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cGAS/STING/TBK1/IRF3 Signaling Pathway Activates BMDCs Maturation Following Mycobacterium bovis Infection

Cyclic GMP-AMP synthase (cGAS) is an important cytosolic DNA sensor that plays a crucial role in triggering STING-dependent signal and inducing type I interferons (IFNs). cGAS is important for intracellular bacterial recognition and innate immune responses. However, the regulating effect of the cGAS...

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Autores principales: Li, Qiang, Liu, Chunfa, Yue, Ruichao, El-Ashram, Saeed, Wang, Jie, He, Xiaoli, Zhao, Deming, Zhou, Xiangmei, Xu, Lihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6412216/
https://www.ncbi.nlm.nih.gov/pubmed/30791397
http://dx.doi.org/10.3390/ijms20040895
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author Li, Qiang
Liu, Chunfa
Yue, Ruichao
El-Ashram, Saeed
Wang, Jie
He, Xiaoli
Zhao, Deming
Zhou, Xiangmei
Xu, Lihua
author_facet Li, Qiang
Liu, Chunfa
Yue, Ruichao
El-Ashram, Saeed
Wang, Jie
He, Xiaoli
Zhao, Deming
Zhou, Xiangmei
Xu, Lihua
author_sort Li, Qiang
collection PubMed
description Cyclic GMP-AMP synthase (cGAS) is an important cytosolic DNA sensor that plays a crucial role in triggering STING-dependent signal and inducing type I interferons (IFNs). cGAS is important for intracellular bacterial recognition and innate immune responses. However, the regulating effect of the cGAS pathway for bone marrow-derived dendritic cells (BMDCs) during Mycobacterium bovis (M. bovis) infection is still unknown. We hypothesized that the maturation and activation of BMDCs were modulated by the cGAS/STING/TBK1/IRF3 signaling pathway. In this study, we found that M. bovis promoted phenotypic maturation and functional activation of BMDCs via the cGAS signaling pathway, with the type I IFN and its receptor (IFNAR) contributing. Additionally, we showed that the type I IFN pathway promoted CD4(+) T cells’ proliferation with BMDC during M. bovis infection. Meanwhile, the related cytokines increased the expression involved in this signaling pathway. These data highlight the mechanism of the cGAS and type I IFN pathway in regulating the maturation and activation of BMDCs, emphasizing the important role of this signaling pathway and BMDCs against M. bovis. This study provides new insight into the interaction between cGAS and dendritic cells (DCs), which could be considered in the development of new drugs and vaccines against tuberculosis.
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spelling pubmed-64122162019-04-05 cGAS/STING/TBK1/IRF3 Signaling Pathway Activates BMDCs Maturation Following Mycobacterium bovis Infection Li, Qiang Liu, Chunfa Yue, Ruichao El-Ashram, Saeed Wang, Jie He, Xiaoli Zhao, Deming Zhou, Xiangmei Xu, Lihua Int J Mol Sci Article Cyclic GMP-AMP synthase (cGAS) is an important cytosolic DNA sensor that plays a crucial role in triggering STING-dependent signal and inducing type I interferons (IFNs). cGAS is important for intracellular bacterial recognition and innate immune responses. However, the regulating effect of the cGAS pathway for bone marrow-derived dendritic cells (BMDCs) during Mycobacterium bovis (M. bovis) infection is still unknown. We hypothesized that the maturation and activation of BMDCs were modulated by the cGAS/STING/TBK1/IRF3 signaling pathway. In this study, we found that M. bovis promoted phenotypic maturation and functional activation of BMDCs via the cGAS signaling pathway, with the type I IFN and its receptor (IFNAR) contributing. Additionally, we showed that the type I IFN pathway promoted CD4(+) T cells’ proliferation with BMDC during M. bovis infection. Meanwhile, the related cytokines increased the expression involved in this signaling pathway. These data highlight the mechanism of the cGAS and type I IFN pathway in regulating the maturation and activation of BMDCs, emphasizing the important role of this signaling pathway and BMDCs against M. bovis. This study provides new insight into the interaction between cGAS and dendritic cells (DCs), which could be considered in the development of new drugs and vaccines against tuberculosis. MDPI 2019-02-19 /pmc/articles/PMC6412216/ /pubmed/30791397 http://dx.doi.org/10.3390/ijms20040895 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Li, Qiang
Liu, Chunfa
Yue, Ruichao
El-Ashram, Saeed
Wang, Jie
He, Xiaoli
Zhao, Deming
Zhou, Xiangmei
Xu, Lihua
cGAS/STING/TBK1/IRF3 Signaling Pathway Activates BMDCs Maturation Following Mycobacterium bovis Infection
title cGAS/STING/TBK1/IRF3 Signaling Pathway Activates BMDCs Maturation Following Mycobacterium bovis Infection
title_full cGAS/STING/TBK1/IRF3 Signaling Pathway Activates BMDCs Maturation Following Mycobacterium bovis Infection
title_fullStr cGAS/STING/TBK1/IRF3 Signaling Pathway Activates BMDCs Maturation Following Mycobacterium bovis Infection
title_full_unstemmed cGAS/STING/TBK1/IRF3 Signaling Pathway Activates BMDCs Maturation Following Mycobacterium bovis Infection
title_short cGAS/STING/TBK1/IRF3 Signaling Pathway Activates BMDCs Maturation Following Mycobacterium bovis Infection
title_sort cgas/sting/tbk1/irf3 signaling pathway activates bmdcs maturation following mycobacterium bovis infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6412216/
https://www.ncbi.nlm.nih.gov/pubmed/30791397
http://dx.doi.org/10.3390/ijms20040895
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