COORDINATED EFFECTS OF INSULIN-LIKE GROWTH-FACTOR-I ON INHIBITORY PATHWAYS OF CELL-CYCLE PROGRESSION IN CULTURED CARDIAC-MUSCLE-CELLS

被引:15
作者
CHEN, WH
PELLEGATA, NS
WANG, PH
机构
[1] UNIV CALIF IRVINE, DEPT MED, IRVINE, CA 92717 USA
[2] UNIV CALIF IRVINE, DEPT MICROBIOL & MOLEC GENET, IRVINE, CA 92717 USA
[3] UNIV CALIF IRVINE, DEPT BIOL CHEM, IRVINE, CA 92717 USA
关键词
D O I
10.1210/en.136.11.5240
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Insulin-like growth factor I (IGF I) plays a key role in the regulation of cell proliferation. Progression of the cell cycle is regulated by stimulatory and inhibitory pathways. In order to understand the mechanisms through which IGF I regulates cardiac muscle growth, we have studied the effects of IGF I on inhibitory pathways involving p53 and WAF1 in cultured cardiac muscle cell line H9C2. The onset of DNA synthesis in response to IGF I stimulation was preceded by activation of p53 expression. In addition, IGF I increased p53-dependent and p53-independent induction of WAF1 in H9C2 cells. Dose-response studies showed that IGF I effects on p53-dependent and p53-independent induction of WAF1 occur at physiological concentrations of IGF I. These data indicate that IGF I coordinately regulates inhibitory pathways of cell cycle progression, and that p53-dependent and p53-independent induction of WAF1 may provide negative control mechanisms to regulate stimulatory pathways of cell cycle progression activated by IGF I.
引用
收藏
页码:5240 / 5243
页数:4
相关论文
共 25 条
[1]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[2]  
CONDORELLI G, 1994, J BIOL CHEM, V269, P8510
[3]   INDUCTION OF MYOCARDIAL INSULIN-LIKE GROWTH FACTOR-I GENE-EXPRESSION IN LEFT-VENTRICULAR HYPERTROPHY [J].
DONOHUE, TJ ;
DWORKIN, LD ;
LANGO, MN ;
FLIEGNER, K ;
LANGO, RP ;
BENSTEIN, JA ;
SLATER, WR ;
CATANESE, VM .
CIRCULATION, 1994, 89 (02) :799-809
[4]   WAF1, A POTENTIAL MEDIATOR OF P53 TUMOR SUPPRESSION [J].
ELDEIRY, WS ;
TOKINO, T ;
VELCULESCU, VE ;
LEVY, DB ;
PARSONS, R ;
TRENT, JM ;
LIN, D ;
MERCER, WE ;
KINZLER, KW ;
VOGELSTEIN, B .
CELL, 1993, 75 (04) :817-825
[5]   INSULIN-LIKE GROWTH-FACTORS AND NEONATAL CARDIOMYOCYTE DEVELOPMENT - VENTRICULAR GENE-EXPRESSION AND MEMBRANE-RECEPTOR VARIATIONS IN NORMOTENSIVE AND HYPERTENSIVE RATS [J].
ENGELMANN, GL ;
BOEHM, KD ;
HASKELL, JF ;
KHAIRALLAH, PA ;
ILAN, J .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1989, 63 (1-2) :1-14
[6]   WILD-TYPE P53 CAN DOWN-MODULATE THE ACTIVITY OF VARIOUS PROMOTERS [J].
GINSBERG, D ;
MECHTA, F ;
YANIV, M ;
OREN, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (22) :9979-9983
[7]  
GULLER H, 1988, P NATL ACAD SCI USA, V85, P4889
[8]   CORRELATION OF TERMINAL CELL-CYCLE ARREST OF SKELETAL-MUSCLE WITH INDUCTION OF P21 BY MYOD [J].
HALEVY, O ;
NOVITCH, BG ;
SPICER, DB ;
SKAPEK, SX ;
RHEE, J ;
HANNON, GJ ;
BEACH, D ;
LASSAR, AB .
SCIENCE, 1995, 267 (5200) :1018-1021
[9]  
HARPER JW, 1993, CELL, V75, P805
[10]   MORPHOLOGICAL, BIOCHEMICAL, AND ELECTROPHYSIOLOGICAL CHARACTERIZATION OF A CLONAL CELL (H9C2) LINE FROM RAT-HEART [J].
HESCHELER, J ;
MEYER, R ;
PLANT, S ;
KRAUTWURST, D ;
ROSENTHAL, W ;
SCHULTZ, G .
CIRCULATION RESEARCH, 1991, 69 (06) :1476-1486