Cargando…
Abnormal ratio of membrane immunoglobulin classes in mice with an X- linked B-lymphocyte defect
CBA/N mice have an X-linked genetic defect in B-lymphocyte function manifested by inability to make antibody responses to T-independent antigens. Plasma membrane immunoglobulin (Ig) on spleen, lymph node, and Peyer's patch cells was analyzed by lactoperoxidase-catalyzed iodination, NP-40 extrac...
Formato: | Texto |
---|---|
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
1975
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189974/ https://www.ncbi.nlm.nih.gov/pubmed/1081577 |
_version_ | 1782146740435025920 |
---|---|
collection | PubMed |
description | CBA/N mice have an X-linked genetic defect in B-lymphocyte function manifested by inability to make antibody responses to T-independent antigens. Plasma membrane immunoglobulin (Ig) on spleen, lymph node, and Peyer's patch cells was analyzed by lactoperoxidase-catalyzed iodination, NP-40 extraction, specific immunoprecipitation, and sodium dodecyl sulfate-polyacrylamide gel electrophoresis. These studies indicated that the X-linked immune defect was associated, in all three cell types, with a decrease in the ratio of cell membrane IgD analog to cell membrane IgM. This suggests either that IgD analog may be important in initiation of T-independent antibody responses or that CBA/N mice lack a subpopulation of B cells specialized to respond to T- independent antigens, and that these cells are relatively rich in plasma membrane IgD analog. |
format | Text |
id | pubmed-2189974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1975 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21899742008-04-17 Abnormal ratio of membrane immunoglobulin classes in mice with an X- linked B-lymphocyte defect J Exp Med Articles CBA/N mice have an X-linked genetic defect in B-lymphocyte function manifested by inability to make antibody responses to T-independent antigens. Plasma membrane immunoglobulin (Ig) on spleen, lymph node, and Peyer's patch cells was analyzed by lactoperoxidase-catalyzed iodination, NP-40 extraction, specific immunoprecipitation, and sodium dodecyl sulfate-polyacrylamide gel electrophoresis. These studies indicated that the X-linked immune defect was associated, in all three cell types, with a decrease in the ratio of cell membrane IgD analog to cell membrane IgM. This suggests either that IgD analog may be important in initiation of T-independent antibody responses or that CBA/N mice lack a subpopulation of B cells specialized to respond to T- independent antigens, and that these cells are relatively rich in plasma membrane IgD analog. The Rockefeller University Press 1975-11-01 /pmc/articles/PMC2189974/ /pubmed/1081577 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 Abnormal ratio of membrane immunoglobulin classes in mice with an X- linked B-lymphocyte defect |
title | Abnormal ratio of membrane immunoglobulin classes in mice with an X- linked B-lymphocyte defect |
title_full | Abnormal ratio of membrane immunoglobulin classes in mice with an X- linked B-lymphocyte defect |
title_fullStr | Abnormal ratio of membrane immunoglobulin classes in mice with an X- linked B-lymphocyte defect |
title_full_unstemmed | Abnormal ratio of membrane immunoglobulin classes in mice with an X- linked B-lymphocyte defect |
title_short | Abnormal ratio of membrane immunoglobulin classes in mice with an X- linked B-lymphocyte defect |
title_sort | abnormal ratio of membrane immunoglobulin classes in mice with an x- linked b-lymphocyte defect |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189974/ https://www.ncbi.nlm.nih.gov/pubmed/1081577 |