Sanger J M, Mittal B, Wegner A, Jockusch B M, Sanger J W
Eur J Cell Biol. 1987 Jun;43(3):421-8.
The actin-severing activity of human platelet gelsolin was analyzed on embryonic skeletal and cardiac myofibrils, and on stress fibers in non-muscle cells. These subcellular structures, although in all three cell types composed of contractile proteins arranged in sarcomeric units, were found to respond differently to gelsolin. The myofibrils in permeabilized myotubes or cardiac cells, as well as in living, microinjected muscle cells proved resistant to a wide concentration range of gelsolin. The same was found for the "mini-sarcomeres" which are seen in developing muscle cells. In contrast, stress fibers in microinjected fibroblasts or epithelial cells, as well as in permeabilized cells, were broken down rapidly by the platelet gelsolin. We conclude from these results that the mini-sarcomeres in embryonic myotubes and cardiac myocytes are not identical with stress fibers.
对人血小板凝溶胶蛋白的肌动蛋白切断活性进行了分析,研究对象包括胚胎骨骼肌和心肌肌原纤维以及非肌肉细胞中的应力纤维。这些亚细胞结构,尽管在所有三种细胞类型中均由排列成肌节单位的收缩蛋白组成,但发现它们对凝溶胶蛋白的反应不同。通透化肌管或心脏细胞中的肌原纤维,以及活的、显微注射的肌肉细胞中的肌原纤维,在凝溶胶蛋白的广泛浓度范围内均表现出抗性。在发育中的肌肉细胞中看到的“微型肌节”也是如此。相比之下,显微注射的成纤维细胞或上皮细胞中的应力纤维,以及通透化细胞中的应力纤维,会被血小板凝溶胶蛋白迅速分解。我们从这些结果得出结论,胚胎肌管和心肌细胞中的微型肌节与应力纤维不同。