The study of GSDMB in pathogenesis of psoriasis vulgaris

PLoS One. 2023 Jan 6;18(1):e0279908. doi: 10.1371/journal.pone.0279908. eCollection 2023.

Abstract

Background: Gasdermin (GSDM) B is a member of the GSDM family, which is a protein that may be involved in the cell pyroptosis process and is associated with inflammatory diseases.

Objective: To explore the correlation between GSDMB and psoriasis vulgaris.

Methods: Skin lesions from 33 patients with psoriasis vulgaris and 69 normal controls were collected. ELISA and Western blot were adopted to detect proteins. The HaCaT cell line was transfected with 3 sets of interfering sequence siRNA, and the mRNA and protein levels before and after the transfection were measured by qPCR and Western blot respectively, so as to establish a cell model with low GSDMB gene expression; the MTT method was used to detect cells viability, flow cytometry to detect cell apoptosis.

Results: The level of GSDMB protein in the skin lesions of patients with psoriasis vulgaris was lower than that in normal skin tissues (P < 0.05). The mRNA and protein expression levels of the target gene in the siRNA-GSDMB-3 group were lower than those in the control group (P < 0.05). The proliferation of HaCaT cells was decreased by MTT method and flow cytometry, and the apoptosis rate was increased (P < 0.05).

Conclusion: The expression level of GSDMB in psoriasis vulgaris lesion tissue is lower than that of normal skin tissue. The down-regulation of GSDMB expression can inhibit cell proliferation and promote cell apoptosis. GSDMB may play a role in the pathogenesis of psoriasis by affecting the differentiation of keratinocytes and the function of T cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Proliferation
  • Humans
  • Keratinocytes / metabolism
  • Pore Forming Cytotoxic Proteins / metabolism
  • Psoriasis* / pathology
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / metabolism
  • Skin / metabolism

Substances

  • RNA, Small Interfering
  • RNA, Messenger
  • GSDMB protein, human
  • Pore Forming Cytotoxic Proteins

Grants and funding

Funding for this work: Science and Technology Research Project of Education Department of Jiangxi Province. Grant number: GJJ170887 The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.