Cargando…
DNA Repair Cofactors ATMIN and NBS1 Are Required to Suppress T Cell Activation
Proper development of the immune system is an intricate process dependent on many factors, including an intact DNA damage response. The DNA double-strand break signaling kinase ATM and its cofactor NBS1 are required during T cell development and for the maintenance of genomic stability. The role of...
Autores principales: | , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4636180/ https://www.ncbi.nlm.nih.gov/pubmed/26544571 http://dx.doi.org/10.1371/journal.pgen.1005645 |
_version_ | 1782399613670522880 |
---|---|
author | Prochazkova, Jana Sakaguchi, Shinya Owusu, Michel Mazouzi, Abdelghani Wiedner, Marc Velimezi, Georgia Moder, Martin Turchinovich, Gleb Hladik, Anastasiya Gurnhofer, Elisabeth Hayday, Adrian Behrens, Axel Knapp, Sylvia Kenner, Lukas Ellmeier, Wilfried Loizou, Joanna I. |
author_facet | Prochazkova, Jana Sakaguchi, Shinya Owusu, Michel Mazouzi, Abdelghani Wiedner, Marc Velimezi, Georgia Moder, Martin Turchinovich, Gleb Hladik, Anastasiya Gurnhofer, Elisabeth Hayday, Adrian Behrens, Axel Knapp, Sylvia Kenner, Lukas Ellmeier, Wilfried Loizou, Joanna I. |
author_sort | Prochazkova, Jana |
collection | PubMed |
description | Proper development of the immune system is an intricate process dependent on many factors, including an intact DNA damage response. The DNA double-strand break signaling kinase ATM and its cofactor NBS1 are required during T cell development and for the maintenance of genomic stability. The role of a second ATM cofactor, ATMIN (also known as ASCIZ) in T cells is much less clear, and whether ATMIN and NBS1 function in synergy in T cells is unknown. Here, we investigate the roles of ATMIN and NBS1, either alone or in combination, using murine models. We show loss of NBS1 led to a developmental block at the double-positive stage of T cell development, as well as reduced TCRα recombination, that was unexpectedly neither exacerbated nor alleviated by concomitant loss of ATMIN. In contrast, loss of both ATMIN and NBS1 enhanced DNA damage that drove spontaneous peripheral T cell hyperactivation, proliferation as well as excessive production of proinflammatory cytokines and chemokines, leading to a highly inflammatory environment. Intriguingly, the disease causing T cells were largely proficient for both ATMIN and NBS1. In vivo this resulted in severe intestinal inflammation, colitis and premature death. Our findings reveal a novel model for an intestinal bowel disease phenotype that occurs upon combined loss of the DNA repair cofactors ATMIN and NBS1. |
format | Online Article Text |
id | pubmed-4636180 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-46361802015-11-13 DNA Repair Cofactors ATMIN and NBS1 Are Required to Suppress T Cell Activation Prochazkova, Jana Sakaguchi, Shinya Owusu, Michel Mazouzi, Abdelghani Wiedner, Marc Velimezi, Georgia Moder, Martin Turchinovich, Gleb Hladik, Anastasiya Gurnhofer, Elisabeth Hayday, Adrian Behrens, Axel Knapp, Sylvia Kenner, Lukas Ellmeier, Wilfried Loizou, Joanna I. PLoS Genet Research Article Proper development of the immune system is an intricate process dependent on many factors, including an intact DNA damage response. The DNA double-strand break signaling kinase ATM and its cofactor NBS1 are required during T cell development and for the maintenance of genomic stability. The role of a second ATM cofactor, ATMIN (also known as ASCIZ) in T cells is much less clear, and whether ATMIN and NBS1 function in synergy in T cells is unknown. Here, we