IL-1β-induced epithelial cell and fibroblast transdifferentiation promotes neutrophil recruitment in chronic rhinosinusitis with nasal polyps

Neutrophilic inflammation contributes to multiple chronic inflammatory airway diseases, including asthma and chronic rhinosinusitis with nasal polyps (CRSwNP), and is associated with an unfavorable prognosis. Here, using single-cell RNA sequencing (scRNA-seq) to profile human nasal mucosa obtained from the inferior turbinates, middle turbinates, and nasal polyps of CRSwNP patients, we identify two IL-1 signaling-induced cell subsets-LY6D<sup>+</sup> club cells and IDO1<sup>+</sup> fibroblasts-that promote neutrophil recruitment by respectively releasing S100A8/A9 and CXCL1/2/3/5/6/8 into inflammatory regions. IL-1β, a pro-inflammatory cytokine involved in IL-1 signaling, induces the transdifferentiation of LY6D<sup>+</sup> club cells and IDO1<sup>+</sup> fibroblasts from primary epithelial cells and fibroblasts, respectively. In an LPS-induced neutrophilic CRSwNP mouse model, blocking IL-1β activity with a receptor antagonist significantly reduces the numbers of LY6D<sup>+</sup> club cells and IDO1<sup>+</sup> fibroblasts and mitigates nasal inflammation. This study implicates the function of two cell subsets in neutrophil recruitment and demonstrates an IL-1-based intervention for mitigating neutrophilic inflammation in CRSwNP.

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Publication Details

Journal
Nature Communications
Published
2024-10-22
DOI
https://doi.org/10.1038/s41467-024-53307-0
Citations
33
Primary Topic
Sinusitis and nasal conditions
Type
article
Field-Weighted Citation Impact
19.13

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article

IL-1β-induced epithelial cell and fibroblast transdifferentiation promotes neutrophil recruitment in chronic rhinosinusitis with nasal polyps

Pin Wang, Changhua Wu, Xuezhong Li, Xin Feng et al.
33 citations
Nature Communications
Sinusitis and nasal conditions
19.13
article

IL-1β-induced epithelial cell and fibroblast transdifferentiation promotes neutrophil recruitment in chronic rhinosinusitis with nasal polyps

Pin Wang, Changhua Wu, Xuezhong Li, Xin Feng, Fangying Liu, Xinyu Xie, Shu Guo, Min Jin, Larry Borish, Weiyuan Liu, Xiaojun Zhang, Heng Liu, Wei Zhao, Yue Wang, Changqing Li, Ping Ye, Xinyi Ma, Ye Yuan, Lijie Qi, Chen Duan
article en
33 citations

Abstract

Neutrophilic inflammation contributes to multiple chronic inflammatory airway diseases, including asthma and chronic rhinosinusitis with nasal polyps (CRSwNP), and is associated with an unfavorable prognosis. Here, using single-cell RNA sequencing (scRNA-seq) to profile human nasal mucosa obtained from the inferior turbinates, middle turbinates, and nasal polyps of CRSwNP patients, we identify two IL-1 signaling-induced cell subsets-LY6D<sup>+</sup> club cells and IDO1<sup>+</sup> fibroblasts-that promote neutrophil recruitment by respectively releasing S100A8/A9 and CXCL1/2/3/5/6/8 into inflammatory regions. IL-1β, a pro-inflammatory cytokine involved in IL-1 signaling, induces the transdifferentiation of LY6D<sup>+</sup> club cells and IDO1<sup>+</sup> fibroblasts from primary epithelial cells and fibroblasts, respectively. In an LPS-induced neutrophilic CRSwNP mouse model, blocking IL-1β activity with a receptor antagonist significantly reduces the numbers of LY6D<sup>+</sup> club cells and IDO1<sup>+</sup> fibroblasts and mitigates nasal inflammation. This study implicates the function of two cell subsets in neutrophil recruitment and demonstrates an IL-1-based intervention for mitigating neutrophilic inflammation in CRSwNP.

Nature CommunicationsVol. 15(1)
Shandong University (CN), University of Virginia Health System (US), Qilu Hospital of Shandong University (CN)
Taishan Scholar Foundation of Shandong Province, National Natural Science Foundation of China, Natural Science Foundation of Shandong Province
Zero hunger
Openalex Percentile: Top 0%
Sinusitis and nasal conditions
19.13
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