Open Access

IRF2 contributes to myocardial infarction via regulation of GSDMD induced pyroptosis

  • Authors:
    • Yongxing Li
    • Yan Wang
    • Hua Guo
    • Qinghua Wu
    • Yamin Hu
  • View Affiliations

  • Published online on: December 6, 2021     https://doi.org/10.3892/mmr.2021.12556
  • Article Number: 40
  • Copyright: © Li et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Abstract

Interferon regulatory factor (IRF) 2 is a transcription factor belonging to the IRF family, which is essential for gasdermin D (GSDMD)‑induced pyroptosis. Decreasing myocardial cell pyroptosis confers protection against heart damage and cardiac dysfunction caused by myocardial infarction (MI). The aim of the present study was to investigate the involvement of IRF2 in MI and the underlying mechanism of IRF2 in pyroptosis. To mimic MI, ligation of the left anterior descending coronary artery was performed to establish an in vivo mouse model and rat cardiomyocytes H9c2 cells were cultured under hypoxic conditions to establish an in vitro model. Transthoracic echocardiography was used to assess cardiac function. Hematoxylin and eosin staining was used to observe histopathological changes in the myocardial tissue. Immunohistochemistry and western blotting were performed to detect IRF2 expression levels. TUNEL staining and flow cytometry were used to detect apoptosis in myocardial tissue and cells. Chromatin immunoprecipitation and dual luciferase reporter assay were used to verify the effect of IRF2 on GSDMD transcription. IRF2 was upregulated in MI mice. MI induced pyroptosis, as evidenced by increased GSDMD, N‑terminal GSDMD (GSDMD‑N), and cleaved (c‑) caspase‑1 levels. MI increased IL‑1β and IL‑18 levels. These alterations were alleviated by IRF2 silencing. Furthermore, in hypoxia‑treated H9c2 cells, IRF2 silencing significantly decreased the elevated levels of IL‑1β and IL‑18 and pyroptosis‑associated proteins, including GSDMD, GSDMD‑N and c‑caspase1. Moreover, in hypoxia‑treated H9c2 cells, IRF2 directly bound to the GSDMD promoter to drive GSDMD transcription and promote pyroptosis and IRF2 expression may be regulated via the hypoxia inducible factor 1 signaling pathway. In conclusion, the present results demonstrated that IRF2 is a key regulator of MI by mediating pyroptosis, which triggers GSDMD activation.
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February-2022
Volume 25 Issue 2

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Copy and paste a formatted citation
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Spandidos Publications style
Li Y, Wang Y, Guo H, Wu Q and Hu Y: IRF2 contributes to myocardial infarction via regulation of GSDMD induced pyroptosis. Mol Med Rep 25: 40, 2022
APA
Li, Y., Wang, Y., Guo, H., Wu, Q., & Hu, Y. (2022). IRF2 contributes to myocardial infarction via regulation of GSDMD induced pyroptosis. Molecular Medicine Reports, 25, 40. https://doi.org/10.3892/mmr.2021.12556
MLA
Li, Y., Wang, Y., Guo, H., Wu, Q., Hu, Y."IRF2 contributes to myocardial infarction via regulation of GSDMD induced pyroptosis". Molecular Medicine Reports 25.2 (2022): 40.
Chicago
Li, Y., Wang, Y., Guo, H., Wu, Q., Hu, Y."IRF2 contributes to myocardial infarction via regulation of GSDMD induced pyroptosis". Molecular Medicine Reports 25, no. 2 (2022): 40. https://doi.org/10.3892/mmr.2021.12556