## Abstract Mouse teratocarcinoma cells derived from embryoid bodies of 129SVsl mice were cultured in vitro to permit their differentiation. These cells were then infected with simiam virus 40 (SV40) and 31 cloned cell lines (SVTER) were derived from these cultures. All 31 SVTER cell lines containe
Cell properties after repeated transplantation of spontaneously and of SV40 virus transformed mouse cell lines. I. Growth in culture
β Scribed by V. W. McFarland; P. T. Mora; A. Schultz; S. Pancake
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- English
- Weight
- 769 KB
- Volume
- 85
- Category
- Article
- ISSN
- 0021-9541
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β¦ Synopsis
Abstract
βSpontaneouslyβ or SV40 virus transformed AL/N mouse cell lines were passed repeatedly through syngeneic mice. Cell lines were reβestablished in culture from minced pieces of tumors in the presence of concentrated fetal calf serum or from tumor cells dispersed by trypsin. The aim of this study was to compare the two cell lines in regard to the selection processes which operate during such procedures by characterization of the resulting cell lines. Measurements of growth in tissue culture on substratum showed no significant difference between any of the transformed cell lines. The SV40 transformed cells and its derivative cells had a low anchorage requirement for growth. The greatest anchorage requirement for growth was in the normal untransformed cells and in the derivative cells from the βspontaneouslyβ transformed cells which were established from minced tumors. The spontaneously transformed cells and all derivative cells had high tumorigenicity in vivo (TD~50~ < 10^2^). The SV40 transformed cells had no observable tumorigenicity (TD~50~ > 10^8^), except when injected into irradiated mice (TD~50~ = 10^7^). The derivative cell lines obtained from such a tumor had increased tumorigenicity (TD~50~ = 1β5 Γ 10^5^ in the immunocompetent mice, 5 Γ 10^4^ in the irradiated mice). The SV40 transformed derivative cells maintained their SV40 specific T antigen and their susceptibility to lysis by specific antiserum.
π SIMILAR VOLUMES
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
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