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A mechanism of T cell dependent selection of antigen engaged Germinal Center B cells
A model of B cell affinity selection is proposed, and an explanation of peripheral tolerance mechanisms through antibody repertoire editing is presented. We show that affinity discrimination between B cells is driven by a competition between obtaining T cell help and removal of B cells from the ligh...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107130/ https://www.ncbi.nlm.nih.gov/pubmed/30138347 http://dx.doi.org/10.1371/journal.pone.0200241 |
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author | Krishna, Vinod Bachman, Kurtis E. |
author_facet | Krishna, Vinod Bachman, Kurtis E. |
author_sort | Krishna, Vinod |
collection | PubMed |
description | A model of B cell affinity selection is proposed, and an explanation of peripheral tolerance mechanisms through antibody repertoire editing is presented. We show that affinity discrimination between B cells is driven by a competition between obtaining T cell help and removal of B cells from the light zone, either through apoptosis or by a return to the dark zone of germinal centers. We demonstrate that this mechanism also allows for the negative selection of self reactive B cells and maintenance of B cell tolerance during the Germinal Center reaction. Finally, we demonstrate that clonal expansion upon return to the Germinal Center dark zone amplifies differences in the antigen affinity of B cells that survive the light zone. |
format | Online Article Text |
id | pubmed-6107130 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-61071302018-08-30 A mechanism of T cell dependent selection of antigen engaged Germinal Center B cells Krishna, Vinod Bachman, Kurtis E. PLoS One Research Article A model of B cell affinity selection is proposed, and an explanation of peripheral tolerance mechanisms through antibody repertoire editing is presented. We show that affinity discrimination between B cells is driven by a competition between obtaining T cell help and removal of B cells from the light zone, either through apoptosis or by a return to the dark zone of germinal centers. We demonstrate that this mechanism also allows for the negative selection of self reactive B cells and maintenance of B cell tolerance during the Germinal Center reaction. Finally, we demonstrate that clonal expansion upon return to the Germinal Center dark zone amplifies differences in the antigen affinity of B cells that survive the light zone. Public Library of Science 2018-08-23 /pmc/articles/PMC6107130/ /pubmed/30138347 http://dx.doi.org/10.1371/journal.pone.0200241 Text en © 2018 Krishna, Bachman http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Krishna, Vinod Bachman, Kurtis E. A mechanism of T cell dependent selection of antigen engaged Germinal Center B cells |
title | A mechanism of T cell dependent selection of antigen engaged Germinal Center B cells |
title_full | A mechanism of T cell dependent selection of antigen engaged Germinal Center B cells |
title_fullStr | A mechanism of T cell dependent selection of antigen engaged Germinal Center B cells |
title_full_unstemmed | A mechanism of T cell dependent selection of antigen engaged Germinal Center B cells |
title_short | A mechanism of T cell dependent selection of antigen engaged Germinal Center B cells |
title_sort | mechanism of t cell dependent selection of antigen engaged germinal center b cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107130/ https://www.ncbi.nlm.nih.gov/pubmed/30138347 http://dx.doi.org/10.1371/journal.pone.0200241 |
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