investigate the roles of ATMIN and NBS1, either alone or in combination, using murine models. We show loss of NBS1 led to a developmental block at the double-positive stage of T cell development, as well as reduced TCRα recombination, that was unexpectedly neither exacerbated nor alleviated by concomitant loss of ATMIN. In contrast, loss of both ATMIN and NBS1 enhanced DNA damage that drove spontaneous peripheral T cell hyperactivation, proliferation as well as excessive production of proinflammatory cytokines and chemokines, leading to a highly inflammatory environment. Intriguingly, the disease causing T cells were largely proficient for both ATMIN and NBS1. In vivo this resulted in severe intestinal inflammation, colitis and premature death. Our findings reveal a novel model for an intestinal bowel disease phenotype that occurs upon combined loss of the DNA repair cofactors ATMIN and NBS1. Public Library of Science 2015-11-06 /pmc/articles/PMC4636180/ /pubmed/26544571 http://dx.doi.org/10.1371/journal.pgen.1005645 Text en © 2015 Prochazkova et al 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 Prochazkova, Jana Sakaguchi, Shinya Owusu, Michel Mazouzi, Abdelghani Wiedner, Marc Velimezi, Georgia Moder, Martin Turchinovich, Gleb Hladik, Anastasiya Gurnhofer, Elisabeth Hayday, Adrian Behrens, Axel Knapp, Sylvia Kenner, Lukas Ellmeier, Wilfried Loizou, Joanna I. DNA Repair Cofactors ATMIN and NBS1 Are Required to Suppress T Cell Activation |
title | DNA Repair Cofactors ATMIN and NBS1 Are Required to Suppress T Cell Activation |
title_full | DNA Repair Cofactors ATMIN and NBS1 Are Required to Suppress T Cell Activation |
title_fullStr | DNA Repair Cofactors ATMIN and NBS1 Are Required to Suppress T Cell Activation |
title_full_unstemmed | DNA Repair Cofactors ATMIN and NBS1 Are Required to Suppress T Cell Activation |
title_short | DNA Repair Cofactors ATMIN and NBS1 Are Required to Suppress T Cell Activation |
title_sort | dna repair cofactors atmin and nbs1 are required to suppress t cell activation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4636180/ https://www.ncbi.nlm.nih.gov/pubmed/26544571 http://dx.doi.org/10.1371/journal.pgen.1005645 |
work_keys_str_mv | AT prochazkovajana dnarepaircofactorsatminandnbs1arerequiredtosuppresstcellactivation AT sakaguchishinya dnarepaircofactorsatminandnbs1arerequiredtosuppresstcellactivation AT owusumichel dnarepaircofactorsatminandnbs1arerequiredtosuppresstcellactivation AT mazouziabdelghani dnarepaircofactorsatminandnbs1arerequiredtosuppresstcellactivation AT wiednermarc dnarepaircofactorsatminandnbs1arerequiredtosuppresstcellactivation AT velimezigeorgia dnarepaircofactorsatminandnbs1arerequiredtosuppresstcellactivation AT modermartin dnarepaircofactorsatminandnbs1arerequiredtosuppresstcellactivation AT turchinovichgleb dnarepaircofactorsatminandnbs1arerequiredtosuppresstcellactivation AT hladikanastasiya dnarepaircofactorsatminandnbs1arerequiredtosuppresstcellactivation AT gurnhoferelisabeth dnarepaircofactorsatminandnbs1arerequiredtosuppresstcellactivation AT haydayadrian dnarepaircofactorsatminandnbs1arerequiredtosuppresstcellactivation AT behrensaxel dnarepaircofactorsatminandnbs1arerequiredtosuppresstcellactivation AT knappsylvia dnarepaircofactorsatminandnbs1arerequiredtosuppresstcellactivation AT kennerlukas dnarepaircofactorsatminandnbs1arerequiredtosuppresstcellactivation AT ellmeierwilfried dnarepaircofactorsatminandnbs1arerequiredtosuppresstcellactivation AT loizoujoannai dnarepaircofactorsatminandnbs1arerequiredtosuppresstcellactivation |