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The kinase p38α functions in dendritic cells to regulate Th2-cell differentiation and allergic inflammation

Dendritic cells (DCs) play a critical role in controlling T helper 2 (Th2) cell-dependent diseases, but the signaling mechanism that triggers this function is not fully understood. We showed that p38α activity in DCs was decreased upon HDM stimulation and dynamically regulated by both extrinsic sign...

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Autores principales: Han, Miaomiao, Ma, Jingyu, Ouyang, Suidong, Wang, Yanyan, Zheng, Tingting, Lu, Peishan, Zheng, Zihan, Zhao, Weiheng, Li, Hongjin, Wu, Yun, Zhang, Baohua, Hu, Ran, Otsu, Kinya, Liu, Xinguang, Wan, Ying, Li, Huabin, Huang, Gonghua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9243149/
https://www.ncbi.nlm.nih.gov/pubmed/35551270
http://dx.doi.org/10.1038/s41423-022-00873-2
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author Han, Miaomiao
Ma, Jingyu
Ouyang, Suidong
Wang, Yanyan
Zheng, Tingting
Lu, Peishan
Zheng, Zihan
Zhao, Weiheng
Li, Hongjin
Wu, Yun
Zhang, Baohua
Hu, Ran
Otsu, Kinya
Liu, Xinguang
Wan, Ying
Li, Huabin
Huang, Gonghua
author_facet Han, Miaomiao
Ma, Jingyu
Ouyang, Suidong
Wang, Yanyan
Zheng, Tingting
Lu, Peishan
Zheng, Zihan
Zhao, Weiheng
Li, Hongjin
Wu, Yun
Zhang, Baohua
Hu, Ran
Otsu, Kinya
Liu, Xinguang
Wan, Ying
Li, Huabin
Huang, Gonghua
author_sort Han, Miaomiao
collection PubMed
description Dendritic cells (DCs) play a critical role in controlling T helper 2 (Th2) cell-dependent diseases, but the signaling mechanism that triggers this function is not fully understood. We showed that p38α activity in DCs was decreased upon HDM stimulation and dynamically regulated by both extrinsic signals and Th2-instructive cytokines. p38α-specific deletion in cDC1s but not in cDC2s or macrophages promoted Th2 responses under HDM stimulation. Further study showed that p38α in cDC1s regulated Th2-cell differentiation by modulating the MK2−c-FOS−IL-12 axis. Importantly, crosstalk between p38α-dependent DCs and Th2 cells occurred during the sensitization phase, not the effector phase, and was conserved between mice and humans. Our results identify p38α signaling as a central pathway in DCs that integrates allergic and parasitic instructive signals with Th2-instructive cytokines from the microenvironment to regulate Th2-cell differentiation and function, and this finding may offer a novel strategy for the treatment of allergic diseases and parasitic infection.
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spelling pubmed-92431492022-07-01 The kinase p38α functions in dendritic cells to regulate Th2-cell differentiation and allergic inflammation Han, Miaomiao Ma, Jingyu Ouyang, Suidong Wang, Yanyan Zheng, Tingting Lu, Peishan Zheng, Zihan Zhao, Weiheng Li, Hongjin Wu, Yun Zhang, Baohua Hu, Ran Otsu, Kinya Liu, Xinguang Wan, Ying Li, Huabin Huang, Gonghua Cell Mol Immunol Article Dendritic cells (DCs) play a critical role in controlling T helper 2 (Th2) cell-dependent diseases, but the signaling mechanism that triggers this function is not fully understood. We showed that p38α activity in DCs was decreased upon HDM stimulation and dynamically regulated by both extrinsic signals and Th2-instructive cytokines. p38α-specific deletion in cDC1s but not in cDC2s or macrophages promoted Th2 responses under HDM stimulation. Further study showed that p38α in cDC1s regulated Th2-cell differentiation by modulating the MK2−c-FOS−IL-12 axis. Importantly, crosstalk between p38α-dependent DCs and Th2 cells occurred during the sensitization phase, not the effector phase, and was conserved between mice and humans. Our results identify p38α signaling as a central pathway in DCs that integrates allergic and parasitic instructive signals with Th2-instructive cytokines from the microenvironment to regulate Th2-cell differentiation and function, and this finding may offer a novel strategy for the treatment of allergic diseases and parasitic infection. Nature Publishing Group UK 2022-05-12 2022-07 /pmc/articles/PMC9243149/ /pubmed/35551270 http://dx.doi.org/10.1038/s41423-022-00873-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Han, Miaomiao
Ma, Jingyu
Ouyang, Suidong
Wang, Yanyan
Zheng, Tingting
Lu, Peishan
Zheng, Zihan
Zhao, Weiheng
Li, Hongjin
Wu, Yun
Zhang, Baohua
Hu, Ran
Otsu, Kinya
Liu, Xinguang
Wan, Ying
Li, Huabin
Huang, Gonghua
The kinase p38α functions in dendritic cells to regulate Th2-cell differentiation and allergic inflammation
title The kinase p38α functions in dendritic cells to regulate Th2-cell differentiation and allergic inflammation
title_full The kinase p38α functions in dendritic cells to regulate Th2-cell differentiation and allergic inflammation
title_fullStr The kinase p38α functions in dendritic cells to regulate Th2-cell differentiation and allergic inflammation
title_full_unstemmed The kinase p38α functions in dendritic cells to regulate Th2-cell differentiation and allergic inflammation
title_short The kinase p38α functions in dendritic cells to regulate Th2-cell differentiation and allergic inflammation
title_sort kinase p38α functions in dendritic cells to regulate th2-cell differentiation and allergic inflammation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9243149/
https://www.ncbi.nlm.nih.gov/pubmed/35551270
http://dx.doi.org/10.1038/s41423-022-00873-2
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