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Congenital Defects in Actin Dynamics of Germinal Center B Cells

The germinal center (GC) is a transient anatomical structure formed during the adaptive immune response that leads to antibody affinity maturation and serological memory. Recent works using two-photon microscopy reveals that the GC is a highly dynamic structure and GC B cells are highly motile. An e...

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Detalles Bibliográficos
Autores principales: He, Minghui, Westerberg, Lisa S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6414452/
https://www.ncbi.nlm.nih.gov/pubmed/30894852
http://dx.doi.org/10.3389/fimmu.2019.00296
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author He, Minghui
Westerberg, Lisa S.
author_facet He, Minghui
Westerberg, Lisa S.
author_sort He, Minghui
collection PubMed
description The germinal center (GC) is a transient anatomical structure formed during the adaptive immune response that leads to antibody affinity maturation and serological memory. Recent works using two-photon microscopy reveals that the GC is a highly dynamic structure and GC B cells are highly motile. An efficient selection of high affinity B cells clones within the GC crucially relies on the interplay of proliferation, genome editing, cell-cell interaction, and migration. All these processes require actin cytoskeleton rearrangement to be well-coordinated. Dysregulated actin dynamics may impede on multiple stages during B cell affinity maturation, which could lead to aberrant GC response and result in autoimmunity and B cell malignancy. This review mainly focuses on the recent works that investigate the role of actin regulators during the GC response.
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spelling pubmed-64144522019-03-20 Congenital Defects in Actin Dynamics of Germinal Center B Cells He, Minghui Westerberg, Lisa S. Front Immunol Immunology The germinal center (GC) is a transient anatomical structure formed during the adaptive immune response that leads to antibody affinity maturation and serological memory. Recent works using two-photon microscopy reveals that the GC is a highly dynamic structure and GC B cells are highly motile. An efficient selection of high affinity B cells clones within the GC crucially relies on the interplay of proliferation, genome editing, cell-cell interaction, and migration. All these processes require actin cytoskeleton rearrangement to be well-coordinated. Dysregulated actin dynamics may impede on multiple stages during B cell affinity maturation, which could lead to aberrant GC response and result in autoimmunity and B cell malignancy. This review mainly focuses on the recent works that investigate the role of actin regulators during the GC response. Frontiers Media S.A. 2019-03-06 /pmc/articles/PMC6414452/ /pubmed/30894852 http://dx.doi.org/10.3389/fimmu.2019.00296 Text en Copyright © 2019 He and Westerberg. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
He, Minghui
Westerberg, Lisa S.
Congenital Defects in Actin Dynamics of Germinal Center B Cells
title Congenital Defects in Actin Dynamics of Germinal Center B Cells
title_full Congenital Defects in Actin Dynamics of Germinal Center B Cells
title_fullStr Congenital Defects in Actin Dynamics of Germinal Center B Cells
title_full_unstemmed Congenital Defects in Actin Dynamics of Germinal Center B Cells
title_short Congenital Defects in Actin Dynamics of Germinal Center B Cells
title_sort congenital defects in actin dynamics of germinal center b cells
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6414452/
https://www.ncbi.nlm.nih.gov/pubmed/30894852
http://dx.doi.org/10.3389/fimmu.2019.00296
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