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Susceptibility to in vitro tolerance induction of adult B cells from mice with an X-linked B-cell defect
Previous studies from this laboratory have indicated that the susceptibility to in vitro tolerance induction is restricted to B cells early in their development (12,14). In this study, a modification of the in vitro splenic focus technique was used to determine whether 2,4- dinitrophenyl (DNP)-speci...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1980
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2185773/ https://www.ncbi.nlm.nih.gov/pubmed/6965400 |
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collection | PubMed |
description | Previous studies from this laboratory have indicated that the susceptibility to in vitro tolerance induction is restricted to B cells early in their development (12,14). In this study, a modification of the in vitro splenic focus technique was used to determine whether 2,4- dinitrophenyl (DNP)-specific splenic B cells from adult (CBA/N X DBA/2)F1 males are susceptible to in vitro tolerance induction. The results demonstrate that greater than 50% of the DNP-specific B cells in the adult F1 male are tolerizable and therefore immature by this criterion. Moreover, the findings define at least two subpopulation in adult CBA/N mice, one of which is tolerizable. These findings are consistent with the hypothesis that the lymphoid population in the adult CBA/N mouse is characteristic of a neonatal B-cell population. |
format | Text |
id | pubmed-2185773 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1980 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21857732008-04-17 Susceptibility to in vitro tolerance induction of adult B cells from mice with an X-linked B-cell defect J Exp Med Articles Previous studies from this laboratory have indicated that the susceptibility to in vitro tolerance induction is restricted to B cells early in their development (12,14). In this study, a modification of the in vitro splenic focus technique was used to determine whether 2,4- dinitrophenyl (DNP)-specific splenic B cells from adult (CBA/N X DBA/2)F1 males are susceptible to in vitro tolerance induction. The results demonstrate that greater than 50% of the DNP-specific B cells in the adult F1 male are tolerizable and therefore immature by this criterion. Moreover, the findings define at least two subpopulation in adult CBA/N mice, one of which is tolerizable. These findings are consistent with the hypothesis that the lymphoid population in the adult CBA/N mouse is characteristic of a neonatal B-cell population. The Rockefeller University Press 1980-02-01 /pmc/articles/PMC2185773/ /pubmed/6965400 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 Susceptibility to in vitro tolerance induction of adult B cells from mice with an X-linked B-cell defect |
title | Susceptibility to in vitro tolerance induction of adult B cells from mice with an X-linked B-cell defect |
title_full | Susceptibility to in vitro tolerance induction of adult B cells from mice with an X-linked B-cell defect |
title_fullStr | Susceptibility to in vitro tolerance induction of adult B cells from mice with an X-linked B-cell defect |
title_full_unstemmed | Susceptibility to in vitro tolerance induction of adult B cells from mice with an X-linked B-cell defect |
title_short | Susceptibility to in vitro tolerance induction of adult B cells from mice with an X-linked B-cell defect |
title_sort | susceptibility to in vitro tolerance induction of adult b cells from mice with an x-linked b-cell defect |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2185773/ https://www.ncbi.nlm.nih.gov/pubmed/6965400 |