Production and secretion of adrenomedullin in cultured rat cardiac myocytes and nonmyocytes:: Stimulation by interleukin-1β and tumor necrosis factor-α

被引:84
作者
Horio, T
Nishikimi, T
Yoshihara, F
Nagaya, N
Matsuo, H
Takishita, S
Kangawa, K
机构
[1] Natl Cardiovasc Ctr, Dept Med, Div Hypertens, Suita, Osaka 5658565, Japan
[2] Natl Cardiovasc Ctr, Inst Res, Suita, Osaka 5658565, Japan
关键词
D O I
10.1210/en.139.11.4576
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The present study investigated the secretion level and gene expression of adrenomedullin (AM), a novel vasorelaxant peptide, in cultured neonatal rat cardiac myocytes and nonmyocytes, and the effects of interleukin-1 beta (IL-1 beta) and tumor necrosis factor-alpha (TNF alpha) on its production and secretion in these cells. Under serum-free conditions, both myocytes and nonmyocytes secreted immunoreactive (ir-) AM into the culture medium in a time-dependent manner. The secretion rates of ir-AM from myocytes and nonmyocytes per 10(5) cells were almost equivalent. The expression of AM messenger RNA was also observed in cultured myocytes and nonmyocytes. The peptide secretion and messenger RNA level of AM in cardiac myocytes were increased after stimulation with IL-1 beta. In nonmyocytes, IL-1 beta and TNF alpha remarkably augmented both the release of ir-AM into the medium and AM gene expression after 24 and 48 h of incubation. These observations indicate that cardiac ventricular cells (i.e. myocytes and nonmyocytes) actively produce AM: and also suggest that cytokines such as IL-1 beta and TNF alpha regulate the gene expression and secretion of this peptide in the ventricles. On the basis of these results and the findings that IL-1 beta and TNF alpha are involved in heart failure and cardiac hypertrophy, AM may play a role as an autocrine/paracrine modulator in some cardiac disorders.
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收藏
页码:4576 / 4580
页数:5
相关论文
共 37 条
[1]   DISTRIBUTION AND MOLECULAR-FORMS OF BRAIN NATRIURETIC PEPTIDE IN THE CENTRAL NERVOUS-SYSTEM, HEART AND PERIPHERAL TISSUE OF RAT [J].
ABURAYA, M ;
MINAMINO, N ;
HINO, J ;
KANGAWA, K ;
MATSUO, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 165 (02) :880-887
[2]   INTERLEUKIN-1 PRETREATMENT DECREASES ISCHEMIA REPERFUSION INJURY [J].
BROWN, JM ;
WHITE, CW ;
TERADA, LS ;
GROSSO, MA ;
SHANLEY, PF ;
MULVIN, DW ;
BANERJEE, A ;
WHITMAN, GJR ;
HARKEN, AH ;
REPINE, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (13) :5026-5030
[3]  
DUTKA DP, 1993, BRIT HEART J, V70, P141
[4]   TUMOR-NECROSIS-FACTOR-ALPHA PRETREATMENT IS PROTECTIVE IN A RAT MODEL OF MYOCARDIAL ISCHEMIA-REPERFUSION INJURY [J].
EDDY, LJ ;
GOEDDEL, DV ;
WONG, GHW .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 184 (02) :1056-1059
[5]   INTERLEUKIN-1-BETA MODULATES MYOCARDIAL-CONTRACTION VIA DEXAMETHASONE SENSITIVE PRODUCTION OF NITRIC-OXIDE [J].
EVANS, HG ;
LEWIS, MJ ;
SHAH, AM .
CARDIOVASCULAR RESEARCH, 1993, 27 (08) :1486-1490
[6]   NEGATIVE INOTROPIC EFFECTS OF CYTOKINES ON THE HEART MEDIATED BY NITRIC-OXIDE [J].
FINKEL, MS ;
ODDIS, CV ;
JACOB, TD ;
WATKINS, SC ;
HATTLER, BG ;
SIMMONS, RL .
SCIENCE, 1992, 257 (5068) :387-389
[7]  
Harada M, 1997, CIRCULATION, V96, P3737
[8]   ADRENOMEDULLIN AS A NOVEL ANTIMIGRATION FACTOR OF VASCULAR SMOOTH-MUSCLE CELLS [J].
HORIO, T ;
KOHNO, M ;
KANO, H ;
IKEDA, M ;
YASUNARI, K ;
YOKOKAWA, K ;
MINAMI, M ;
TAKEDA, T .
CIRCULATION RESEARCH, 1995, 77 (04) :660-664
[9]   Adrenomedullin augments inducible nitric oxide synthase expression in cytokine-stimulated cardiac myocytes [J].
Ikeda, U ;
Kanbe, T ;
Kawahara, Y ;
Yokoyama, M ;
Shimada, K .
CIRCULATION, 1996, 94 (10) :2560-2565
[10]   Negative inotropic effect of adrenomedullin in isolated adult rabbit cardiac ventricular myocytes [J].
Ikenouchi, H ;
Kangawa, K ;
Matsuo, H ;
Hirata, Y .
CIRCULATION, 1997, 95 (09) :2318-2324