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  • Cell & Developmental Biology  (3)
  • 1
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The host-virus interactions of Simian virus 40 (SV40) and polyoma virus (Py) with cell lines established from a teratocarcinoma were studied. The cells utilized in this study were the multipotential stem cell of the teratocarcinoma, embryonal carcinoma, and differentiated cells derived from embryonal carcinoma. Several lines of differentiated cells were established in vitro which included parietal yolk sac, epithelial, and spindle cell types. Embryonal carcinoma cells are not susceptible to infection by either SV40 or Py virus. However, differentiated cells are susceptible to infection by these viruses. The differentiated cells are permissive for Py virus replication and nonpermissive for SV40. Several continuously growing cell lines have been established from the SV40 infected cultures which express T antigen in 100% of the cells. The results indicate that undifferentiated embryonal carcinoma cells and their differentiated progeny respond quite differently to challenge with these two oncogenic DNA viruses.
    Additional Material: 2 Ill.
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  • 2
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Monolayer cultures of a mouse teratocarcinoma were established in vitro. These cultures contained embryonal carcinoma, the malignant stem cell, and its differentiated progeny: parietal yolk sac, neuroepithelial, and mesenchymal cells. Tissues such as squamous epithelium, cartilage, striated muscle, neuroepithelium, and glands were produced from embryonal carcinoma that was maintained under conditions of long term culture. Frequent subcultivation with pancreatin allowed the establishment of cell lines of embryonal carcinoma which have been maintained for more than 18 months in vitro and continue to produce differentiated cells under specific culture conditions. Chromosomally these lines of embryonal carcinoma have a stem line of 39 chromosomes. Two lines of parietal yolk sac cells have been established which produce basement membrane, are not tumorigenic, and chromosomally are hypotetraploid. This system may yield information concerning neoplastic differentiation and its possible use in therapy for cancer.
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  • 3
    ISSN: 0095-9898
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The transformation process induced by polyoma virus in mass cultures of hamster embryo cells has been analyzed chronologically for several parameters: morphology, karyology, antigenicity and transplantability. Morphological changes, as manifested by the altered growth pattern of the culture, were the first indication of transformation. The expression of morphological transformation differed among colonies from a single culture and among the various cell lines; its pattern could change with prolonged growth of the cultures. Established lines originating from each transformed culture eventually produced tumors in syngeneic and allogeneic animals. Tumorigenicity was low (MTD ± 106) soon after morphological transformation, but increased progressively as the cells were carried in vitro (MTD 〈 103). Polyoma virus disappeared in eight lines, but persisted in one. The non-virus releaser lines were resistant to superinfection with polyoma virus. The polyoma-induced transplantation antigen (PV-ITA) was found in four of six lines; it was not demonstrable in later passages of some lines that were initially positive and was not detected in the virus carrier culture. The polyoma-induced CF antigen (PV-ICFA), however, was present in all the cultures exposed to polyoma virus even at passage levels where the PV-ITA was not demonstrable. Some chromosomal changes in type and in ploidy were present at, or shortly after, the time of morphological transformation. Although very low at first, frequency of chromosome changes increased with time in a random pattern. Three of four lines remained near-diploid, the fourth line became subtetraploid soon after morphological transformation. The incidence of chromosomal damage (chromatid breaks, dicentrics and fragments) was low in all four lines analyzed, even in the virus carrier culture. There was a parallel increase in frequency of abnormal metaphases and of transplantability.It is concluded that after an initial and yet obscure polyoma virus cell interaction, cells evolve toward malignancy in a pattern that does not show specificity for the inducing virus. The viral genome, if present in the transformed cells, does not appear to direct or regulate the evolution of the cells in vitro.
    Additional Material: 9 Ill.
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