Cross-disease characterization of fibroblast heterogeneities and their pathogenic roles in skin inflammation
Copyright © 2023 Elsevier Inc. All rights reserved.
Publié dans: | Clinical immunology (Orlando, Fla.). - 1999. - 255(2023) vom: 15. Okt., Seite 109742 |
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Auteur principal: | |
Autres auteurs: | , , , , , , , , , , , , |
Format: | Article en ligne |
Langue: | English |
Publié: |
2023
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Accès à la collection: | Clinical immunology (Orlando, Fla.) |
Sujets: | Journal Article COL6A5 Cross-disease Fibroblast Heterogeneity Psoriasis |
Résumé: | Copyright © 2023 Elsevier Inc. All rights reserved. Fibroblasts are critical pro-inflammatory regulators in chronic inflammatory and fibrotic skin diseases. However, fibroblast heterogeneity and the absence of a unified cross-disease taxonomy have hindered our understanding of the shared/distinct pathways in non-communicable skin inflammation. By integrating 10× single-cell data from 75 skin samples, we constructed a single-cell atlas across inflammatory and fibrotic skin diseases and identified 9 distinct subsets of skin fibroblasts. We found a shared subset of CCL19+ fibroblasts across these diseases, potentially attracting and educating immune cells. Moreover, COL6A5+ fibroblasts were a distinct subset implicated in the initiation and relapse of psoriasis, which tended to differentiate into CXCL1+ fibroblasts, inducing neutrophil chemotaxis and infiltration; while CXCL1+ fibroblasts exhibited a more heterogeneous response to certain inflammatory conditions. Differentiation trajectory and regulatory factors of these fibroblast subsets were also revealed. Therefore, our study presents a comprehensive atlas of skin fibroblasts and highlights pathogenic fibroblast subsets in skin disorders |
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Description: | Date Revised 28.09.2023 published: Print-Electronic Citation Status Publisher |
ISSN: | 1521-7035 |
DOI: | 10.1016/j.clim.2023.109742 |