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c-MYC is required for germinal center selection and cyclic re-entry

Upon antigenic challenge, B cells enter the dark-zone (DZ) of germinal-centers (GC) to proliferate and hypermutate their immunoglobulin genes. Mutants with increased affinity are positively selected in the light-zone (LZ) to either differentiate into plasma and memory cells, or re-enter the DZ. The...

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Detalles Bibliográficos
Autores principales: Dominguez-Sola, David, Victora, Gabriel D., Ying, Carol Y., Phan, Ryan T., Saito, Masumichi, Nussenzweig, Michel C., Dalla-Favera, Riccardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3711534/
https://www.ncbi.nlm.nih.gov/pubmed/23001145
http://dx.doi.org/10.1038/ni.2428
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author Dominguez-Sola, David
Victora, Gabriel D.
Ying, Carol Y.
Phan, Ryan T.
Saito, Masumichi
Nussenzweig, Michel C.
Dalla-Favera, Riccardo
author_facet Dominguez-Sola, David
Victora, Gabriel D.
Ying, Carol Y.
Phan, Ryan T.
Saito, Masumichi
Nussenzweig, Michel C.
Dalla-Favera, Riccardo
author_sort Dominguez-Sola, David
collection PubMed
description Upon antigenic challenge, B cells enter the dark-zone (DZ) of germinal-centers (GC) to proliferate and hypermutate their immunoglobulin genes. Mutants with increased affinity are positively selected in the light-zone (LZ) to either differentiate into plasma and memory cells, or re-enter the DZ. The molecular circuits governing GC positive selection are not known. We show that the GC reaction requires the biphasic regulation of c-MYC expression, involving its transient induction during early GC commitment, its repression by BCL6 in DZ B cells, and its re-induction in B cells selected for DZ re-entry. Inhibition of MYC in vivo leads to GC collapse, indicating an essential role in GCs. These results have implications for the mechanism of GC selection and the role of MYC in lymphomagenesis.
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spelling pubmed-37115342013-07-15 c-MYC is required for germinal center selection and cyclic re-entry Dominguez-Sola, David Victora, Gabriel D. Ying, Carol Y. Phan, Ryan T. Saito, Masumichi Nussenzweig, Michel C. Dalla-Favera, Riccardo Nat Immunol Article Upon antigenic challenge, B cells enter the dark-zone (DZ) of germinal-centers (GC) to proliferate and hypermutate their immunoglobulin genes. Mutants with increased affinity are positively selected in the light-zone (LZ) to either differentiate into plasma and memory cells, or re-enter the DZ. The molecular circuits governing GC positive selection are not known. We show that the GC reaction requires the biphasic regulation of c-MYC expression, involving its transient induction during early GC commitment, its repression by BCL6 in DZ B cells, and its re-induction in B cells selected for DZ re-entry. Inhibition of MYC in vivo leads to GC collapse, indicating an essential role in GCs. These results have implications for the mechanism of GC selection and the role of MYC in lymphomagenesis. 2012-09-23 2012-11 /pmc/articles/PMC3711534/ /pubmed/23001145 http://dx.doi.org/10.1038/ni.2428 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Dominguez-Sola, David
Victora, Gabriel D.
Ying, Carol Y.
Phan, Ryan T.
Saito, Masumichi
Nussenzweig, Michel C.
Dalla-Favera, Riccardo
c-MYC is required for germinal center selection and cyclic re-entry
title c-MYC is required for germinal center selection and cyclic re-entry
title_full c-MYC is required for germinal center selection and cyclic re-entry
title_fullStr c-MYC is required for germinal center selection and cyclic re-entry
title_full_unstemmed c-MYC is required for germinal center selection and cyclic re-entry
title_short c-MYC is required for germinal center selection and cyclic re-entry
title_sort c-myc is required for germinal center selection and cyclic re-entry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3711534/
https://www.ncbi.nlm.nih.gov/pubmed/23001145
http://dx.doi.org/10.1038/ni.2428
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