## Abstract The host‐virus interactions of Simian virus 40 (SV^40^) 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 derive
Increased susceptibility of murine teratocarcinoma cells to simian virus 40 and polyoma virus following treatment with 5-bromodeoxyuridine
✍ Scribed by Wendell C. Speers; John M. Lehman
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- English
- Weight
- 678 KB
- Volume
- 88
- Category
- Article
- ISSN
- 0021-9541
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✦ Synopsis
Abstract
Cultures of the multipotential stem cell, embryonal carcinoma (EC), of a murine teratocarcinoma were treated with 5‐bromodeoxyuridine (BrdU). Within 2–4 days at concentrations of 1–50 m̈gm/ml of BrdU, there was a marked change in the morphology of cells observed by light and electron microscopy. A comparison of the growth potential showed that for up to four days the BrdU‐treated cultures were similar to untreated cultures. When these BrdU‐treated cells were infected with Simian virus 40 (SV~40~) and polyoma virus (Py), there was an increase in susceptibility of the treated cells. The untreated embryonal carcinoma cells were refractory. These results suggest that BrdU modifies the embryonal carcinoma cells to allow infection with two DNA viruses.
📜 SIMILAR VOLUMES
Multipotential stem cells of a murine teratocarcinoma are resistant to typical infection with either polyoma virus (PV) or Simian virus 40 (SV,o). Differentiated progeny of the stem cells are susceptible to infection in a manner identical to other mouse somatic cells, i.e., they are permissive for P