Regauer S, Franke W W, Virtanen I
J Cell Biol. 1985 Apr;100(4):997-1009. doi: 10.1083/jcb.100.4.997.
Using immunofluorescence microscopy and two-dimensional gel electrophoresis, we compared the cytoskeletal proteins expressed by human amnion epithelium in situ, obtained from pregnancies of from 10-wk to birth, with the corresponding proteins from cultured amnion epithelial cells and cultures of cells from the amniotic fluid of 16 week pregnancies. Epithelia of week 16 fetuses already display tissue-specific patterns of cytokeratin polypeptides which are similar, although not identical, to those of the corresponding adult tissues. In the case of the simple amnion epithelium, a complex and characteristic complement of cytokeratin polypeptides of Mr 58,000 (No. 5), 56,000 (No. 6), 54,000 (No. 7), 52,500 (No. 8), 50,000 (No. 14), 46,000 (No. 17), 45,000 (No. 18), and 40,000 (No. 19) is present by week 10 of pregnancy and is essentially maintained until birth, with the addition of cytokeratin No. 4 (Mr 59,000) and the disappearance of No. 7 (Mr 54,000) at week 16 of pregnancy. In full-term placentae, the amnion epithelium displays two morphologically distinct regions, i.e., a simple and a stratified epithelium, both of which express the typical amnion cytokeratin polypeptides. However, in addition the stratified epithelium also synthesizes large amounts of special epidermal cytokeratins such as No. 1 (Mr 68,000), 10 (Mr 56,500), and 11 (Mr 56,000). In culture amnion epithelial cells obtained from either 16-wk pregnancies or full-term placentae will continue to synthesize the amnion-typical cytokeratin pattern, except for a loss of detection of component No. 4. This pattern is considerably different from the cytokeratins synthesized by cultures of cells from amniotic fluids (cytokeratins No. 7, 8, 18, and 19, sometimes with trace amounts of No. 17) and from several so-called "amnion epithelial cell lines." In addition, amnion epithelial cells in situ as well as amnion epithelial cell cultures appear to be heterogeneous in that they possess some cells that co-express cytokeratins and vimentin. These observations lead to several important conclusions: In contrast to the general concept of recent literature, positively charged cytokeratins of the group No. 4-6 can be synthesized in a simple, i.e., one-layered epithelium. The change from simple to stratified amnion epithelium does not require a cessation of synthesis of cytokeratins of the simple epithelium type, but in this case keratins characteristic of the terminally differentiated epidermis (No. 1, 10, and 11) are also synthesized.(ABSTRACT TRUNCATED AT 400 WORDS)
利用免疫荧光显微镜和二维凝胶电泳技术,我们比较了从妊娠10周直至出生的人羊膜上皮原位表达的细胞骨架蛋白,以及培养的羊膜上皮细胞和妊娠16周羊水细胞培养物中的相应蛋白。16周胎儿的上皮细胞已呈现出细胞角蛋白多肽的组织特异性模式,与相应成人组织的模式相似但不完全相同。对于单层羊膜上皮而言,在妊娠10周时就存在一组复杂且具有特征性的细胞角蛋白多肽,其分子量分别为58,000(第5号)、56,000(第6号)、54,000(第7号)、52,500(第8号)、50,000(第14号)、46,000(第17号)、45,000(第18号)和40,000(第19号),并基本维持至出生,不过在妊娠16周时会新增第4号细胞角蛋白(分子量59,000),同时第7号细胞角蛋白(分子量54,000)消失。在足月胎盘中,羊膜上皮呈现出两个形态上不同的区域,即单层上皮和复层上皮,二者均表达典型的羊膜细胞角蛋白多肽。然而,此外复层上皮还会大量合成特殊的表皮细胞角蛋白,如第1号(分子量68,000)、第10号(分子量56,500)和第11号(分子量56,000)。从妊娠16周或足月胎盘获取的培养羊膜上皮细胞会继续合成羊膜典型的细胞角蛋白模式,但第4号成分检测不到。这种模式与羊水细胞培养物(第7、8、18和19号细胞角蛋白,有时还有微量的第17号)以及几种所谓的“羊膜上皮细胞系”合成的细胞角蛋白有很大差异。此外,原位羊膜上皮细胞以及羊膜上皮细胞培养物似乎具有异质性,因为它们含有一些同时表达细胞角蛋白和波形蛋白的细胞。这些观察结果得出了几个重要结论:与近期文献的普遍概念相反,第4 - 6组带正电荷的细胞角蛋白可以在单层上皮中合成。从单层羊膜上皮向复层羊膜上皮的转变并不需要停止合成单层上皮类型的细胞角蛋白,而是在这种情况下还会合成终末分化表皮特有的角蛋白(第1、10和11号)。(摘要截选至400字)