期刊论文详细信息
Cell Structure and Function
Establishment and Characterization of a SV40 T-Antigen Immortalized Epithelial-Like Cell Line Derived from the Newborn Rat Colorectum and Its Malignant Transformation by the ras Oncogene
Ken Seshimo2  Masaharu Mori3  Masahiro Miyazaki2  Kunzo Orita1  Masayoshi Namba2 
[1] First Department of Surgery, Okayama University Medical School;Department of Cell Biology, Institute of Molecular and Cellular Biology;First Department of Pathology, Okayama University Medical School
关键词: rat colorectal epithelial-like cells;    immortalization;    SV40 T-antigen;    cloned activated c-Ha-ras oncogene;    malignant transformation;   
DOI  :  10.1247/csf.18.345
学科分类:分子生物学,细胞生物学和基因
来源: Japan Society for Cell Biology
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【 摘 要 】

References(38)Cited-By(2)Epithelial-like cells from the colorectum of one-day-old newborn rats were immortalized by transfection with the simian virus 40 (SV40) T-antigen gene, and a cell line OUMS-25 was established. The cells were positive for the SV40 T-antigen, and immunoreactive to a colonic epithelial cell monoclonal antibody and a keratin-18 monoclonal antibody. Ultrastructural studies revealed the presence of microvilli on the cell surface and desmosomes between the adjacent cells. Karyotypic analysis showed that OUMS-25 cells were aneuploid. Cloning efficiency of the cells was 0.01% in soft agar. However, the cells were not tumorigenic in the syngeneic newborn rats. The cells were further transformed by transfection with the cloned activated c-Ha-ras oncogene containing a point mutation within codon 61. Characteristics of the activated-c-Ha-ras transfected cells (OUMS-25/RAS) were different in some respects from those of the parent cells (OUMS-25). OUMS-25/RAS cells demonstrated more malignant morphology, elevated cloning efficiency in soft agar, and tumorigenicity. This is the first report on the immortalization and malignant transformation of colorectal epithelial-like cells by transfection with a combination of SV40 T-antigen gene and cloned activated c-Ha-ras- oncogene.

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