Samuel J L, Bertier B, Bugaisky L, Marotte F, Swynghedauw B, Schwartz K, Rappaport L
Eur J Cell Biol. 1984 Jul;34(2):300-6.
To elucidate the role of the cytoskeleton in the development of adult heart, microtubules and intermediate filaments of desmin were studied in young and adult rat heart myocytes during the onset of growth, after mechanical overloading induced by aortic stenosis. Such overloading is known to cause heart hypertrophy by stimulating overall protein synthesis, and to initiate a shift in myosin isozymes. For this study, we used double immunolabelling of isolated myocytes with specific antibodies raised against tubulin, desmin, and the two main isomyosins V1 and V3. Whereas desmin remained unchanged, tubulin was redistributed in arrays parallel to the long axis of the myocytes, and was densest around the nuclei. Alterations in the microtubule pattern were observed very early after aortic stenosis, during the onset of heart growth; they were transitory, and did not occur simultaneously in all myocytes. Chronological examination of myocytes labelling with both antitubulin and anti V3 myosin clearly suggested that the transitory alteration in the microtubule pattern was an early event preceding the change in the expression of the myosin gene. Results, observed in young rats, in which mitosis is stimulated by overloading, and in adult rats, exhibiting no mitosis, showed that microtubules are involved in the development of cells in which mitosis does not occur. This work provides the first evidence of a correlation in functional adult heart, between the reorganization of cytoplasmic microtubules and the onset of growth.
为阐明细胞骨架在成年心脏发育中的作用,我们在主动脉狭窄诱导的机械性超负荷后,对幼年和成年大鼠心肌细胞生长开始阶段的微管和结蛋白中间丝进行了研究。已知这种超负荷通过刺激整体蛋白质合成导致心脏肥大,并引发肌球蛋白同工酶的转变。在本研究中,我们用针对微管蛋白、结蛋白以及两种主要的同工型肌球蛋白V1和V3的特异性抗体对分离的心肌细胞进行了双重免疫标记。结蛋白保持不变,而微管蛋白重新分布在与心肌细胞长轴平行的阵列中,并且在细胞核周围最为密集。在主动脉狭窄后心脏生长开始的早期就观察到微管模式的改变;这些改变是短暂的,并非在所有心肌细胞中同时发生。用抗微管蛋白和抗V3肌球蛋白对心肌细胞进行标记的时间顺序检查清楚地表明,微管模式的短暂改变是肌球蛋白基因表达变化之前的早期事件。在幼年大鼠(其有丝分裂因超负荷而被刺激)和成年大鼠(无有丝分裂)中观察到的结果表明,微管参与了无有丝分裂细胞的发育。这项工作首次证明了在成年功能性心脏中,细胞质微管的重组与生长开始之间存在相关性。