Steffen M, Scherdin U, Vértes I, Boecker W, Dietel M, Hölzel F
Department of Internal Medicine, University Hospital Eppendorf, Hamburg.
Genes Chromosomes Cancer. 1992 Jan;4(1):46-57. doi: 10.1002/gcc.2870040107.
The karyotypic and phenotypic stability of cultured rat fibrosarcoma cells was challenged by infection with Moloney murine sarcoma virus (MoMuSV). After transformation, the spindle-like morphology of the parental HH-16 cl.2/1 cells had altered to a rounded phenotype, which was maintained in tumors produced by inoculating transformed cells into congenic animals. In contrast to the parental cells, transformed cells lacked cables of cytokeratins 14-16 and 19 and showed reduction of the mesenchymal marker protein vimentin. Additionally, the morphologically altered cell clones tf-1 to tf-3 had lost growth arrest in the presence of dexamethasone. The DNA of the transformed cells contained between four and six randomly integrated proviral copies. Karyotypic alterations were manifested by reduction of morphologically intact chromosomes in the MoMuSV-transformed cells together with increase of structural aberrations. Three additional markers were identified in the virus-transformed cell clones. Karyotypic instability induced by MoMuSV infection appeared closely related to reduction of the cellular differentiation status, although only cells of clone tf-1 had increased metastatic potential.
莫洛尼氏鼠肉瘤病毒(MoMuSV)感染对培养的大鼠纤维肉瘤细胞的核型和表型稳定性提出了挑战。转化后,亲代HH-16 cl.2/1细胞的纺锤样形态转变为圆形表型,这种表型在将转化细胞接种到同基因动物体内产生的肿瘤中得以维持。与亲代细胞相比,转化细胞缺乏细胞角蛋白14 - 16和19的纤维束,并且间充质标记蛋白波形蛋白减少。此外,形态改变的细胞克隆tf-1至tf-3在存在地塞米松的情况下失去了生长停滞。转化细胞的DNA包含4至6个随机整合的前病毒拷贝。核型改变表现为MoMuSV转化细胞中形态完整染色体数量减少以及结构畸变增加。在病毒转化的细胞克隆中还鉴定出另外三个标记。MoMuSV感染诱导的核型不稳定性似乎与细胞分化状态的降低密切相关,尽管只有克隆tf-1的细胞具有增加的转移潜能。