J Gen Virol Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Gen Virol 17 (1972), 107-109; DOI 10.1099/0022-1317-17-1-107
© 1972 Society for General Microbiology

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Oie, H. K.
Right arrow Articles by Baron, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Oie, H. K.
Right arrow Articles by Baron, S.
Agricola
Right arrow Articles by Oie, H. K.
Right arrow Articles by Baron, S.

High Interferon Producing Line of Transformed Murine Cells

H. K. Oie, A. F. Gazdar, C. E. Buckler and S. Baron

Laboratory of Viral Diseases National Institute of Allergy and Infectious Diseases and Viral Leukemia and Lymphoma Branch National Cancer Institute National Institutes of Health, Bethesda, Maryland 20014, U.S.A.

During a comparative study of the interferon system in normal and virus-transformed murine cells, a clonal line was observed to produce unusually high yields of interferon. This report describes some variables which influence the interferon yield.

Procedures for the establishment of Moloney sarcoma virus (MSV)-transformed cell clones have been described previously (Bassin, Tuttle & Fischinger, 1970). The twice cloned line C-243-3 was received from Dr. Bassin, National Cancer Institute, Bethesda, Maryland. The line was derived by transforming 3T3FL cells, a subline of the original Swiss 3T3 cell line (Todaro & Green, 1963) under conditions permitting infection by MSV in the absence of associated ‘helper’ leukaemia virus. The cells contain the MSV genome but do not release infectious MSV or leukaemia virus. However, the cells do release small quantities of non-infectious, non-transforming, virus-like particles. Such cells have been termed S + L - cells (Bassin et al. 1970, 1971).

Received 23 May 1972; accepted 4 June 1972.


This article has been cited by other articles:


Home page
J. Cell Sci.Home page
I. Niedick, N. Froese, A. Oumard, P. P. Mueller, M. Nourbakhsh, H. Hauser, and M. Koster
Nucleolar localization and mobility analysis of the NF-{kappa}B repressing factor NRF
J. Cell Sci., July 15, 2004; 117(16): 3447 - 3458.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
A. Oumard, M. Hennecke, H. Hauser, and M. Nourbakhsh
Translation of NRF mRNA Is Mediated by Highly Efficient Internal Ribosome Entry
Mol. Cell. Biol., April 15, 2000; 20(8): 2755 - 2759.
[Abstract] [Full Text]


Home page
ScienceHome page
J De Maeyer-Guignard, A Cachard, and E De Maeyer
Delayed-type hypersensitivity to sheep red blood cells: inhibition of sensitization by interferon
Science, November 7, 1975; 190(4214): 574 - 576.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 1972 by the Society for General Microbiology.