Journal article
Inducible mutagenesis in TEPC 2372, a mouse plasmacytoma cell line that harbors the transgenic shuttle vector λLIZ
Mutation research, Vol.473(1), pp.121-136
2001
DOI: 10.1016/S0027-5107(00)00143-3
PMID: 11166031
Abstract
The plasmacytoma cell line, TEPC 2372, was derived from a malignant plasma cell tumor that developed in the peritoneal cavity of a BALB/c mouse that harbored the transgenic shuttle vector for the assessment of mutagenesis in vivo, λLIZ. TEPC 2372 was found to display the typical features of a BALB/c plasmacytoma. It consisted of pleomorphic plasma cells that secreted a monoclonal immunoglobulin (IgG2b/λ), was initially dependent on the presence of IL-6 to grow in cell culture, contained a hyperdiploid chromosome complement with a tendency to undergo tetraploidization, and harbored a constitutively active c-
myc gene by virtue of a T(6;15) chromosomal translocation. TEPC 2372 was further characterized by the ability to respond to in vitro exposure with 4-NQO (4-nitroquinoline-1-oxide), an oxidative model mutagen, with a vigorous dose-dependent increase in mutagenesis that peaked at a 7.85-fold elevation of mutant rates in λLIZ when compared to background mutant rates in untreated controls. Cotreatment with 4-NQO and BSO (buthionine sulfoximine), a glutathione-depleting compound that causes endogenous oxidative stress, resulted in a 9.03-fold increase in the mutant frequency in λLIZ. These results demonstrated that TEPC 2372, the malignant plasma cell counterpart of the λLIZ-based in vivo mutagenesis assay, may be useful as an in vitro reference point for the further elucidation of oxidative mutagenesis in lymphoid tissues.
Details
- Title: Subtitle
- Inducible mutagenesis in TEPC 2372, a mouse plasmacytoma cell line that harbors the transgenic shuttle vector λLIZ
- Creators
- K Felix - Laboratory of Genetics, DBS, NCI, Building 37, Room 2B10, Bethesda, MD 20892-4255, USAA.L Kovalchuk - Laboratory of Genetics, DBS, NCI, Building 37, Room 2B10, Bethesda, MD 20892-4255, USAS.S Park - Laboratory of Genetics, DBS, NCI, Building 37, Room 2B10, Bethesda, MD 20892-4255, USAA.E Coleman - Laboratory of Genetics, DBS, NCI, Building 37, Room 2B10, Bethesda, MD 20892-4255, USAE.S Ramsay - Laboratory of Genetics, DBS, NCI, Building 37, Room 2B10, Bethesda, MD 20892-4255, USAM Qian - Laboratory of Genetics, DBS, NCI, Building 37, Room 2B10, Bethesda, MD 20892-4255, USAK.A Kelliher - Laboratory of Genetics, DBS, NCI, Building 37, Room 2B10, Bethesda, MD 20892-4255, USAG.M Jones - Laboratory of Genetics, DBS, NCI, Building 37, Room 2B10, Bethesda, MD 20892-4255, USAT Ried - Medicine Branch, NCI, NIH, Bethesda, MD, USAG.W Bornkamm - Institute of Molecular Biology and Tumor Genetics, GSF, Munich, GermanyS Janz - Laboratory of Genetics, DBS, NCI, Building 37, Room 2B10, Bethesda, MD 20892-4255, USA
- Resource Type
- Journal article
- Publication Details
- Mutation research, Vol.473(1), pp.121-136
- Publisher
- Elsevier B.V
- DOI
- 10.1016/S0027-5107(00)00143-3
- PMID
- 11166031
- ISSN
- 0027-5107
- eISSN
- 1873-135X
- Language
- English
- Date published
- 2001
- Academic Unit
- Pathology
- Record Identifier
- 9984083831702771
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