Rapid transition of cardiac myocytes from hyperplasia to hypertrophy during postnatal development

被引:653
作者
Li, FQ [1 ]
Wang, XJ [1 ]
Capasso, JM [1 ]
Gerdes, AM [1 ]
机构
[1] UNIV S DAKOTA, SCH MED,DEPT ANAT & STRUCT BIOL, VERMILLION, SD 57069 USA
关键词
isolated myocytes; hyperplasia; hypertrophy; postnatal growth;
D O I
10.1006/jmcc.1996.0163
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The switch from myocyte hyperplasia to hypertrophy occurs during the early postnatal period. The exact temporal sequence when cardiac myocytes cease dividing and become terminally differentiated is not certain, although it is currently believed that the transition takes place gradually over a 1-2-week period. The present investigation has characterized the growth pattern of cardiac myocytes during the early postnatal period. Cardiac myocytes were enzymatically isolated from the hearts of 1, 2, 3, 4, 6, 8, 10, and 12-day-old rats for the measurements of binucleation, cell volume and myocyte number. Almost all myocytes were mononucleated and cell volume remained relatively constant during the first 3 days of age. Increases in cell volume and binucleation of myocytes were first detected at day 4. Myocyte volume increased 2.5-fold from day 3 to day 12 (1416 +/- 320 compared to 3533 +/- 339 mu m(3)). The percentage of binucleated myocytes began to increase at day 4 and proceeded at a high rate, reaching the adult level of approximately 90% at day 12. Myocyte number increased 68% during the first 3 days (from 13.6 +/- 3.5 x 10(6) at day 1 to 22.9 +/- 5.6 x 10(10) at day 3) and remained constant thereafter. To confirm that no further myocyte division exists after 4 days, bromodeoxyuridine (Brdu) was administered to 4-day-old rats and the fate of DNA-synthesizing myocytes was examined 2 h and 2, 4, 6 and 8 days after Brdu injection. About 12% of myocytes were labeled with Brdu at 2 h and all were mononucleated at that time. Gradually, these Brdu-labeled myocytes became binucleated. However, the percentage of labeled myocytes in all groups was identical, indicating that DNA-synthesizing myocytes were becoming binucleated without further cell division after 4 days of age. Within 8 days after injection, approximately 82% of total labeled myocytes were binucleated, while the others remained mononucleated. Sarcomeric alpha-actinin was fully disassembled in dividing myocytes of 2-day-old rats, while typical alpha-actinin striations were present in dividing myocytes of 4-day-old rats. The results from this study suggest that a rapid switch from myocyte hyperplasia to hypertrophy occurs between postnatal day 3 and 4 in rats hearts. (C) 1996 Academic Press Limited
引用
收藏
页码:1737 / 1746
页数:10
相关论文
共 39 条
[1]   MORPHOMETRIC STUDY OF EARLY POSTNATAL-DEVELOPMENT IN THE LEFT AND RIGHT VENTRICULAR MYOCARDIUM OF THE RAT .1. HYPERTROPHY, HYPERPLASIA, AND BINUCLEATION OF MYOCYTES [J].
ANVERSA, P ;
OLIVETTI, G ;
LOUD, AV .
CIRCULATION RESEARCH, 1980, 46 (04) :495-502
[2]   POSTNATAL-DEVELOPMENT OF THE M-BAND IN RAT CARDIAC MYOFIBRILS [J].
ANVERSA, P ;
OLIVETTI, G ;
BRACCHI, PG ;
LOUD, AV .
CIRCULATION RESEARCH, 1981, 48 (04) :561-568
[3]   INFLUENCE OF AGE, GROWTH, AND SEX ON CARDIAC MYOCYTE SIZE AND NUMBER IN RATS [J].
BAI, SL ;
CAMPBELL, SE ;
MOORE, JA ;
MORALES, MC ;
GERDES, AM .
ANATOMICAL RECORD, 1990, 226 (02) :207-212
[4]  
BILSEN MV, 1993, CARDIOVASC RES, V27, P1140
[5]  
BUGAISKY L, 1979, TEX REP BIOL MED, V39, P123
[6]   COMPARISON OF REGIONAL DIFFERENCES IN CARDIAC MYOCYTE DIMENSIONS IN RATS, HAMSTERS, AND GUINEA-PIGS [J].
CAMPBELL, SE ;
GERDES, AM ;
SMITH, TD .
ANATOMICAL RECORD, 1987, 219 (01) :53-59
[7]   ANALYSIS OF POPULATION CYTOKINETICS OF CHICK MYOCARDIAL-CELLS IN TISSUE-CULTURE [J].
CLARK, WA ;
FISCHMAN, DA .
DEVELOPMENTAL BIOLOGY, 1983, 97 (01) :1-9
[8]  
CLAYCOMB WC, 1975, J BIOL CHEM, V250, P3229
[9]  
CLUBB FJ, 1987, LAB INVEST, V56, P189
[10]   CARDIOMEGALY DUE TO MYOCYTE HYPERPLASIA IN PERINATAL RATS EXPOSED TO 200 PPM CARBON-MONOXIDE [J].
CLUBB, FJ ;
PENNEY, DG ;
BAYLERIAN, MS ;
BISHOP, SP .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1986, 18 (05) :477-486