Klymkowsky M W, Miller R H, Lane E B
J Cell Biol. 1983 Feb;96(2):494-509. doi: 10.1083/jcb.96.2.494.
The organization of intermediate filaments in cultured epithelial cells was rapidly and radically affected by intracellularly injected monoclonal antikeratin filament antibodies. Different antibodies had different effects, ranging from an apparent splaying apart of keratin filament bundles to the complete disruption of the keratin filament network. Antibodies were detectable within cells for more than four days after injection. The antibody-induced disruption of keratin filament organization had no light-microscopically discernible effect on microfilament or microtubule organization, cellular morphology, mitosis, the integrity of epithelial sheets, mitotic rate, or cellular reintegration after mitosis. Cell-to-cell adhesion junctions survived keratin filament disruption. However, antibody injected into a keratinocyte-derived cell line, rich in desmosomes, brought on a superfasciculation of keratin filament bundles, which appeared to pull desmosomal junctions together, suggesting that desmosomes can move in the plane of the plasma membrane and may only be 'fixed' by their anchoring to the cytoplasmic filament network. Our observations suggest that keratin filaments are not involved in the establishment or maintenance of cell shape in cultured cells.
细胞内注射单克隆抗角蛋白丝抗体后,培养的上皮细胞中间丝的组织会迅速且彻底地受到影响。不同的抗体有不同的作用,从明显使角蛋白丝束散开,到完全破坏角蛋白丝网络。注射后四天多的时间里,细胞内都能检测到抗体。抗体诱导的角蛋白丝组织破坏在光学显微镜下对角丝、微管组织、细胞形态、有丝分裂、上皮片层的完整性、有丝分裂速率或有丝分裂后细胞重新整合均无明显影响。细胞间黏附连接在角蛋白丝破坏后依然存在。然而,将抗体注射到富含桥粒的角质形成细胞系中,会导致角蛋白丝束超成束,这似乎会将桥粒连接拉到一起,表明桥粒可以在质膜平面内移动,可能仅通过其与细胞质丝网络的锚定而“固定”。我们的观察结果表明,角蛋白丝不参与培养细胞中细胞形状的建立或维持。