The intermediate-sized filaments in rat kangaroo PtK2 cells. II. Structure and composition of isolated filaments.

Cytobiologie Pub Date : 1978-08-01
W W Franke, E Schmid, M Osborn, K Weber
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Abstract

When cultured cells of the rat kangaroo cell line PtK2 grown on plastic or glass surfaces are lysed and extracted with combinations of low and high salt buffers and the non-ionic detergent Triton X-100 cytoskeletal preparations are obtained that show an enrichment of 6 to 11 nm thick filaments. The arrays of these filaments have been examined by various light and electron microscopic techniques, including ultrathin sectioning, whole mount transmission electron microscopy, negative staining, and indirect immunofluorescence microscopy. In addition, 6 to 11 nm filaments isolated from these cells with similar extraction procedures and with centrifugation techniques have been examined by electron microscopy. The arrays of these isolated intermediate-sized filaments, their ultrastructure and their specific decoration by certain antibodies present in normal rabbit sera as well as by guinea pig antibodies against purified bovine prekeratin is demonstrated. When preparations enriched in these intermediate-sized filaments are examined by SDS-polyacrylamide gel electrophoresis a corresponding enrichment of three polypeptide bands with apparent molecular weights of about 45 000, 52 000 and 58 000 (the latter component sometimes appears split into two bands) is observed, besides some residual actin and a few high molecular weight bands. The morphology of the isolated filaments, their immunological reaction with antibodies decorating prekeratin-containing structures, and the sizes of their constitutive polypeptides suggest that these filaments are closely related to prekeratin-containing filaments observed in a variety of epithelial cells.

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大鼠袋鼠PtK2细胞的中等大小纤维。2孤立细丝的结构和组成。
将生长在塑料或玻璃表面的大鼠袋鼠细胞系PtK2的培养细胞裂解,并用低盐和高盐缓冲液和非离子洗涤剂组合提取,得到Triton X-100细胞骨架制剂,该制剂显示富集6至11 nm厚的纤维。这些细丝的阵列已经通过各种光学和电子显微镜技术进行了检查,包括超薄切片、全片透射电子显微镜、阴性染色和间接免疫荧光显微镜。此外,用类似的提取程序和离心技术从这些细胞中分离出6至11 nm的细丝,并通过电子显微镜进行了检测。这些分离的中等大小的纤维的阵列,它们的超微结构和它们的特异性装饰存在于正常兔血清中的某些抗体以及纯化牛角蛋白的豚鼠抗体。当用sds -聚丙烯酰胺凝胶电泳检测富含这些中等大小纤维的制剂时,除了一些残留的肌动蛋白和一些高分子量带外,还观察到相应的三条表观分子量约为45000、52000和58000的多肽带(后者有时出现分裂为两条带)的富集。分离的纤维的形态、它们与修饰含预角蛋白结构的抗体的免疫反应以及它们的组成多肽的大小表明,这些纤维与在各种上皮细胞中观察到的含预角蛋白的纤维密切相关。
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