IGF I and bFGF differentially influence atrial natriuretic factor and alpha-smooth muscle actin expression in cultured atrial compared to ventricular adult rat cardiomyocytes

被引:35
作者
EppenbergerEberhardt, M
Aigner, S
Donath, MY
Kurer, V
Walther, P
Zuppinger, C
Schaub, MC
Eppenberger, HM
机构
[1] ETH ZURICH, INST CELL BIOL, SWISS FED INST TECHNOL, CH-8093 ZURICH, SWITZERLAND
[2] UNIV ZURICH HOSP, DEPT MED, CH-8091 ZURICH, SWITZERLAND
[3] UNIV ZURICH, INST PHARMACOL, CH-8057 ZURICH, SWITZERLAND
关键词
IGF-I; bFGF; ANF; alpha-smooth muscle actin; atrial adult cardiomyocytes; ventricular adult cardiomyocytes; adult cardiomyocytes in culture; MAP kinase;
D O I
10.1006/jmcc.1997.0408
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In the present study, we compare expression, storage and secretion of the atrial natriuretic factor (ANF) in atrial and ventricular adult rat cardiomyocytes (aARC and vARC) in long-term culture, The influence of insulin-like growth factor-I (IGF-I) and of basic fibroblast growth factor (bFGF) on ANF production and secretion, as well as on the expression of a structural component, alpha-smooth muscle actin (alpha-sm actin), was studied in the two cell types. Antibodies against alpha-ANF were used for immunocytochemical localization of ANF. aARC contained more ANF-granules than vARC, and they were distributed throughout the cell bodies. Quantitative determination of ANF storage and secretion was done by radioimmunoassay (RIA; I-125), and it was demonstrated that aARC stored and secreted ANF 18- and 16-times more, respectively, when compared to vARC, Immuno-electron microscopy confirmed that ANF storing secretory granules were present in both types of cardiomyocytes. Expression of ANF and alpha-sm actin in aARC and vARC responded differently to treatment with either IGF-I or bFGF. In aARC, neither IGF-I nor bFGF had an influence on expression of ANF. In vARC, expression of ANF was down-regulated by IGF-I and upregulated by bFGF with regard to both immunoreactivity and message. In contrast to vARC, expression of alpha-sm actin was not affected by IGF-I in aARC, whereas bFGF produced a strong upregulation similar to that found in vARC. Mitogen-activated protein kinases (MAPK) 42 and 44, though, were equally activated by bFGF and IGF-I in both aARC and vARC. (C) 1997 Academic Press Limited.
引用
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页码:2027 / 2039
页数:13
相关论文
共 48 条
[1]   REGULATION OF ATRIAL-NATRIURETIC-PEPTIDE SECRETION BY ALPHA-1-ADRENERGIC RECEPTORS - THE ROLE OF DIFFERENT 2ND MESSENGER PATHWAYS [J].
AMBLER, SK ;
LEITE, MF .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1994, 26 (03) :391-402
[2]  
BOGOYEVITCH MA, 1994, J BIOL CHEM, V269, P1110
[3]   IMMUNOREACTIVE ATRIAL-NATRIURETIC-FACTOR IS PRESENT IN BOTH ATRIA AND VENTRICLES [J].
CANTIN, M ;
DING, J ;
THIBAULT, G ;
GUTKOWSKA, J ;
SALMI, L ;
GARCIA, R ;
GENEST, J .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1987, 52 (1-2) :105-113
[4]  
CANTIN M, 1988, AM J PATHOL, V130, P552
[5]   REGULATION OF CARDIAC GENE-EXPRESSION DURING MYOCARDIAL GROWTH AND HYPERTROPHY - MOLECULAR STUDIES OF AN ADAPTIVE PHYSIOLOGICAL-RESPONSE [J].
CHIEN, KR ;
KNOWLTON, KU ;
ZHU, H ;
CHIEN, S .
FASEB JOURNAL, 1991, 5 (15) :3037-3046
[6]   ATRIAL PRESSURE, DISTENSION, AND PACING FREQUENCY IN ANP SECRETION IN ISOLATED PERFUSED RABBIT ATRIA [J].
CHO, KW ;
SEUL, KH ;
KIM, SH ;
SEUL, KM ;
KOH, GY .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 260 (01) :R39-R46
[7]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[8]   REGULATION OF HYPERTROPHY AND ATROPHY IN CULTURED ADULT HEART-CELLS [J].
CLARK, WA ;
RUDNICK, SJ ;
LAPRES, JJ ;
ANDERSEN, LC ;
LAPOINTE, MC .
CIRCULATION RESEARCH, 1993, 73 (06) :1163-1176
[9]  
CLAYCOMB WC, 1988, BIOCHEM J, V255, P617
[10]   VENTRICULAR ATRIOPEPTIN - UNMASKING OF MESSENGER-RNA AND PEPTIDE-SYNTHESIS BY HYPERTROPHY OR DEXAMETHASONE [J].
DAY, ML ;
SCHWARTZ, D ;
WIEGAND, RC ;
STOCKMAN, PT ;
BRUNNERT, SR ;
TOLUNAY, HE ;
CURRIE, MG ;
STANDAERT, DG ;
NEEDLEMAN, P .
HYPERTENSION, 1987, 9 (05) :485-491