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Ontogeny of Ia and IgD on IgM-bearing B lymphocytes in mice
We used immunofluorescence to examine the developmental relationship of Ia and IgD on B cells. Pre-B cells in fetal liver did not express Ia. Only very few surface IgM-positive (sIgM+) B cells in fetal spleen were found to be Ia+ and were weakly stained for Ia. After birth there was a linear increas...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1977
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2180751/ https://www.ncbi.nlm.nih.gov/pubmed/301548 |
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collection | PubMed |
description | We used immunofluorescence to examine the developmental relationship of Ia and IgD on B cells. Pre-B cells in fetal liver did not express Ia. Only very few surface IgM-positive (sIgM+) B cells in fetal spleen were found to be Ia+ and were weakly stained for Ia. After birth there was a linear increase in the proportion of sIgM+ spleen cells which expressed Ia, reaching 95% by 9 days. Adult bone marrow also contains a sizeable proportion of sIgM+ Ia- cells. Unstimulated cells from fetal or newborn liver and spleen expressed Ia at the same rate in culture. Anti-Ia antisera suppressed the LPS-induced differentiation of IgM and IgG plasma cells in cultures of neonatal lymphocytes. Ia was also detected on IgM and IgG plasma cells in vitro suggesting that lipopolysaccharide (LPS)-stimulated B cells by may express Ia antigens, induced by LPS, or appearing as part of normal differentiation. IgD did not appear on sIgM+ cells until 3 days of age and then rose slowly to reach adult levels later than Ia antigens. |
format | Text |
id | pubmed-2180751 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1977 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21807512008-04-17 Ontogeny of Ia and IgD on IgM-bearing B lymphocytes in mice J Exp Med Articles We used immunofluorescence to examine the developmental relationship of Ia and IgD on B cells. Pre-B cells in fetal liver did not express Ia. Only very few surface IgM-positive (sIgM+) B cells in fetal spleen were found to be Ia+ and were weakly stained for Ia. After birth there was a linear increase in the proportion of sIgM+ spleen cells which expressed Ia, reaching 95% by 9 days. Adult bone marrow also contains a sizeable proportion of sIgM+ Ia- cells. Unstimulated cells from fetal or newborn liver and spleen expressed Ia at the same rate in culture. Anti-Ia antisera suppressed the LPS-induced differentiation of IgM and IgG plasma cells in cultures of neonatal lymphocytes. Ia was also detected on IgM and IgG plasma cells in vitro suggesting that lipopolysaccharide (LPS)-stimulated B cells by may express Ia antigens, induced by LPS, or appearing as part of normal differentiation. IgD did not appear on sIgM+ cells until 3 days of age and then rose slowly to reach adult levels later than Ia antigens. The Rockefeller University Press 1977-07-01 /pmc/articles/PMC2180751/ /pubmed/301548 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 Ontogeny of Ia and IgD on IgM-bearing B lymphocytes in mice |
title | Ontogeny of Ia and IgD on IgM-bearing B lymphocytes in mice |
title_full | Ontogeny of Ia and IgD on IgM-bearing B lymphocytes in mice |
title_fullStr | Ontogeny of Ia and IgD on IgM-bearing B lymphocytes in mice |
title_full_unstemmed | Ontogeny of Ia and IgD on IgM-bearing B lymphocytes in mice |
title_short | Ontogeny of Ia and IgD on IgM-bearing B lymphocytes in mice |
title_sort | ontogeny of ia and igd on igm-bearing b lymphocytes in mice |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2180751/ https://www.ncbi.nlm.nih.gov/pubmed/301548 |