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Restricted expression of ecotropic virus by thymocytes of leukemia- resistant (AKR X NZB)F1 mice

AKR mice, which produce high titers of ecotropic virus, were crossed with NZB mice, which produce titers of xenotropic virus. Spleen, marrow, and lymph node cells of the F1 hybrid produced high titers of ecotropic and xenotropic viruses. However, expression of ecotropic virus by both thymus cells an...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1978
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2184930/
https://www.ncbi.nlm.nih.gov/pubmed/209123
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description AKR mice, which produce high titers of ecotropic virus, were crossed with NZB mice, which produce titers of xenotropic virus. Spleen, marrow, and lymph node cells of the F1 hybrid produced high titers of ecotropic and xenotropic viruses. However, expression of ecotropic virus by both thymus cells and peripheral T cells of the F1 was severely restricted. Despite simultaneous expression of ecotorpic and xenotropic viruses in F1 spleens, lymph nodes, and marrows evidence for recombinant viruses was not found. Such viruses were also undetectable in the F1 thymuses. The results indicate that a cellular mechanism, present in AKR thymus but lacking in the F1 influences virus expression and the formation of recombinant viruses. This may account for the low incidence of leukemia in the F1 hybrid.
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spelling pubmed-21849302008-04-17 Restricted expression of ecotropic virus by thymocytes of leukemia- resistant (AKR X NZB)F1 mice J Exp Med Articles AKR mice, which produce high titers of ecotropic virus, were crossed with NZB mice, which produce titers of xenotropic virus. Spleen, marrow, and lymph node cells of the F1 hybrid produced high titers of ecotropic and xenotropic viruses. However, expression of ecotropic virus by both thymus cells and peripheral T cells of the F1 was severely restricted. Despite simultaneous expression of ecotorpic and xenotropic viruses in F1 spleens, lymph nodes, and marrows evidence for recombinant viruses was not found. Such viruses were also undetectable in the F1 thymuses. The results indicate that a cellular mechanism, present in AKR thymus but lacking in the F1 influences virus expression and the formation of recombinant viruses. This may account for the low incidence of leukemia in the F1 hybrid. The Rockefeller University Press 1978-07-01 /pmc/articles/PMC2184930/ /pubmed/209123 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Restricted expression of ecotropic virus by thymocytes of leukemia- resistant (AKR X NZB)F1 mice
title Restricted expression of ecotropic virus by thymocytes of leukemia- resistant (AKR X NZB)F1 mice
title_full Restricted expression of ecotropic virus by thymocytes of leukemia- resistant (AKR X NZB)F1 mice
title_fullStr Restricted expression of ecotropic virus by thymocytes of leukemia- resistant (AKR X NZB)F1 mice
title_full_unstemmed Restricted expression of ecotropic virus by thymocytes of leukemia- resistant (AKR X NZB)F1 mice
title_short Restricted expression of ecotropic virus by thymocytes of leukemia- resistant (AKR X NZB)F1 mice
title_sort restricted expression of ecotropic virus by thymocytes of leukemia- resistant (akr x nzb)f1 mice
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2184930/
https://www.ncbi.nlm.nih.gov/pubmed/209123