Unfolded protein response factor ATF6 augments T helper cell responses and promotes mixed granulocytic airway inflammation
Year: 2023
Type: article
Abstract: The unfolded protein response (UPR) is associated with the risk of asthma, including treatment- refractory severe asthma. Several recent studies demonstrated a pathogenic role of activating transcription factor 6α (ATF6α or ATF6), one of the essential arms of UPR, in airway structural cells. However, its role in T helper (TH) cells has not been well examined. In this study, we found that ATF6 was selectively induced by STAT6 and STAT3 in TH2 and TH17 cells, respectively. ATF6 upregulated UPR genes and promoted the differentiation and cytokine secretion of TH2 and TH17 cells. T cell-specific Atf6 -deficiency impaired TH2 and TH17 responses in vitro and in vivo and attenuated mixed granulocytic experimental asthma. ATF6 inhibitor Ceapin A7 suppressed ATF6 downstream gene expression and TH cell cytokine expression in both murine and human memory CD4 + T cells. At the chronic stage of asthma, administration of Ceapin A7 lessened TH2 and TH17 responses in vivo , leading to alleviation of both airway neutrophilia and eosinophilia. Thus, our results demonstrate a critical role of ATF6 in TH2 and TH17 cell-driven mixed granulocytic airway disease, suggesting a novel option to combat steroid-resistant mixed and even T2-low endotypes of asthma by targeting ATF6.
Source: Mucosal Immunology
Language: English
Subfield: Physiology
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $3,800
Funders: National Institutes of Health, Comprehensive Cancer Center, University of Michigan, National Heart, Lung, and Blood Institute, National Cancer Institute, National Institute of General Medical Sciences, National Institute of Allergy and Infectious Diseases, National Institute of Diabetes and Digestive and Kidney Diseases
Awards: G10775630, G1849608474, The Cytokine Suppressor CIS in Giant Cell Pneumonitis, G7047137344, Leptin Promotes Allergic Asthma through Unfolded Protein Responses, G9000113981, G9000115479, G9000150615, G9000308376, University of New Mexico Center for Metals in Biology and Medicine, University of New Mexico Cancer Center Support Grant, Autophagy, Inflammation and Metabolism (AIM) in Disease Center - Phase 2., Transcriptional Control of High-thermogenic Adipocyte Development
OpenAlex ID: W4377138692
