A Mus dunni cell line that lacks sequences closely related to endogenous murine leukemia viruses and can be infected by ectropic, amphotropic, xenotropic, and mink cell focus-forming viruses
- 1 November 1984
- journal article
- research article
- Published by American Society for Microbiology in Journal of Virology
- Vol. 52 (2) , 695-8
- https://doi.org/10.1128/jvi.52.2.695-698.1984
Abstract
A Mus dunni cell line has been developed that is permissive for all four classes of murine leukemia viruses (MuLV): ecotropic, amphotropic, xenotropic, and mink cell focus-forming viruses. The M. dunni cells contain fewer MuLV-related sequences than do feral or domestic mouse, rat, or mink cells. Infection of the line by ecotropic MuLV induces a distinct cytopathic effect, and the cells can be readily transfected by MuLV DNA. The M. dunni line has been used to isolate an endogenous MuLV from the SC-1 feral mouse cell line.Keywords
This publication has 12 references indexed in Scilit:
- Interference grouping of murine leukemia viruses: A distinct receptor for the MCF-Recombinant viruses in mouse cellsVirology, 1982
- Cellular origin and role of mink cell focus-forming viruses in murine thymic lymphomasNature, 1982
- Origin of mink cytopathic focus-forming (MCF) viruses:Comparison with ecotropic and xenotropic murine leukemia virus genomesVirology, 1981
- A new class of murine leukemia virus associated with development of spontaneous lymphomas.Proceedings of the National Academy of Sciences, 1977
- Clonal cell lines from a feral mouse embryo which lack host-range restrictions for murine leukemia virusesVirology, 1975
- Mink cell line MvlLu (CCL 64)Virology, 1974
- Xenotropic Viruses: Murine Leukemia Viruses Associated with NIH Swiss, NZB, and Other Mouse StrainsScience, 1973
- Plaque assay techniques for murine leukemia virusesVirology, 1970
- Host-Range Restrictions of Murine Leukemia Viruses in Mouse Embryo Cell CulturesJournal of Virology, 1970
- Development of 3T3‐like lines from Balb/c mouse embryo cultures: Transformation susceptibility to SV40Journal of Cellular Physiology, 1968