Expression profiling reveals distinct sets of genes altered during induction and regression of cardiac hypertrophy

被引:162
作者
Friddle, CJ
Koga, T
Rubin, EM
Bristow, J
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Lab, Genome Sci Dept, Berkeley, CA 94720 USA
[2] Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94118 USA
关键词
D O I
10.1073/pnas.100127897
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Although cardiac hypertrophy has been the subject of intensive investigation, regression of hypertrophy has been significantly less studied, precluding large-scale analysis of the relationship between these processes. In the present study, using pharmacological models of cardiac hypertrophy in mice, expression profiling was performed with fragments of more than 4,000 genes to characterize and contrast expression changes during induction and regression of hypertrophy. Administration of angiotensin II and isoproterenol by osmotic minipump produced increases in heart weight (15 and 45%, respectively) that returned to preinduction size after drug withdrawal. From multiple expression analyses of left ventricular RNA isolated at daily time-points during cardiac hypertrophy and regression, we identified sets of genes whose expression was altered at specific stages of this process. While confirming the participation of 25 genes or pathways previously shown to be altered by hypertrophy, a larger set of 30 genes was identified whose expression had not previously been associated with cardiac: hypertrophy or regression. Of the 55 genes that showed reproducible changes during the time course of induction and regression. 32 genes were altered only during induction, and 8 were altered only during regression. This study identified both known and novel genes whose expression is affected at different stages of cardiac hypertrophy and regression and demonstrates that cardiac remodeling during regression utilizes a set of genes that are distinct from those used during induction of hypertrophy.
引用
收藏
页码:6745 / 6750
页数:6
相关论文
共 46 条
[1]  
Agabiti-Rosei E, 1997, ADV EXP MED BIOL, V432, P199
[2]   Fatty acid utilization in the hypertrophied and failing heart: Molecular regulatory mechanisms [J].
Barger, PM ;
Kelly, DP .
AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 1999, 318 (01) :36-42
[3]   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
[4]   MYOSIN HEAVY-CHAIN MESSENGER-RNA DURING THE DEVELOPMENT AND REGRESSION OF MYOCARDIAL HYPERTROPHY [J].
CUTILLETTA, AF .
EUROPEAN HEART JOURNAL, 1984, 5 :193-197
[5]  
DeRisi J, 1996, NAT GENET, V14, P457
[6]   Exploring the metabolic and genetic control of gene expression on a genomic scale [J].
DeRisi, JL ;
Iyer, VR ;
Brown, PO .
SCIENCE, 1997, 278 (5338) :680-686
[7]   Cluster analysis and display of genome-wide expression patterns [J].
Eisen, MB ;
Spellman, PT ;
Brown, PO ;
Botstein, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14863-14868
[8]  
Eisen MB, 1999, METHOD ENZYMOL, V303, P179
[9]   Immediate postnatal rat heart development modified by abdominal aortic banding: Analysis of gene expression [J].
Engelmann, GL ;
Campbell, SE ;
Rakusan, K .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1996, 164 :47-56
[10]   ANGIOTENSIN-II INDUCES PLASMINOGEN-ACTIVATOR INHIBITOR-1 AND INHIBITOR-2 EXPRESSION IN VASCULAR ENDOTHELIAL AND SMOOTH-MUSCLE CELLS [J].
FEENER, EP ;
NORTHRUP, JM ;
AIELLO, LP ;
KING, GL .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (03) :1353-1362