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A Transgenic Marker for Mouse B Lymphoid Precursors

Three lines of transgenic mice have been generated which express human CD25 under the control of the 722-base pair region located immediately 5′ of the precursor (pre)–B cell–specific λ5 gene. All three strains express human CD25 in parallel to endogenous λ5 on pre–B cells, but not on mature B lymph...

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Detalles Bibliográficos
Autores principales: Mårtensson, Inga-Lill, Melchers, Fritz, Winkler, Thomas H.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2196144/
https://www.ncbi.nlm.nih.gov/pubmed/9034144
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author Mårtensson, Inga-Lill
Melchers, Fritz
Winkler, Thomas H.
author_facet Mårtensson, Inga-Lill
Melchers, Fritz
Winkler, Thomas H.
author_sort Mårtensson, Inga-Lill
collection PubMed
description Three lines of transgenic mice have been generated which express human CD25 under the control of the 722-base pair region located immediately 5′ of the precursor (pre)–B cell–specific λ5 gene. All three strains express human CD25 in parallel to endogenous λ5 on pre–B cells, but not on mature B lymphocytes or other blood cell lineages. High expression of human CD25 on B lineage cells of transgenic mice has allowed the identification of a new B220(+)CD19(−)λ5(+) precursor of the B220(+)CD19(+)λ5(+) c-kit(+) pre-BI cells. Both types of precursors are clonable on stromal cells in the presence of interleukin-7. The CD19(−) precursors have a sizeable part of their immunoglobulin heavy chain gene loci in germline configuration, while the CD19(+) pre–BI cells are predominantly DJ(H) rearranged. The results indicate that random integration of the 722-bp 5′ region of the λ5 gene into the mouse genome confers tissue and differentiation stage–specific expression of a transgene.
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spelling pubmed-21961442008-04-16 A Transgenic Marker for Mouse B Lymphoid Precursors Mårtensson, Inga-Lill Melchers, Fritz Winkler, Thomas H. J Exp Med Article Three lines of transgenic mice have been generated which express human CD25 under the control of the 722-base pair region located immediately 5′ of the precursor (pre)–B cell–specific λ5 gene. All three strains express human CD25 in parallel to endogenous λ5 on pre–B cells, but not on mature B lymphocytes or other blood cell lineages. High expression of human CD25 on B lineage cells of transgenic mice has allowed the identification of a new B220(+)CD19(−)λ5(+) precursor of the B220(+)CD19(+)λ5(+) c-kit(+) pre-BI cells. Both types of precursors are clonable on stromal cells in the presence of interleukin-7. The CD19(−) precursors have a sizeable part of their immunoglobulin heavy chain gene loci in germline configuration, while the CD19(+) pre–BI cells are predominantly DJ(H) rearranged. The results indicate that random integration of the 722-bp 5′ region of the λ5 gene into the mouse genome confers tissue and differentiation stage–specific expression of a transgene. The Rockefeller University Press 1997-02-17 /pmc/articles/PMC2196144/ /pubmed/9034144 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 Article
Mårtensson, Inga-Lill
Melchers, Fritz
Winkler, Thomas H.
A Transgenic Marker for Mouse B Lymphoid Precursors
title A Transgenic Marker for Mouse B Lymphoid Precursors
title_full A Transgenic Marker for Mouse B Lymphoid Precursors
title_fullStr A Transgenic Marker for Mouse B Lymphoid Precursors
title_full_unstemmed A Transgenic Marker for Mouse B Lymphoid Precursors
title_short A Transgenic Marker for Mouse B Lymphoid Precursors
title_sort transgenic marker for mouse b lymphoid precursors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2196144/
https://www.ncbi.nlm.nih.gov/pubmed/9034144
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