## Abstract A horse skin cell line (E. Derm, NBL‐6, CCL‐57) was susceptible to focus formation by the Kirsten mouse sarcoma virus, feline sarcoma virus (ST strain) and the MSV pseudotypes with woolly monkey, gibbon monkey, RD‐114, AT‐124, baboon placenta and murine xenotropic (BALB/c 3T3 and C57L/J
Neoplastic transformation of rabbit cells by murine sarcoma viruses
✍ Scribed by J. S. Rhim; H. G. Bedigian; R. R. Fox
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- French
- Weight
- 703 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Neoplastic transformation of rabbit cells by Kirsten murine sarcoma virus (Ki‐MSV), the Ki‐MSV pseudotype of baboon endogenous virus (Ki‐MSV[BaEV]) and the Moloney‐MSV pseudotype of feline leukemia virus (M‐MSV[FeLV]) is reported. Rabbit cells can be readily transformed by Ki‐MSV, Ki‐MSV(BaEV) and M‐MSV(FeLV). Rabbit cells transformed by Ki‐MSV and M‐MSV(FeLV) were found to be virus producers, whereas those transformed by Ki‐MSV(BaEV) were nonproducers (NP). The NP cells were obtained by simply infection rabbit cells with Ki‐MSV(BaEV) and subculturing the infected cells. Although the morphologically altered NP cells did not produce infectious virus or murine leukemia virus antigen, they did contain a rescuable MSV genome. All of the transformed cells formed colonies in soft agar, grew to high saturation densities and produced tumors when transplanted into nude mice. The Ki‐MSV and M‐MSV(FeLV)‐transformed cells produced tumors in newborn WH/J rabbits, thus providing an important tool for studying tumor immunity in the rabbit.
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