Induction of IL-32 in the immune response of keratinocytes to Mycobacterium marinum infection.

Exp Dermatol

Shandong Provincial Hospital for Skin Diseases & Shandong Provincial Institute of Dermatology and Venereology, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan, China.

Published: September 2023

AI Article Synopsis

  • * Researchers conducted single-cell and bulk RNA sequencing on skin samples from patients with Mycobacterium marinum infection and found that certain genes, including IL-32, were significantly upregulated in infected keratinocytes.
  • * The study indicates that IL-32 may play a key role in how keratinocytes respond to M. marinum, suggesting potential new targets for treating chronic skin mycobacterial infections.

Article Abstract

Keratinocytes are the predominant cell type in the skin epidermis, and they not only protect the skin from the influence of external physical factors but also function as an immune barrier against microbial invasion. However, little is known regarding the immune defence mechanisms of keratinocytes against mycobacteria. Here, we performed single-cell RNA sequencing (scRNA-seq) on skin biopsy samples from patients with Mycobacterium marinum infection and bulk RNA sequencing (bRNA-seq) on M. marinum-infected keratinocytes in vitro. The combined analysis of scRNA-seq and bRNA-seq data revealed that several genes were upregulated in M. marinum-infected keratinocytes. Further in vitro validation of these genes by quantitative polymerase chain reaction and western blotting assay confirmed the induction of IL-32 in the immune response of keratinocytes to M. marinum infection. Immunohistochemistry also showed the high expression of IL-32 in patients' lesions. These findings suggest that IL-32 induction is a possible mechanism through which keratinocytes defend against M. marinum infection; this could provide new targets for the immunotherapy of chronic cutaneous mycobacterial infections.

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http://dx.doi.org/10.1111/exd.14848DOI Listing

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