Steinberg M L, Defendi V
J Cell Physiol. 1985 Apr;123(1):117-25. doi: 10.1002/jcp.1041230117.
Transformation of human epidermal keratinocytes by the oncogenic virus SV40 is a stage-specific process in which normal patterns of differentiation are progressively altered over time following infection. Within the context of this scheme, we examined the keratins produced by the infected cells. Immunofluorescence studies indicated that viral infection led to the formation of variant cells visibly lacking the normal keratin cytoskeleton after about 10-15 serial passages (60-90 cell generations) post infection. Analyses of variant cell formation in clonal populations grown on palladium islands revealed that the variants were derived within 2-3 cell divisions from cells containing an apparently normal keratin cytoskeleton, but that variant formation depended upon cell density. Immunoprecipitation of 35S-methionine labelled keratins from the infected keratinocytes revealed a gradual loss of the normal 46, 50, 56 and 58Kd keratin species over a period of many months after infection. The loss of the normal keratins was accompanied by the appearance of at least two species in the 48-52Kd size range not present in uninfected cells and the enhancement of a third, 40Kd, protein quite early after infection. Analysis of the altered keratin patterns on two-dimensional acrylamide gels using either isoelectric focusing (IEF) or non-equilibrium pH gradient electrophoresis (NEPHG) along the first dimension showed that the infected cells produced basic keratins which increased in relative abundance as cells became more transformed with serial passage including at least five isoelectric forms not seen in uninfected cells. Translation of poly A+ RNAs from the infected cells indicated that the altered keratin synthesis probably reflects changes in the translatable mRNA pool.
致癌病毒SV40对人表皮角质形成细胞的转化是一个阶段特异性过程,在此过程中,感染后随着时间推移,正常的分化模式会逐渐改变。在这个方案的背景下,我们检查了被感染细胞产生的角蛋白。免疫荧光研究表明,病毒感染导致在感染后约10 - 15次连续传代(60 - 90个细胞世代)后,形成明显缺乏正常角蛋白细胞骨架的变异细胞。对在钯岛上生长的克隆群体中变异细胞形成的分析表明,这些变异细胞是在2 - 3次细胞分裂内从含有明显正常角蛋白细胞骨架的细胞中产生的,但变异细胞的形成取决于细胞密度。对感染的角质形成细胞中35S - 甲硫氨酸标记的角蛋白进行免疫沉淀显示,感染后经过数月,正常的46、50、56和58Kd角蛋白种类逐渐丢失。正常角蛋白的丢失伴随着至少两种48 - 52Kd大小范围内未感染细胞中不存在的角蛋白种类的出现,以及在感染后相当早的时候第三种40Kd蛋白的增加。使用等电聚焦(IEF)或沿第一维的非平衡pH梯度电泳(NEPHG)在二维丙烯酰胺凝胶上分析改变的角蛋白模式表明,被感染细胞产生碱性角蛋白,随着细胞通过连续传代变得更具转化性,其相对丰度增加,包括至少五种未感染细胞中未见的等电形式。对来自感染细胞的多聚A + RNA的翻译表明,改变的角蛋白合成可能反映了可翻译mRNA库的变化。