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PDGFA-associated protein 1 protects mature B lymphocytes from stress-induced cell death and promotes antibody gene diversification
The establishment of protective humoral immunity is dependent on the ability of mature B cells to undergo antibody gene diversification while adjusting to the physiological stressors induced by activation with the antigen. Mature B cells diversify their antibody genes by class switch recombination (...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7537392/ https://www.ncbi.nlm.nih.gov/pubmed/32609329 http://dx.doi.org/10.1084/jem.20200137 |
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author | Delgado-Benito, Verónica Berruezo-Llacuna, Maria Altwasser, Robert Winkler, Wiebke Sundaravinayagam, Devakumar Balasubramanian, Sandhya Caganova, Marieta Graf, Robin Rahjouei, Ali Henke, Marie-Thérèse Driesner, Madlen Keller, Lisa Prigione, Alessandro Janz, Martin Akalin, Altuna Di Virgilio, Michela |
author_facet | Delgado-Benito, Verónica Berruezo-Llacuna, Maria Altwasser, Robert Winkler, Wiebke Sundaravinayagam, Devakumar Balasubramanian, Sandhya Caganova, Marieta Graf, Robin Rahjouei, Ali Henke, Marie-Thérèse Driesner, Madlen Keller, Lisa Prigione, Alessandro Janz, Martin Akalin, Altuna Di Virgilio, Michela |
author_sort | Delgado-Benito, Verónica |
collection | PubMed |
description | The establishment of protective humoral immunity is dependent on the ability of mature B cells to undergo antibody gene diversification while adjusting to the physiological stressors induced by activation with the antigen. Mature B cells diversify their antibody genes by class switch recombination (CSR) and somatic hypermutation (SHM), which are both dependent on efficient induction of activation-induced cytidine deaminase (AID). Here, we identified PDGFA-associated protein 1 (Pdap1) as an essential regulator of cellular homeostasis in mature B cells. Pdap1 deficiency leads to sustained expression of the integrated stress response (ISR) effector activating transcription factor 4 (Atf4) and induction of the ISR transcriptional program, increased cell death, and defective AID expression. As a consequence, loss of Pdap1 reduces germinal center B cell formation and impairs CSR and SHM. Thus, Pdap1 protects mature B cells against chronic ISR activation and ensures efficient antibody diversification by promoting their survival and optimal function. |
format | Online Article Text |
id | pubmed-7537392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-75373922020-10-14 PDGFA-associated protein 1 protects mature B lymphocytes from stress-induced cell death and promotes antibody gene diversification Delgado-Benito, Verónica Berruezo-Llacuna, Maria Altwasser, Robert Winkler, Wiebke Sundaravinayagam, Devakumar Balasubramanian, Sandhya Caganova, Marieta Graf, Robin Rahjouei, Ali Henke, Marie-Thérèse Driesner, Madlen Keller, Lisa Prigione, Alessandro Janz, Martin Akalin, Altuna Di Virgilio, Michela J Exp Med Article The establishment of protective humoral immunity is dependent on the ability of mature B cells to undergo antibody gene diversification while adjusting to the physiological stressors induced by activation with the antigen. Mature B cells diversify their antibody genes by class switch recombination (CSR) and somatic hypermutation (SHM), which are both dependent on efficient induction of activation-induced cytidine deaminase (AID). Here, we identified PDGFA-associated protein 1 (Pdap1) as an essential regulator of cellular homeostasis in mature B cells. Pdap1 deficiency leads to sustained expression of the integrated stress response (ISR) effector activating transcription factor 4 (Atf4) and induction of the ISR transcriptional program, increased cell death, and defective AID expression. As a consequence, loss of Pdap1 reduces germinal center B cell formation and impairs CSR and SHM. Thus, Pdap1 protects mature B cells against chronic ISR activation and ensures efficient antibody diversification by promoting their survival and optimal function. Rockefeller University Press 2020-07-01 /pmc/articles/PMC7537392/ /pubmed/32609329 http://dx.doi.org/10.1084/jem.20200137 Text en © 2020 Delgado-Benito et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Delgado-Benito, Verónica Berruezo-Llacuna, Maria Altwasser, Robert Winkler, Wiebke Sundaravinayagam, Devakumar Balasubramanian, Sandhya Caganova, Marieta Graf, Robin Rahjouei, Ali Henke, Marie-Thérèse Driesner, Madlen Keller, Lisa Prigione, Alessandro Janz, Martin Akalin, Altuna Di Virgilio, Michela PDGFA-associated protein 1 protects mature B lymphocytes from stress-induced cell death and promotes antibody gene diversification |
title | PDGFA-associated protein 1 protects mature B lymphocytes from stress-induced cell death and promotes antibody gene diversification |
title_full | PDGFA-associated protein 1 protects mature B lymphocytes from stress-induced cell death and promotes antibody gene diversification |
title_fullStr | PDGFA-associated protein 1 protects mature B lymphocytes from stress-induced cell death and promotes antibody gene diversification |
title_full_unstemmed | PDGFA-associated protein 1 protects mature B lymphocytes from stress-induced cell death and promotes antibody gene diversification |
title_short | PDGFA-associated protein 1 protects mature B lymphocytes from stress-induced cell death and promotes antibody gene diversification |
title_sort | pdgfa-associated protein 1 protects mature b lymphocytes from stress-induced cell death and promotes antibody gene diversification |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7537392/ https://www.ncbi.nlm.nih.gov/pubmed/32609329 http://dx.doi.org/10.1084/jem.20200137 |
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