Hatzfeld M, Franke W W
J Cell Biol. 1985 Nov;101(5 Pt 1):1826-41. doi: 10.1083/jcb.101.5.1826.
Cytokeratins are expressed in different types of epithelial cells in certain combinations of polypeptides of the acidic (type I) and basic (type II) subfamilies, showing "expression pairs." We have examined in vitro the ability of purified and denatured cytokeratin polypeptides of human, bovine, and rat origin to form the characteristic heterotypic subunit complexes, as determined by various electrophoretic techniques and chemical cross-linking, and, subsequently, intermediate-sized filaments (IFs), as shown by electron microscopy. We have found that all of the diverse type I cytokeratin polypeptides examined can form complexes and IFs when allowed to react with equimolar amounts of any of the type II polypeptides. Examples of successful subunit complex and IF formation in vitro include combinations of polypeptides that have never been found to occur in the same cell type in vivo, such as between epidermal cytokeratins and those from simple epithelia, and also heterologous combinations between cytokeratins from different species. The reconstituted complexes and IFs show stability properties, as determined by gradual "melting" and reassociation, that are similar to those of comparable native combinations or characteristic for the specific new pair combination. The results show that cytokeratin complex and IF formation in vitro requires the pairing of one representative of each the type I and type II subfamilies into the heterotypic tetramer but that there is no structural incompatibility between any of the members of the two subfamilies. These findings suggest that the co-expression of specific pair combinations observed in vivo has other reasons than general structural requirements for IF formation and probably rather reflects the selection of certain regulatory programs of expression during cell differentiation. Moreover, the fact that certain cytokeratin polypeptide pairs that readily form complexes in vitro and coexist in the same cells in vivo nevertheless show preferential, if not exclusive, partner relationships in the living cell points to the importance of differences of stabilities among cytokeratin complexes and/or the existence of extracytokeratinous factors involved in the specific formation of certain cytokeratin pairs.
细胞角蛋白以酸性(I型)和碱性(II型)亚家族的特定多肽组合形式在不同类型的上皮细胞中表达,呈现出“表达对”。我们通过各种电泳技术和化学交联,体外检测了人、牛和大鼠来源的纯化变性细胞角蛋白多肽形成特征性异型亚基复合物的能力,随后通过电子显微镜观察了其形成中等大小丝状纤维(IFs)的能力。我们发现,所有检测的不同I型细胞角蛋白多肽在与等摩尔量的任何II型多肽反应时都能形成复合物和IFs。体外成功形成亚基复合物和IFs的例子包括体内从未在同一细胞类型中发现的多肽组合,如表皮细胞角蛋白与简单上皮细胞角蛋白之间的组合,以及不同物种细胞角蛋白之间的异源组合。通过逐步“熔化”和重新缔合测定,重组复合物和IFs显示出与可比天然组合相似或特定新对组合特有的稳定性特性。结果表明,体外细胞角蛋白复合物和IFs的形成需要I型和II型亚家族的各一个代表配对形成异型四聚体,但两个亚家族的任何成员之间不存在结构不相容性。这些发现表明,体内观察到的特定对组合的共表达,其原因并非IF形成的一般结构要求,而可能更反映了细胞分化过程中某些表达调控程序的选择。此外,某些在体外易于形成复合物且在体内同一细胞中共存的细胞角蛋白多肽对,在活细胞中仍显示出优先(如果不是排他性)的伙伴关系,这表明细胞角蛋白复合物之间稳定性差异的重要性和/或存在参与某些细胞角蛋白对特定形成的细胞角蛋白外因子。