## Abstract A pseudodiploid clone of Chinese hamster cells transformed in vitro with Simian virus 40 (SV~40~) was isolated from soft agar and injected into nude mice through three successive passages with a short in vitro cultivation between each animal inoculation. The original clone and the three
Simian virus 40 a gene function: Further characterization and growth of tsA transformed Chinese hamster cells
β Scribed by Christine C. Robinson; John M. Lehman
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 929 KB
- Volume
- 111
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Chinese hamster embryo cells transformed with the tsA 58 mutant of Simian virus 40 express the transformed phenotype at the permissive temperature (33Β°C or 37Β°C) and a βnormalβ phenotype at the nonpermissive temperature (40.5Β°C). Immunofluorescence and immunoprecipitation of T antigens demonstrated that the βTβ antigen (100 K) has an increase rate of synthesis and degradation at 40.5Β°C. However, the cells continue to replicate at the nonpermissive temperature when assayed by flow cytometry and autoradiography. This DNA synthesis was cellular, not viral, and not owing to an increase in DNA repair. When the cell cycle distributions of G~1~, S, and G~2~ + M were assayed by the fraction labeled mitoses method, no differences were evident at the permissive and nonpermissive temperature; however, the doubling time was lengthened at 40.5Β°C, the tsA transformed cells are cycling and dying. However, if the transformed cells are seeded onto monolayers of normal Chinese hamster cells at 40.5Β°C, the cells are growth arrested when measured by growth assays, flow cytometry, autoradiography, and immunofluorescence for T antigen. Therefore, growth arrest can be obtained in tsA 58 transformed Chinese hamster cells when cocultured with normal Chinese hamster cells.
π SIMILAR VOLUMES
## Abstract Infection of secondary Chinese hamster cells with SV40 virus induces a population of cells into consecutive S periods. These changes in DNA content were examined at various times post infection by means of flow microfluorometry (FMF) which enabled a kinetic analysis to be made. At 12 h
The levels of simian virus 40 (SV40) large T antigen in a tsA-transformed mouse macrophage line at the permissive (33 degrees C) and the nonpermissive (39 degrees C) temperature were examined by immunofluorescence, sodium dodecylsulfate-polyacrylamide gel electrophoresis, complement fixation, and en
It was shown previously that mouse bone marrow cells transformed by simian virus 40 (SV40) show a reversible cell density-dependent phenotypic transition between the nonmacrophage (rapidly growing) and the macrophage (stationary) states; cells in low-density cultures are in the growing phase, expres
Abbreviations: ECM, extracellular matrix; SV40, simian virus 40; a-SMA, a-smooth cells were isolated from a single animal to develop homogeneous muscle actin; TGF-b1, transforming growth factor b1; PCR, polymerase chain reaction.
Cultures of mouse macrophage cell lines transformed by wild-type or the tsA640 mutant of simian virus 40 (SV40) show a reversible phenotypic transition between the nonmacrophage (proliferating phase) and the macrophage (stationary phase) states (Takayama, 1980; Tanigawa et al., 1983). Distribution o