Clubb F J, Bishop S P
Lab Invest. 1984 May;50(5):571-7.
The purposes of this study were to characterize myocardial cell growth in neonatal rats and investigate the mechanism of binucleation in myocardial cells. To test the hypothesis that binucleated myocardial cells result from karyokinesis without cytokinesis, experiments were designed to measure the rate of DNA synthesis and the percentage of binucleated myocardial cells in neonatal rats during growth. Estimates of myocardial cell nuclear divisions were obtained from rats pulsed with tritiated thymidine at 17 days of gestation. Autoradiograms were prepared from isolated myocardial cells of rats killed at various ages postpartum, and the number of developed silver halide grains over myocardial cell nuclei was calculated. This estimated the mitotic activity of nuclei. To determine myocardial cell DNA synthesis postpartum, another set of rats were injected at various time periods with 4 hourly doses of tritiated thymidine, and hearts were fixed by perfusion 1 hour later. Labeling index of myocardial cells was calculated (labeled/total myocardial cells) from autoradiograms prepared on 1 micron thick, methacrylate-embedded heart cross-sections. Results of this study indicated that the growth of myocardial cells in the neonatal period can be divided into three phases: (a) a hyperplastic phase, (b) a transitional phase, and (c) a hypertrophic phase. Binucleation of myocardial cells was not due to fusion of mononucleated cells, because there was continued DNA synthesis in the neonatal hearts, reflected by continued incorporation of tritiated thymidine; in addition, the grain counts per nucleus of the binucleated myocardial cells were half that of mononucleated cells; nor was binucleation due to amitotic splitting of single nuclei, since binucleated myocardial cells had similar grain counts over each nucleus. We conclude that the formation of binucleated myocardial cells is an early indicator of growth hypertrophy in the neonatal rat and a result of mitosis without cytokinesis.
本研究的目的是描述新生大鼠心肌细胞的生长特征,并探究心肌细胞双核化的机制。为了验证双核心肌细胞是由核分裂而无胞质分裂导致的这一假设,设计了实验来测量新生大鼠生长过程中DNA合成速率和双核心肌细胞的百分比。从妊娠17天用氚标记胸腺嘧啶脉冲处理的大鼠中获得心肌细胞核分裂的估计值。从产后不同年龄处死的大鼠分离出的心肌细胞制备放射自显影片,并计算心肌细胞核上显影的卤化银颗粒数量。这估计了细胞核的有丝分裂活性。为了确定产后心肌细胞的DNA合成情况,另一组大鼠在不同时间段每隔4小时注射一次氚标记胸腺嘧啶,1小时后通过灌注固定心脏。根据在1微米厚的甲基丙烯酸酯包埋的心脏横切片上制备的放射自显影片计算心肌细胞的标记指数(标记细胞数/总心肌细胞数)。本研究结果表明,新生期心肌细胞的生长可分为三个阶段:(a)增生期,(b)过渡期,(c)肥大期。心肌细胞的双核化不是由于单核细胞的融合,因为新生心脏中存在持续的DNA合成,这通过氚标记胸腺嘧啶的持续掺入得以体现;此外,双核心肌细胞每个核的颗粒计数是单核细胞的一半;双核化也不是由于单核的无丝分裂,因为双核心肌细胞每个核的颗粒计数相似。我们得出结论,双核心肌细胞的形成是新生大鼠生长肥大的早期指标,是有丝分裂而无胞质分裂的结果。