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若丹明-肌动蛋白在心肌细胞中的掺入模式和时间进程。

Pattern and time course of rhodamine-actin incorporation in cardiac myocytes.

作者信息

Glacy S D

出版信息

J Cell Biol. 1983 Apr;96(4):1164-7. doi: 10.1083/jcb.96.4.1164.

Abstract

Microinjection of skeletal actin labeled with rhodamine into cultured cardiac myocytes was followed by rapid incorporation of fluorescence into myofibrils of the cells. Myocytes examined as shortly as 5 min postinjection displayed fluorescent bands corresponding to the sarcomeres. By 10 min, distinct alternating wide and narrow bands of fluorescence were observed. The wide bands appeared to correspond to the full breadth of the I-bands, whereas the narrow bands of fluorescence corresponded to the M-lines. This pattern of fluorescence remained essentially unchanged for at least 15 h postinjection. The myofibrils of cardiac myocytes were functional after rhodamine-actin incorporation as judged by their ability to contract. The results of this study suggest that cardiac myofibrils are morphologically stable structures which, nonetheless, exhibit extensive exchange of actin subunits.

摘要

将用罗丹明标记的骨骼肌肌动蛋白显微注射到培养的心肌细胞中后,荧光迅速掺入细胞的肌原纤维中。注射后短至5分钟检查的心肌细胞显示出与肌节相对应的荧光带。到10分钟时,观察到明显交替的宽荧光带和窄荧光带。宽荧光带似乎对应于I带的全宽,而窄荧光带对应于M线。这种荧光模式在注射后至少15小时基本保持不变。根据其收缩能力判断,罗丹明-肌动蛋白掺入后心肌细胞的肌原纤维具有功能。这项研究的结果表明,心肌肌原纤维是形态稳定的结构,尽管如此,它们仍表现出肌动蛋白亚基的广泛交换。

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