Distinct helper virus requirements for Abelson murine leukemia virus-induced pre-B- and T-cell lymphomas.

Détails

ID Serval
serval:BIB_74ECCA157950
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Distinct helper virus requirements for Abelson murine leukemia virus-induced pre-B- and T-cell lymphomas.
Périodique
Journal of Virology
Auteur(s)
Poirier Y., Jolicoeur P.
ISSN
0022-538X (Print)
ISSN-L
0022-538X
Statut éditorial
Publié
Date de publication
1989
Volume
63
Numéro
5
Pages
2088-2098
Langue
anglais
Résumé
Abelson murine leukemia virus (A-MuLV) can induce pre-B- or T-cell lymphomas (thymomas) in mice depending on the route and time of injection. Previous studies have shown that the choice of the helper virus used to rescue A-MuLV greatly influences its ability to induce pre-B-cell lymphomas. In this study, we investigated the role of the helper virus in A-MuLV-induced thymomas. A-MuLV rescued with the helper Moloney MuLV, BALB/c endogenous N-tropic MuLV, and two chimeric MuLVs derived from these two parents were injected intrathymically in young adult NIH Swiss mice. All four A-MuLV pseudotypes were found to be equally efficient in the induction of thymomas, whereas drastic differences were observed in their pre-B-cell lymphomagenic potential. Thymoma induction by A-MuLV was independent of the replication potential of the helper virus in the thymus, and no helper proviral sequences could be detected in the majority of thymomas induced by A-MuLV rescued with parental BALB/c endogenous or chimeric MuLVs. In the thymomas in which helper proviruses were present, none of them were found integrated in the Ahi-1 region, a common proviral integration site found in A-MuLV-induced pre-B-cell lymphomas (Y. Poirer, C. Kozak, and P. Jolicoeur, J. Virol. 62:3985-3992, 1988). In addition, helper-free stocks of A-MuLV were found to be as lymphomagneic as other pseudotypes in inducing thymomas after intrathymic inoculation, in contrast to their inability to induce pre-B-cell lymphomas when injected intraperitoneally in newborn mice. Restriction enzyme analysis revealed one to three A-MuLV proviruses in each thymoma, indicating the oligoclonality of these tumors. Analysis of the immunoglobulin and T-cell receptor loci confirmed that the major population of cells of these primary thymomas belongs to the T-cell lineage. Together, these results indicate that the helper virus has no effect in the induction of A-MuLV-induced T-cell lymphomas, in contrast to its important role in the induction of A-MuLV-induced pre-B-cell lymphomas. Our data also revealed distinct biological requirements for transformation of these two target cells by v-abl.
Mots-clé
Abelson murine leukemia virus/genetics, Abelson murine leukemia virus/pathogenicity, Animals, B-Lymphocytes, Blotting, Southern, Cell Transformation, Viral, DNA, Neoplasm/genetics, Gene Rearrangement, B-Lymphocyte, Gene Rearrangement, T-Lymphocyte, Helper Viruses/genetics, Helper Viruses/pathogenicity, Leukemia Virus, Murine/pathogenicity, Leukemia, Lymphocytic, Chronic, B-Cell/microbiology, Mice, Oncogenes, T-Lymphocytes, Thymoma/microbiology, Virus Replication
Pubmed
Web of science
Création de la notice
26/02/2008 13:01
Dernière modification de la notice
03/03/2018 18:22
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