Limas C J
Am J Physiol. 1980 Jan;238(1):H66-72. doi: 10.1152/ajpheart.1980.238.1.H66.
In vitro DNA synthesis by isolated myocardial nuclei declines rapidly during postnatal growth. To study the mechanism(s) responsible for this decline, cytoplasmic extracts (CE) were prepared from isolated rat myocytes at different times after birth. CE from 2-day-old rats stimulated in vitro DNA synthesis by myocardial nuclei from adult (6 mo old) rats (55 +/- 6 pmol[3H]dTMP . mg DNA-1 . 15 min-1 vs. 32 +/- 4 pmol [3H]dTMP . mg DNA-1 . 15 min-1 in untreated controls, P less than 0.01). The ability of cytoplasmic extracts of stimulate DNA synthesis decreased with age, from 73 +/- 9% over controls at age 2 days to 18 +/- 6 at 28 days; adult myocytes were essentially ineffective. Pulse-chase experiments demonstrated that CE-directed DNA synthesis was replicative and discontinuous. CE stimulatory activity was heat-labile, nondialyzable, trypsin-sensitive, and distinct from DNA polymerases. The results indicate that a) adult myocyte nuclei can be induced to synthesize DNA by cytoplasmic extracts from neonatal rats, and b) that absence of regulatory cytoplasmic factor(s) may, in part, explain the age-dependent decline in myocardial DNA synthesis.
出生后生长过程中,分离的心肌细胞核的体外DNA合成迅速下降。为了研究导致这种下降的机制,在出生后不同时间从分离的大鼠心肌细胞制备细胞质提取物(CE)。2日龄大鼠的CE刺激成年(6月龄)大鼠心肌细胞核的体外DNA合成(55±6 pmol[3H]dTMP·mg DNA-1·15 min-1,而未处理对照为32±4 pmol[3H]dTMP·mg DNA-1·15 min-1,P<0.01)。刺激DNA合成的细胞质提取物的能力随年龄下降,从2日龄时比对照高73±9%降至28日龄时的18±6;成年心肌细胞基本无效。脉冲追踪实验表明,CE指导的DNA合成是复制性的且是不连续的。CE刺激活性对热不稳定、不可透析、对胰蛋白酶敏感,且与DNA聚合酶不同。结果表明:a)成年心肌细胞核可被新生大鼠的细胞质提取物诱导合成DNA;b)缺乏调节性细胞质因子可能部分解释了心肌DNA合成随年龄的下降。