Paramio J M, Jorcano J L
Department of Cell and Molecular Biology, CIEMAT, Madrid, Spain.
Exp Cell Res. 1994 Dec;215(2):319-31. doi: 10.1006/excr.1994.1348.
Keratins K1 and K10 are early markers of keratinization. Their expression starts when basal keratinocytes are committed to differentiate. To study keratin stability and intermediate filament (IF) assembly and dynamics, we have forced the expression of K1/K10 in epithelial and nonepithelial cell lines. It was observed that these keratins are unable to generate a normal cytoskeleton in fibroblasts, where they form, at most, abnormally short and twisted filaments. However, when transfected into epithelial cells they frequently cointegrate with the endogenous keratin into a well-developed cytoskeleton. These results suggest that the K1/K10 pair is unable to form a keratin network on its own and that, mimicking the in vivo situation, requires a preexisting cytoskeleton. Besides, filaments, transfected K1/K10 also form fairly stable, regularly sized round aggregates with no evidence of organization into IF. Transfections with single genes demonstrated that these structures were generated by K10 alone. These aggregates interacted with most components of the cellular cytoskeleton, altering the distribution of the endogenous keratins, actin, vimentin, and tubulin. Kinetic experiments in transfected PtK2 cells showed that, contrary to expectations, K10 does not integrate directly into the preexisting cytoskeleton, but assembles into the stable nonfilamentous aggregates. From these structures, K10 evolves toward the formation of IF together with the endogenous keratins through a complex and highly dynamic process, which involves substantial rearrangement of the endogenous keratin cytoskeleton. These results demonstrate that K1 and K10 have properties different from those described for other keratins and that epithelial IF are surprisingly dynamic structures.
角蛋白K1和K10是角质化的早期标志物。它们的表达在基底角质形成细胞开始分化时启动。为了研究角蛋白稳定性以及中间丝(IF)的组装和动力学,我们在上皮和非上皮细胞系中强制表达K1/K10。据观察,这些角蛋白在成纤维细胞中无法生成正常的细胞骨架,在成纤维细胞中它们最多形成异常短且扭曲的细丝。然而,当转染到上皮细胞中时,它们经常与内源性角蛋白共同整合到发育良好的细胞骨架中。这些结果表明,K1/K10对自身无法形成角蛋白网络,并且模仿体内情况时,需要预先存在的细胞骨架。此外,转染的K1/K10细丝还形成相当稳定、大小规则的圆形聚集体,没有组织成中间丝的迹象。单基因转染表明这些结构仅由K10产生。这些聚集体与细胞骨架的大多数成分相互作用,改变了内源性角蛋白、肌动蛋白、波形蛋白和微管蛋白的分布。在转染的PtK2细胞中进行的动力学实验表明,与预期相反,K10并不直接整合到预先存在的细胞骨架中,而是组装成稳定的非丝状聚集体。从这些结构开始,K10通过一个复杂且高度动态的过程与内源性角蛋白一起向中间丝的形成演变,这涉及内源性角蛋白细胞骨架的大量重排。这些结果表明,K1和K10具有与其他角蛋白不同的特性,并且上皮中间丝是令人惊讶的动态结构。