Schmid E, Schiller D L, Grund C, Stadler J, Franke W W
J Cell Biol. 1983 Jan;96(1):37-50. doi: 10.1083/jcb.96.1.37.
Different clonal cell lines have been isolated from cultures of mammary gland epithelium of lactating cow's udder and have been grown in culture media containing high concentrations of hydrocortisone, insulin, and prolactin. These cell (BMGE+H), which grow in monolayers of typical epithelial appearance, are not tightly packed, but leave intercellular spaces spanned by desmosomal bridges. The cells contain extended arrays of cytokeratin fibrils, arranged in bundles attached to desmosomes. Gel electophoresis show that they synthesize cytokeratins similar, if not identical, to those found in bovine epidermis and udder, including two large (mol wt 58,500 and 59,000) and basic (pH range: 7-8) and two small (mol wt 45,500 and 50,000) and acidic (pH 5.32 and 5.36) components that also occur in phosphorylated forms. Two further cytokeratins of mol wts 44,000 (approximately pH 5.7) and 53,000 (pH 6.3) are detected as minor cytokeratins in some cell clones. BMGE+H cells do not produce vimentin filaments as determined by immunofluorescence microscopy and gel electrophoresis. By contrast, BMGE-H cells, which have emerged from the same original culture but have been grown without hormones added, are not only morphologically different, but also contain vimentin filaments and a different set of cytokeratins, the most striking difference being the absence of the two acidic cytokeratins of mol wt 50,000 and 45,500. Cells of the BMGE+H line are characterized by an unusual epithelial morphology and represent the first example of a nonmalignant permanent cell line in vitro that produces cytokeratin but not vimentin filaments. The results show that (a) tissue-specific patterns of intermediate filament expression can be maintained in permanent epithelial cell lines in culture, at least under certain growth conditions; (b) loss of expression of relatively large, basic cytokeratins is not an inevitable consequence of growth of epithelial cells in vitro. Our results further show that, during culturing, different cell clones with different cytoskeletal composition can emerge from the same cell population and suggest that the presence of certain hormones may have an influence on the expression of intermediate filament proteins.
已从泌乳期奶牛乳腺上皮培养物中分离出不同的克隆细胞系,并在含有高浓度氢化可的松、胰岛素和催乳素的培养基中培养。这些细胞(BMGE+H)以典型上皮外观的单层形式生长,细胞排列并不紧密,细胞间由桥粒连接。细胞含有延伸的细胞角蛋白原纤维阵列,排列成束并附着于桥粒。凝胶电泳显示,它们合成的细胞角蛋白与牛表皮和乳腺中发现的细胞角蛋白相似(即便不完全相同),包括两种大分子(分子量58,500和59,000)且呈碱性(pH范围:7 - 8)的以及两种小分子(分子量45,500和50,000)且呈酸性(pH 5.32和5.36)的成分,这些成分也以磷酸化形式存在。在一些细胞克隆中还检测到另外两种分子量分别为44,000(约pH 5.7)和53,000(pH 6.3)的细胞角蛋白,为次要成分。通过免疫荧光显微镜和凝胶电泳测定,BMGE+H细胞不产生波形蛋白丝。相比之下,源自同一原始培养物但在无激素添加条件下生长的BMGE - H细胞,不仅形态不同,还含有波形蛋白丝和一组不同的细胞角蛋白,最显著的差异是缺少分子量为50,000和45,500的两种酸性细胞角蛋白。BMGE+H系细胞具有独特的上皮形态特征,是体外非恶性永久细胞系中首个产生细胞角蛋白但不产生波形蛋白丝的例子。结果表明:(a)至少在某些生长条件下,中间丝表达的组织特异性模式可在培养的永久上皮细胞系中得以维持;(b)相对大分子碱性细胞角蛋白表达的缺失并非上皮细胞体外生长的必然结果。我们的结果还进一步表明,在培养过程中,同一细胞群体可产生具有不同细胞骨架组成的不同细胞克隆,提示某些激素的存在可能对中间丝蛋白的表达有影响。