Cargando…
Calcineurin/NFAT signaling and innate host defence: a role for NOD1-mediated phagocytic functions
The calcineurin/nuclear factor of activated T cells (NFATs) signaling pathway plays a central role in T cell mediated adaptive immune responses, but a number of recent studies demonstrated that calcineurin/NFAT signaling also plays a key role in the control of the innate immune response by myeloid c...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3910266/ https://www.ncbi.nlm.nih.gov/pubmed/24479879 http://dx.doi.org/10.1186/1478-811X-12-8 |
_version_ | 1782301957063442432 |
---|---|
author | Vandewalle, Alain Tourneur, Emilie Bens, Marcelle Chassin, Cécilia Werts, Catherine |
author_facet | Vandewalle, Alain Tourneur, Emilie Bens, Marcelle Chassin, Cécilia Werts, Catherine |
author_sort | Vandewalle, Alain |
collection | PubMed |
description | The calcineurin/nuclear factor of activated T cells (NFATs) signaling pathway plays a central role in T cell mediated adaptive immune responses, but a number of recent studies demonstrated that calcineurin/NFAT signaling also plays a key role in the control of the innate immune response by myeloid cells. Calcineurin inhibitors, such as cyclosporine A (CsA) and tacrolimus (FK506), are commonly used in organ transplantation to prevent graft rejection and in a variety of immune diseases. These immunosuppressive drugs have adverse effects and significantly increase host’s susceptibility towards bacterial or fungal infections. Recent studies highlighted the role of NFAT signaling in fungal infection and in the control of the pattern recognition receptor nucleotide-binding oligomerization domain-containing protein 1 (NOD1), which predominantly senses invasive Gram-negative bacteria and mediates neutrophil phagocytic functions. This review summarises some of the current knowledge concerning the role of NFAT signaling in the innate immune response and the recent advances on NFAT-dependent inhibition of NOD1-mediated innate immune response caused by CsA, which may contribute to sensitizing transplant recipients to bacterial infection. |
format | Online Article Text |
id | pubmed-3910266 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39102662014-02-04 Calcineurin/NFAT signaling and innate host defence: a role for NOD1-mediated phagocytic functions Vandewalle, Alain Tourneur, Emilie Bens, Marcelle Chassin, Cécilia Werts, Catherine Cell Commun Signal Review The calcineurin/nuclear factor of activated T cells (NFATs) signaling pathway plays a central role in T cell mediated adaptive immune responses, but a number of recent studies demonstrated that calcineurin/NFAT signaling also plays a key role in the control of the innate immune response by myeloid cells. Calcineurin inhibitors, such as cyclosporine A (CsA) and tacrolimus (FK506), are commonly used in organ transplantation to prevent graft rejection and in a variety of immune diseases. These immunosuppressive drugs have adverse effects and significantly increase host’s susceptibility towards bacterial or fungal infections. Recent studies highlighted the role of NFAT signaling in fungal infection and in the control of the pattern recognition receptor nucleotide-binding oligomerization domain-containing protein 1 (NOD1), which predominantly senses invasive Gram-negative bacteria and mediates neutrophil phagocytic functions. This review summarises some of the current knowledge concerning the role of NFAT signaling in the innate immune response and the recent advances on NFAT-dependent inhibition of NOD1-mediated innate immune response caused by CsA, which may contribute to sensitizing transplant recipients to bacterial infection. BioMed Central 2014-01-30 /pmc/articles/PMC3910266/ /pubmed/24479879 http://dx.doi.org/10.1186/1478-811X-12-8 Text en Copyright © 2014 Vandewalle et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Vandewalle, Alain Tourneur, Emilie Bens, Marcelle Chassin, Cécilia Werts, Catherine Calcineurin/NFAT signaling and innate host defence: a role for NOD1-mediated phagocytic functions |
title | Calcineurin/NFAT signaling and innate host defence: a role for NOD1-mediated phagocytic functions |
title_full | Calcineurin/NFAT signaling and innate host defence: a role for NOD1-mediated phagocytic functions |
title_fullStr | Calcineurin/NFAT signaling and innate host defence: a role for NOD1-mediated phagocytic functions |
title_full_unstemmed | Calcineurin/NFAT signaling and innate host defence: a role for NOD1-mediated phagocytic functions |
title_short | Calcineurin/NFAT signaling and innate host defence: a role for NOD1-mediated phagocytic functions |
title_sort | calcineurin/nfat signaling and innate host defence: a role for nod1-mediated phagocytic functions |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3910266/ https://www.ncbi.nlm.nih.gov/pubmed/24479879 http://dx.doi.org/10.1186/1478-811X-12-8 |
work_keys_str_mv | AT vandewallealain calcineurinnfatsignalingandinnatehostdefencearolefornod1mediatedphagocyticfunctions AT tourneuremilie calcineurinnfatsignalingandinnatehostdefencearolefornod1mediatedphagocyticfunctions AT bensmarcelle calcineurinnfatsignalingandinnatehostdefencearolefornod1mediatedphagocyticfunctions AT chassincecilia calcineurinnfatsignalingandinnatehostdefencearolefornod1mediatedphagocyticfunctions AT wertscatherine calcineurinnfatsignalingandinnatehostdefencearolefornod1mediatedphagocyticfunctions |