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Homozygous scid/scid;beige/beige mice have low levels of spontaneous or neonatal T cell-induced B cell generation
The autosomal recessive scid mutation results in defective immunoglobulin and T cell receptor gene rearrangement. The scid mutation occurred in the allotype congenic C.B-17 line, and up to 25% of C.B-17 scid mice spontaneously produce both T cells and immunoglobulin, a phenotype known as "leaky...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1993
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190863/ https://www.ncbi.nlm.nih.gov/pubmed/8418200 |
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collection | PubMed |
description | The autosomal recessive scid mutation results in defective immunoglobulin and T cell receptor gene rearrangement. The scid mutation occurred in the allotype congenic C.B-17 line, and up to 25% of C.B-17 scid mice spontaneously produce both T cells and immunoglobulin, a phenotype known as "leaky." Moreover, introduction of neonatal T cells into C.B-17 scid mice leads to immunoglobulin production by 100% of animals. We have produced mice homozygous for both the scid and beige mutations. By contrast with C.B-17 scid mice, BALB/c scid.beige mice have a < 2% incidence of "leakiness." This percentage does not increase with age, and introduction of neonatal T cells fails to rescue immunoglobulin production. This suggests that a gene (or genes) closely linked to the beige locus regulates B and/or T cell development. |
format | Text |
id | pubmed-2190863 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1993 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21908632008-04-16 Homozygous scid/scid;beige/beige mice have low levels of spontaneous or neonatal T cell-induced B cell generation J Exp Med Articles The autosomal recessive scid mutation results in defective immunoglobulin and T cell receptor gene rearrangement. The scid mutation occurred in the allotype congenic C.B-17 line, and up to 25% of C.B-17 scid mice spontaneously produce both T cells and immunoglobulin, a phenotype known as "leaky." Moreover, introduction of neonatal T cells into C.B-17 scid mice leads to immunoglobulin production by 100% of animals. We have produced mice homozygous for both the scid and beige mutations. By contrast with C.B-17 scid mice, BALB/c scid.beige mice have a < 2% incidence of "leakiness." This percentage does not increase with age, and introduction of neonatal T cells fails to rescue immunoglobulin production. This suggests that a gene (or genes) closely linked to the beige locus regulates B and/or T cell development. The Rockefeller University Press 1993-01-01 /pmc/articles/PMC2190863/ /pubmed/8418200 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 Homozygous scid/scid;beige/beige mice have low levels of spontaneous or neonatal T cell-induced B cell generation |
title | Homozygous scid/scid;beige/beige mice have low levels of spontaneous or neonatal T cell-induced B cell generation |
title_full | Homozygous scid/scid;beige/beige mice have low levels of spontaneous or neonatal T cell-induced B cell generation |
title_fullStr | Homozygous scid/scid;beige/beige mice have low levels of spontaneous or neonatal T cell-induced B cell generation |
title_full_unstemmed | Homozygous scid/scid;beige/beige mice have low levels of spontaneous or neonatal T cell-induced B cell generation |
title_short | Homozygous scid/scid;beige/beige mice have low levels of spontaneous or neonatal T cell-induced B cell generation |
title_sort | homozygous scid/scid;beige/beige mice have low levels of spontaneous or neonatal t cell-induced b cell generation |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190863/ https://www.ncbi.nlm.nih.gov/pubmed/8418200 |