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REGULATION OF CELLULAR ANTIBODY SYNTHESIS : CELLULAR 7S PRODUCTION AND LONGEVITY OF 7S ANTIGEN-SENSITIVE CELLS IN THE ABSENCE OF ANTIBODY FEEDBACK
Transfer of spleen cells from mice immunized against sheep red blood cells (SRBC) into irradiated (600 R) nonimmune, syngeneic mice in the presence of antigen resulted in excessive cellular 7S production 7 days later. The number of 7S plaque-forming cells usually exceeded 10(6) per spleen and the me...
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
1968
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2138442/ https://www.ncbi.nlm.nih.gov/pubmed/5635380 |
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author | Möller, Göran |
author_facet | Möller, Göran |
author_sort | Möller, Göran |
collection | PubMed |
description | Transfer of spleen cells from mice immunized against sheep red blood cells (SRBC) into irradiated (600 R) nonimmune, syngeneic mice in the presence of antigen resulted in excessive cellular 7S production 7 days later. The number of 7S plaque-forming cells usually exceeded 10(6) per spleen and the mean proportion varied between 1 and 70%. In occasional animals all spleen cells were producing antibodies to SRBC. Serum antibody synthesis was also excessively increased, the titers in agglutination after 2-ME treatment and in hemolysis varying between 2(15) and 2(25). The generation time of the 7S PFC was found to be 9.6 hr in the secondary hosts. It seemed possible that the excessive production of 7S PFC and antibodies in the irradiated nonimmune recipients was caused by the absence of feedback inhibition of the immune response by antibody, a mechanism which would normally function to restrict antibody synthesis. This conclusion was strengthened by the demonstration that transfer of antigen-stimulated immune cells into actively or passively immunized irradiated recipients resulted in a marked suppression of cellular 7S synthesis. Serial transfers of antigen-stimulated immune cell populations in irradiated hosts resulted in an equally high number of 7S PFC during the first four transfer generations. However, after the fifth to seventh transfer generation the number of 7S PFC rapidly declined and disappeared within one to three passages. Serum antibodies and 7S PFC declined in parallel during the last transfer generations. Further passages of antigen-stimulated spleen cells lacking 7S PFC did not lead to reappearance of PFC. Thus, antigen-sensitive cells have a limited lifespan and/or multiplication capacity. From the hypothesis that the 7S PFC developed by division from antigen-sensitive precursors it was calculated that 38–40 divisions occurred, Thus, one antigen-sensitive precursor has the potential to give rise to 10(12) 7S PFC. |
format | Text |
id | pubmed-2138442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1968 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21384422008-04-17 REGULATION OF CELLULAR ANTIBODY SYNTHESIS : CELLULAR 7S PRODUCTION AND LONGEVITY OF 7S ANTIGEN-SENSITIVE CELLS IN THE ABSENCE OF ANTIBODY FEEDBACK Möller, Göran J Exp Med Article Transfer of spleen cells from mice immunized against sheep red blood cells (SRBC) into irradiated (600 R) nonimmune, syngeneic mice in the presence of antigen resulted in excessive cellular 7S production 7 days later. The number of 7S plaque-forming cells usually exceeded 10(6) per spleen and the mean proportion varied between 1 and 70%. In occasional animals all spleen cells were producing antibodies to SRBC. Serum antibody synthesis was also excessively increased, the titers in agglutination after 2-ME treatment and in hemolysis varying between 2(15) and 2(25). The generation time of the 7S PFC was found to be 9.6 hr in the secondary hosts. It seemed possible that the excessive production of 7S PFC and antibodies in the irradiated nonimmune recipients was caused by the absence of feedback inhibition of the immune response by antibody, a mechanism which would normally function to restrict antibody synthesis. This conclusion was strengthened by the demonstration that transfer of antigen-stimulated immune cells into actively or passively immunized irradiated recipients resulted in a marked suppression of cellular 7S synthesis. Serial transfers of antigen-stimulated immune cell populations in irradiated hosts resulted in an equally high number of 7S PFC during the first four transfer generations. However, after the fifth to seventh transfer generation the number of 7S PFC rapidly declined and disappeared within one to three passages. Serum antibodies and 7S PFC declined in parallel during the last transfer generations. Further passages of antigen-stimulated spleen cells lacking 7S PFC did not lead to reappearance of PFC. Thus, antigen-sensitive cells have a limited lifespan and/or multiplication capacity. From the hypothesis that the 7S PFC developed by division from antigen-sensitive precursors it was calculated that 38–40 divisions occurred, Thus, one antigen-sensitive precursor has the potential to give rise to 10(12) 7S PFC. The Rockefeller University Press 1968-01-31 /pmc/articles/PMC2138442/ /pubmed/5635380 Text en Copyright © 1968 by The Rockefeller University Press 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 Möller, Göran REGULATION OF CELLULAR ANTIBODY SYNTHESIS : CELLULAR 7S PRODUCTION AND LONGEVITY OF 7S ANTIGEN-SENSITIVE CELLS IN THE ABSENCE OF ANTIBODY FEEDBACK |
title | REGULATION OF CELLULAR ANTIBODY SYNTHESIS : CELLULAR 7S PRODUCTION AND LONGEVITY OF 7S ANTIGEN-SENSITIVE CELLS IN THE ABSENCE OF ANTIBODY FEEDBACK |
title_full | REGULATION OF CELLULAR ANTIBODY SYNTHESIS : CELLULAR 7S PRODUCTION AND LONGEVITY OF 7S ANTIGEN-SENSITIVE CELLS IN THE ABSENCE OF ANTIBODY FEEDBACK |
title_fullStr | REGULATION OF CELLULAR ANTIBODY SYNTHESIS : CELLULAR 7S PRODUCTION AND LONGEVITY OF 7S ANTIGEN-SENSITIVE CELLS IN THE ABSENCE OF ANTIBODY FEEDBACK |
title_full_unstemmed | REGULATION OF CELLULAR ANTIBODY SYNTHESIS : CELLULAR 7S PRODUCTION AND LONGEVITY OF 7S ANTIGEN-SENSITIVE CELLS IN THE ABSENCE OF ANTIBODY FEEDBACK |
title_short | REGULATION OF CELLULAR ANTIBODY SYNTHESIS : CELLULAR 7S PRODUCTION AND LONGEVITY OF 7S ANTIGEN-SENSITIVE CELLS IN THE ABSENCE OF ANTIBODY FEEDBACK |
title_sort | regulation of cellular antibody synthesis : cellular 7s production and longevity of 7s antigen-sensitive cells in the absence of antibody feedback |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2138442/ https://www.ncbi.nlm.nih.gov/pubmed/5635380 |
work_keys_str_mv | AT mollergoran regulationofcellularantibodysynthesiscellular7sproductionandlongevityof7santigensensitivecellsintheabsenceofantibodyfeedback |