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
  • [21] INTERLEUKIN-1-BETA MODULATES THE GROWTH AND PHENOTYPE OF NEONATAL RAT CARDIAC MYOCYTES
    THAIK, CM
    CALDERONE, A
    TAKAHASHI, N
    COLUCCI, WS
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (02) : 1093 - 1099
  • [22] PATHOLOGICAL HYPERTROPHY AND CARDIAC INTERSTITIUM - FIBROSIS AND RENIN-ANGIOTENSIN-ALDOSTERONE SYSTEM
    WEBER, KT
    BRILLA, CG
    [J]. CIRCULATION, 1991, 83 (06) : 1849 - 1865
  • [23] Cardiotrophin-1 and the role of gp130-dependent signaling pathways in cardiac growth and development
    Wollert, KC
    Chien, KR
    [J]. JOURNAL OF MOLECULAR MEDICINE-JMM, 1997, 75 (07): : 492 - 501
  • [24] Cardiotrophin-1 activates a distinct form of cardiac muscle cell hypertrophy - Assembly of sarcomeric units in series via gp130 leukemia inhibitory factor receptor-dependent pathways
    Wollert, KC
    Taga, T
    Saito, M
    Narazaki, M
    Kishimoto, T
    Glembotski, CC
    Vernallis, AB
    Heath, JK
    Pennica, D
    Wood, WI
    Chien, KR
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (16) : 9535 - 9545
  • [25] YAMAZAKI T, 1995, HERZ, V20, P109
  • [26] Targeted disruption of gp130, a common signal transducer for the interleukin 6 family of cytokines, leads to myocardial and hematological disorders
    Yoshida, K
    Taga, T
    Saito, M
    Suematsu, S
    Kumanogoh, A
    Tanaka, T
    Fujiwara, H
    Hirata, M
    Yamagami, T
    Nakahata, T
    Hirabayashi, T
    Yoneda, Y
    Tanaka, K
    Wang, WZ
    Mori, C
    Shiota, K
    Yoshida, N
    Kishimoto, T
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (01) : 407 - 411