Cargando…
Germinal center B cell development has distinctly regulated stages completed by disengagement from T cell help
To reconcile conflicting reports on the role of CD40 signaling in germinal center (GC) formation, we examined the earliest stages of murine GC B cell differentiation. Peri-follicular GC precursors first expressed intermediate levels of BCL6 while co-expressing the transcription factors RelB and IRF4...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5429091/ https://www.ncbi.nlm.nih.gov/pubmed/28498098 http://dx.doi.org/10.7554/eLife.19552 |
_version_ | 1783235959864688640 |
---|---|
author | Zhang, Ting-ting Gonzalez, David G Cote, Christine M Kerfoot, Steven M Deng, Shaoli Cheng, Yuqing Magari, Masaki Haberman, Ann M |
author_facet | Zhang, Ting-ting Gonzalez, David G Cote, Christine M Kerfoot, Steven M Deng, Shaoli Cheng, Yuqing Magari, Masaki Haberman, Ann M |
author_sort | Zhang, Ting-ting |
collection | PubMed |
description | To reconcile conflicting reports on the role of CD40 signaling in germinal center (GC) formation, we examined the earliest stages of murine GC B cell differentiation. Peri-follicular GC precursors first expressed intermediate levels of BCL6 while co-expressing the transcription factors RelB and IRF4, the latter known to repress Bcl6 transcription. Transition of GC precursors to the BCL6(hi) follicular state was associated with cell division, although the number of required cell divisions was immunogen dose dependent. Potentiating T cell help or CD40 signaling in these GC precursors actively repressed GC B cell maturation and diverted their fate towards plasmablast differentiation, whereas depletion of CD4+ T cells promoted this initial transition. Thus while CD40 signaling in B cells is necessary to generate the immediate precursors of GC B cells, transition to the BCL6(hi) follicular state is promoted by a regional and transient diminution of T cell help. DOI: http://dx.doi.org/10.7554/eLife.19552.001 |
format | Online Article Text |
id | pubmed-5429091 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-54290912017-05-15 Germinal center B cell development has distinctly regulated stages completed by disengagement from T cell help Zhang, Ting-ting Gonzalez, David G Cote, Christine M Kerfoot, Steven M Deng, Shaoli Cheng, Yuqing Magari, Masaki Haberman, Ann M eLife Immunology To reconcile conflicting reports on the role of CD40 signaling in germinal center (GC) formation, we examined the earliest stages of murine GC B cell differentiation. Peri-follicular GC precursors first expressed intermediate levels of BCL6 while co-expressing the transcription factors RelB and IRF4, the latter known to repress Bcl6 transcription. Transition of GC precursors to the BCL6(hi) follicular state was associated with cell division, although the number of required cell divisions was immunogen dose dependent. Potentiating T cell help or CD40 signaling in these GC precursors actively repressed GC B cell maturation and diverted their fate towards plasmablast differentiation, whereas depletion of CD4+ T cells promoted this initial transition. Thus while CD40 signaling in B cells is necessary to generate the immediate precursors of GC B cells, transition to the BCL6(hi) follicular state is promoted by a regional and transient diminution of T cell help. DOI: http://dx.doi.org/10.7554/eLife.19552.001 eLife Sciences Publications, Ltd 2017-05-12 /pmc/articles/PMC5429091/ /pubmed/28498098 http://dx.doi.org/10.7554/eLife.19552 Text en © 2017, Zhang et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Immunology Zhang, Ting-ting Gonzalez, David G Cote, Christine M Kerfoot, Steven M Deng, Shaoli Cheng, Yuqing Magari, Masaki Haberman, Ann M Germinal center B cell development has distinctly regulated stages completed by disengagement from T cell help |
title | Germinal center B cell development has distinctly regulated stages completed by disengagement from T cell help |
title_full | Germinal center B cell development has distinctly regulated stages completed by disengagement from T cell help |
title_fullStr | Germinal center B cell development has distinctly regulated stages completed by disengagement from T cell help |
title_full_unstemmed | Germinal center B cell development has distinctly regulated stages completed by disengagement from T cell help |
title_short | Germinal center B cell development has distinctly regulated stages completed by disengagement from T cell help |
title_sort | germinal center b cell development has distinctly regulated stages completed by disengagement from t cell help |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5429091/ https://www.ncbi.nlm.nih.gov/pubmed/28498098 http://dx.doi.org/10.7554/eLife.19552 |
work_keys_str_mv | AT zhangtingting germinalcenterbcelldevelopmenthasdistinctlyregulatedstagescompletedbydisengagementfromtcellhelp AT gonzalezdavidg germinalcenterbcelldevelopmenthasdistinctlyregulatedstagescompletedbydisengagementfromtcellhelp AT cotechristinem germinalcenterbcelldevelopmenthasdistinctlyregulatedstagescompletedbydisengagementfromtcellhelp AT kerfootstevenm germinalcenterbcelldevelopmenthasdistinctlyregulatedstagescompletedbydisengagementfromtcellhelp AT dengshaoli germinalcenterbcelldevelopmenthasdistinctlyregulatedstagescompletedbydisengagementfromtcellhelp AT chengyuqing germinalcenterbcelldevelopmenthasdistinctlyregulatedstagescompletedbydisengagementfromtcellhelp AT magarimasaki germinalcenterbcelldevelopmenthasdistinctlyregulatedstagescompletedbydisengagementfromtcellhelp AT habermanannm germinalcenterbcelldevelopmenthasdistinctlyregulatedstagescompletedbydisengagementfromtcellhelp |