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Elevated myc expression and c-myc amplification in spontaneously occurring B lymphoid cell lines

Recently, a minor subpopulation of murine B lymphocytes, Ly-1+ B cells, has been distinguished by its unique ontogeny, tissue distribution, and prominence in certain autoimmune and neoplastic B cell diseases. We have previously described a simple murine spleen culture system that results in the spon...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1987
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188571/
https://www.ncbi.nlm.nih.gov/pubmed/3549960
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description Recently, a minor subpopulation of murine B lymphocytes, Ly-1+ B cells, has been distinguished by its unique ontogeny, tissue distribution, and prominence in certain autoimmune and neoplastic B cell diseases. We have previously described a simple murine spleen culture system that results in the spontaneous and exclusive outgrowth of long-term Ly-1+ B cell lines (B Ly-1 cells). Here, we report that the immortal growth property of B Ly-1 cells correlates with a 10-45-fold elevation of steady-state myc RNA and 2-10-fold amplification of the c-myc locus. While c-myc amplification has been observed in malignant cell lines derived from several tissues of origin, its occurrence in lymphoid cells has not been previously reported. The consistent c-myc amplification in B Ly-1 cells may reflect a unique state of this locus in the Ly-1+ B lymphocyte lineage, and contribute to the spontaneous immortalization of this B cell population in vitro, and its apparent predilection for malignant transformation in vivo.
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spelling pubmed-21885712008-04-17 Elevated myc expression and c-myc amplification in spontaneously occurring B lymphoid cell lines J Exp Med Articles Recently, a minor subpopulation of murine B lymphocytes, Ly-1+ B cells, has been distinguished by its unique ontogeny, tissue distribution, and prominence in certain autoimmune and neoplastic B cell diseases. We have previously described a simple murine spleen culture system that results in the spontaneous and exclusive outgrowth of long-term Ly-1+ B cell lines (B Ly-1 cells). Here, we report that the immortal growth property of B Ly-1 cells correlates with a 10-45-fold elevation of steady-state myc RNA and 2-10-fold amplification of the c-myc locus. While c-myc amplification has been observed in malignant cell lines derived from several tissues of origin, its occurrence in lymphoid cells has not been previously reported. The consistent c-myc amplification in B Ly-1 cells may reflect a unique state of this locus in the Ly-1+ B lymphocyte lineage, and contribute to the spontaneous immortalization of this B cell population in vitro, and its apparent predilection for malignant transformation in vivo. The Rockefeller University Press 1987-04-01 /pmc/articles/PMC2188571/ /pubmed/3549960 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
Elevated myc expression and c-myc amplification in spontaneously occurring B lymphoid cell lines
title Elevated myc expression and c-myc amplification in spontaneously occurring B lymphoid cell lines
title_full Elevated myc expression and c-myc amplification in spontaneously occurring B lymphoid cell lines
title_fullStr Elevated myc expression and c-myc amplification in spontaneously occurring B lymphoid cell lines
title_full_unstemmed Elevated myc expression and c-myc amplification in spontaneously occurring B lymphoid cell lines
title_short Elevated myc expression and c-myc amplification in spontaneously occurring B lymphoid cell lines
title_sort elevated myc expression and c-myc amplification in spontaneously occurring b lymphoid cell lines
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188571/
https://www.ncbi.nlm.nih.gov/pubmed/3549960