CIR.100.10.1116
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-The mechanism responsible for cardiac hypertrophy is currently conceptualized as having 2 components, mediated by cardiac myocytes and nonmyocytes, respectively. The interaction between myocytes and nonmyocytes via growth factors and/or cytokines plays an important role in the development of cardiac hypertrophy. We found that cardiac myocytes showed hypertrophic changes when cocultured with cardiac nonmyocytes. Cardiotrophin-1 (CT-1), a new member of the interleukin-6 family of cytokines, was identified by its ability to induce hypertrophic response in cardiac myocytes. In this study, we used the in vitro coculture system to examine how CT-1 is involved in the interaction between cardiac myocytes and nonmyocytes during the hypertrophy process. Methods and Results-RNase protection assay revealed that CT-1 mRNA levels were 3.5 times higher in cultured cardiac nonmyocytes than in cultured cardiac myocytes. We developed anti-CT-1 antibodies and found that they significantly inhibited the increased atrial and brain natriuretic peptide secretion and protein synthesis characteristic of hypertrophic changes of myocytes in the coculture. In addition, non-myocyte-conditioned medium rapidly elicited tyrosine phosphorylation of STAT3 and induced an increase in natriuretic peptide secretion and protein synthesis in cultured cardiac myocytes; these effects were partially suppressed by anti-CT-1 antibodies. Finally, the;hypertrophic effects of CT-1 and endothelin-1, which we had previously implicated in the hypertrophic activity in the coculture, were additive in cardiac myocytes. Conclusions-These results show that CT-1 secreted from cardiac nonmyocytes is significantly involved in the hypertrophic changes of cardiac myocytes in the coculture and suggest that CT-1 is an important local regulator in the process of cardiac hypertrophy.
引用
收藏
页码:1116 / 1124
页数:9
相关论文
共 26 条
[1]   ENDOTHELIN INCREASES THE SYNTHESIS AND SECRETION OF ATRIAL-NATRIURETIC-PEPTIDE IN NEONATAL RAT CARDIOCYTES [J].
GARDNER, DG ;
NEWMAN, ED ;
NAKAMURA, KK ;
NGUYEN, KPT .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 261 (02) :E177-E182
[2]  
Harada M, 1997, CIRCULATION, V96, P3737
[3]   CONTINUOUS ACTIVATION OF GP130, A SIGNAL-TRANSDUCING RECEPTOR COMPONENT FOR INTERLEUKIN 6-RELATED CYTOKINES, CAUSES MYOCARDIAL HYPERTROPHY IN MICE [J].
HIROTA, H ;
YOSHIDA, K ;
KISHIMOTO, T ;
TAGA, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (11) :4862-4866
[4]   cDNA cloning of rat cardiotrophin-1 (CT-1): Augmented expression of CT-1 gene in ventricle of genetically hypertensive rats [J].
Ishikawa, M ;
Saito, Y ;
Miyamoto, Y ;
Kuwahara, K ;
Ogawa, E ;
Nakagawa, O ;
Harada, M ;
Masuda, I ;
Nakao, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 219 (02) :377-381
[5]   ENDOTHELIN-1 IS AN AUTOCRINE PARACRINE FACTOR IN THE MECHANISM OF ANGIOTENSIN-II-INDUCED HYPERTROPHY IN CULTURED RAT CARDIOMYOCYTES [J].
ITO, H ;
HIRATA, Y ;
ADACHI, S ;
TANAKA, M ;
TSUJINO, M ;
KOIKE, A ;
NOGAMI, A ;
MARUMO, F ;
HIROE, M .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (01) :398-403
[6]   INSULIN-LIKE GROWTH FACTOR-I INDUCES HYPERTROPHY WITH ENHANCED EXPRESSION OF MUSCLE-SPECIFIC GENES IN CULTURED RAT CARDIOMYOCYTES [J].
ITO, H ;
HIROE, M ;
HIRATA, Y ;
TSUJINO, M ;
ADACHI, S ;
SHICHIRI, M ;
KOIKE, A ;
NOGAMI, A ;
MARUMO, F .
CIRCULATION, 1993, 87 (05) :1715-1721
[7]   Cardiac fibroblasts produce leukemia inhibitory factor and endothelin, which combine to induce cardiac myocyte hypertrophy in vitro [J].
King, KL ;
Lai, J ;
Winer, J ;
Luis, E ;
Yen, R ;
Hooley, J ;
Williams, PM ;
Mather, JP .
ENDOCRINE, 1996, 5 (01) :85-93
[8]  
KNOWLTON KU, 1993, J BIOL CHEM, V268, P15374
[9]   BETA-ADRENERGIC STIMULATION OF CARDIAC NON-MYOCYTES AUGMENTS THE GROWTH-PROMOTING ACTIVITY OF NON-MYOCYTE CONDITIONED MEDIUM [J].
LONG, CS ;
HARTOGENSIS, WE ;
SIMPSON, PC .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1993, 25 (08) :915-925
[10]   ALPHA-1-ADRENERGIC RECEPTOR STIMULATION OF SARCOMERIC ACTIN ISOGENE TRANSCRIPTION IN HYPERTROPHY OF CULTURED RAT-HEART MUSCLE-CELLS [J].
LONG, CS ;
ORDAHL, CP ;
SIMPSON, PC .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 83 (03) :1078-1082