Rapid cytopathic changes and transformation in human foreskin cell cultures infected with simian virus 40 |
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Authors: | G Petursson J Fogh E De Harven D Armstrong |
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Affiliation: | 1. Sloan-Kettering Institute for Cancer Research, New York, New York, USA;2. Sloan-Kettering Division, Cornell University Medical College, New York, New York, USA;3. Children''s Hospital of Philadelphia, Philadelphia, Pennsylvania, USA;1. Blood Center of Ribeirão Preto, Faculty of Medicine of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil;2. Laboratório de Flavivírus, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Rio de Janeiro, Rio de Janeiro, Brazil;3. Department of Science and Technology for Humans and the Environment, University of Campus Bio-Medico di Roma, Rome, Italy;4. Department of Morphology, Faculty of Medicine of the Federal University of Santa Maria, Santa Maria, Rio Grande do Sul, Brazil;5. Euro-American University Center, UNIEURO, Brasília, Federal District, Brazil;6. Blood Center of Brasília, Brasília, Federal District, Brazil;7. Faculty of Ceilandia, University of Brasília, Brasília, Federal District, Brazil;8. Institute of Hematology and Hemotherapy of Amapa, Macapa, Amapa, Brazil;9. Epidemiology and Statistic Unit, University of Campus Bio-Medico di Roma, Rome, Italy;10. Butantan Institute, São Paulo, São Paulo, Brazil;1. Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR, USA;2. Department of Pathology, New York University School of Medicine, New York, NY, USA;3. Molsoft, La Jolla, CA, USA;4. Icahn School of Medicine at Mount Sinai, New York, NY, USA;1. Okazaki Institute for Integrative Bioscience, National Institute for Basic Biology, and National Institutes of Natural Sciences, 5-1 Higashiyama, Myodaiji, Okazaki, Aichi 444-8787, Japan;2. Shimane Agricultural Experiment Station, Izumo, Shimane 693-0035, Japan;3. Department of Science of Technology Innovation, Nagaoka University of Technology, Nagaoka, Niigata 940-2188, Japan |
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Abstract: | Human foreskin cells exposed to SV40 exhibited characteristic cytopathic changes as early as 2 days after infection. The changes, occurring much sooner than in other reported human cells, included enlargement of nuclei and nucleoli, formation of multiple eosinophilic nuclear inclusions, and basophilic RNA-containing bodies in the cytoplasm. The nuclei showed bright fluorescence of various patterns with the indirect Coons' method. During the following days cell destruction occurred simultaneously with increased cell proliferation. Foci of rapidly dividing transformed cells appeared 3–4 weeks after infection. The transformed cells also differed from untransformed cells in morphology and growth pattern, showing many abnormal mitoses, and were more easily suspended by trypsinization. Virus was released, but in decreasing amounts, with serial passage of the transformed cell cultures. Occasional cells with typical cytopathic nuclear changes and specific nuclear immunofluorescence were present in the seventh passage after transformation. The demonstration of the SV40 complement-fixing tumor antigen in the transformed cells confirmed the specificity of the transformation. Electron microscope evidence for the early intranuclear multiplication of the virus and preliminary observations of the ultrastructure of the transformed cells are presented. |
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