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The BiP Cochaperone ERdj4 Is Required for B Cell Development and Function

ERdj4 is a BiP cochaperone regulated by the unfolded protein response to facilitate degradation of unfolded and/or misfolded proteins in the endoplasmic reticulum. As the unfolded protein response plays a critical role in B cell maturation and antibody production, ERdj4 gene trap mice were generated...

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Autores principales: Fritz, Jill M., Weaver, Timothy E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4164662/
https://www.ncbi.nlm.nih.gov/pubmed/25222125
http://dx.doi.org/10.1371/journal.pone.0107473
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author Fritz, Jill M.
Weaver, Timothy E.
author_facet Fritz, Jill M.
Weaver, Timothy E.
author_sort Fritz, Jill M.
collection PubMed
description ERdj4 is a BiP cochaperone regulated by the unfolded protein response to facilitate degradation of unfolded and/or misfolded proteins in the endoplasmic reticulum. As the unfolded protein response plays a critical role in B cell maturation and antibody production, ERdj4 gene trap mice were generated to determine if this chaperone was required for B cell homeostasis. Homozygosity for the trapped allele resulted in hypomorphic expression of ERdj4 in bone marrow cells and abnormal development of hematopoietic lineages in the bone marrow. The number of myeloid cells was increased, while the number of erythroid and B lymphoid cells was reduced in ERdj4 gene trap mice compared to controls. An intrinsic B cell defect was identified that decreased survival of B cell precursors including large and small pre-B, and immature B cells. Consistent with impaired B lymphopoiesis, the number of mature follicular B cells was reduced in both the bone marrow and spleen of ERdj4 gene trap mice. Paradoxically, unchallenged ERdj4 gene trap mice showed non-specific hypergammaglobulinemia and gene trap B cells exhibited increased proliferation, survival and isotype switching in response to LPS stimulation. Although ERdj4 gene trap mice responded normally to T cell-independent antigen, they failed to mount a specific antibody response to T cell-dependent antigen in vivo. Collectively, these findings demonstrate that the chaperone activity of ERdj4 is required for survival of B cell progenitors and normal antibody production.
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spelling pubmed-41646622014-09-19 The BiP Cochaperone ERdj4 Is Required for B Cell Development and Function Fritz, Jill M. Weaver, Timothy E. PLoS One Research Article ERdj4 is a BiP cochaperone regulated by the unfolded protein response to facilitate degradation of unfolded and/or misfolded proteins in the endoplasmic reticulum. As the unfolded protein response plays a critical role in B cell maturation and antibody production, ERdj4 gene trap mice were generated to determine if this chaperone was required for B cell homeostasis. Homozygosity for the trapped allele resulted in hypomorphic expression of ERdj4 in bone marrow cells and abnormal development of hematopoietic lineages in the bone marrow. The number of myeloid cells was increased, while the number of erythroid and B lymphoid cells was reduced in ERdj4 gene trap mice compared to controls. An intrinsic B cell defect was identified that decreased survival of B cell precursors including large and small pre-B, and immature B cells. Consistent with impaired B lymphopoiesis, the number of mature follicular B cells was reduced in both the bone marrow and spleen of ERdj4 gene trap mice. Paradoxically, unchallenged ERdj4 gene trap mice showed non-specific hypergammaglobulinemia and gene trap B cells exhibited increased proliferation, survival and isotype switching in response to LPS stimulation. Although ERdj4 gene trap mice responded normally to T cell-independent antigen, they failed to mount a specific antibody response to T cell-dependent antigen in vivo. Collectively, these findings demonstrate that the chaperone activity of ERdj4 is required for survival of B cell progenitors and normal antibody production. Public Library of Science 2014-09-15 /pmc/articles/PMC4164662/ /pubmed/25222125 http://dx.doi.org/10.1371/journal.pone.0107473 Text en © 2014 Fritz, Weaver http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Fritz, Jill M.
Weaver, Timothy E.
The BiP Cochaperone ERdj4 Is Required for B Cell Development and Function
title The BiP Cochaperone ERdj4 Is Required for B Cell Development and Function
title_full The BiP Cochaperone ERdj4 Is Required for B Cell Development and Function
title_fullStr The BiP Cochaperone ERdj4 Is Required for B Cell Development and Function
title_full_unstemmed The BiP Cochaperone ERdj4 Is Required for B Cell Development and Function
title_short The BiP Cochaperone ERdj4 Is Required for B Cell Development and Function
title_sort bip cochaperone erdj4 is required for b cell development and function
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4164662/
https://www.ncbi.nlm.nih.gov/pubmed/25222125
http://dx.doi.org/10.1371/journal.pone.0107473
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