Changes in collagenase and collagen gene expression after induction of aortocaval fistula in rats

被引:30
作者
Dolgilevich, SM
Siri, FM
Atlas, SA
Eng, C
机构
[1] Vet Affairs Med Ctr, Cardiac Res Lab, Bronx, NY 10468 USA
[2] Vet Affairs Med Ctr, Hypertens Res Lab, Bronx, NY 10468 USA
[3] Mt Sinai Sch Med, Dept Med, Bronx, NY 10468 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2001年 / 281卷 / 01期
关键词
hypertrophy; metalloproteinases; molecular biology; myocardium;
D O I
10.1152/ajpheart.2001.281.1.H207
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Progressive ventricular dilatation commonly accompanies the transition to overt failure in chronically overloaded hearts; however, only recently have studies begun to elucidate underlying molecular alterations. In particular, the potential role of altered myocardial expression of the procollagenase gene in this process has not previously been examined. Biventricular hypertrophy and dilatation were produced in rats by creating an abdominal aortocaval fistula. The time courses of changes in expression of collagen I and III genes and of the procollagenase gene (matrix metalloproteinase-1, MMP-1) were assessed by Northern blot hybridization. Expression of all three genes increased promptly; however, collagenase gene expression peaked much earlier (8 h) than did expression of either of the collagen genes (7 days), and all returned to baseline levels by 45 days. These data corroborate earlier reports of increased collagen gene expression in this model, but more importantly, they provide the first evidence of concurrent activation of collagenase gene expression, suggesting that enhancement of collagen degradation may be a prerequisite for structural cardiac dilatation.
引用
收藏
页码:H207 / H214
页数:8
相关论文
共 34 条
[1]   STRUCTURE OF A CDNA FOR THE PRO-ALPHA2 CHAIN OF HUMAN TYPE-I PROCOLLAGEN - COMPARISON WITH CHICK CDNA FOR PROALPHA2(I) IDENTIFIES STRUCTURALLY CONSERVED FEATURES OF THE PROTEIN AND THE GENE [J].
BERNARD, MP ;
MYERS, JC ;
CHU, ML ;
RAMIREZ, F ;
EIKENBERRY, EF ;
PROCKOP, DJ .
BIOCHEMISTRY, 1983, 22 (05) :1139-1145
[2]   REGULATION OF FIBRILLAR COLLAGEN TYPE-I AND TYPE-III AND BASEMENT-MEMBRANE TYPE-IV COLLAGEN GENE-EXPRESSION IN PRESSURE OVERLOADED RAT MYOCARDIUM [J].
CHAPMAN, D ;
WEBER, KT ;
EGHBALI, M .
CIRCULATION RESEARCH, 1990, 67 (04) :787-794
[3]   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
[4]  
CHU ML, 1985, J BIOL CHEM, V260, P4357
[5]   EFFECT OF GROWTH-FACTORS ON COLLAGEN-METABOLISM IN CULTURED HUMAN HEART FIBROBLASTS [J].
CHUA, CC ;
CHUA, BHL ;
ZHAO, ZY ;
KREBS, C ;
DIGLIO, C ;
PERRIN, E .
CONNECTIVE TISSUE RESEARCH, 1991, 26 (04) :271-281
[6]   REGULATION OF COLLAGEN DEGRADATION IN THE RAT MYOCARDIUM AFTER INFARCTION [J].
CLEUTJENS, JPM ;
KANDALA, JC ;
GUARDA, E ;
GUNTAKA, RV ;
WEBER, KT .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1995, 27 (06) :1281-1292
[7]   CHARACTERIZATION OF ANGIOTENSIN-II RECEPTORS IN CULTURED ADULT-RAT CARDIAC FIBROBLASTS - COUPLING TO SIGNALING SYSTEMS AND GENE-EXPRESSION [J].
CRABOS, M ;
ROTH, M ;
HAHN, AWA ;
ERNE, P .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (06) :2372-2378
[8]   CONGESTIVE-HEART-FAILURE IN PATIENTS WITH VALVULAR AORTIC-STENOSIS - A CLINICAL AND ECHOCARDIOGRAPHIC DOPPLER STUDY [J].
FAGGIANO, P ;
RUSCONI, C ;
SABATINI, T ;
GHIZZONI, G ;
SORGATO, A ;
GARDINI, A .
CARDIOLOGY, 1995, 86 (02) :120-129
[9]   Endothelin-1 and angiotensin II receptors in cells from rat hypertrophied heart - Receptor regulation and intracellular Ca2+ modulation [J].
Fareh, J ;
Touyz, RM ;
Schiffrin, EL ;
Thibault, G .
CIRCULATION RESEARCH, 1996, 78 (02) :302-311
[10]   HEART SIZE [J].
FORD, LE .
CIRCULATION RESEARCH, 1976, 39 (03) :297-303