OAS3 Deubiquitination Due to E3 Ligase TRIM21 Downregulation Promotes Epithelial Cell Apoptosis and Drives Sepsis-induced Acute Lung Injury

Int J Biol Sci. 2024 Oct 14;20(14):5594-5607. doi: 10.7150/ijbs.96089. eCollection 2024.

Abstract

Patients with sepsis-induced acute lung injury (SALI) show a high mortality rate, and there is no effective treatment in the clinic for SALI but only symptomatic treatment as an option. Therefore, searching for effective targets is critical for the management of SALI. Ubiquitination is an essential post-translational protein modification involved in most pathophysiological processes. However, the relationship between ubiquitination and SALI remains largely unclear. In this study, we examined the ubiquitination modification changes in SALI, identified oligoadenylate synthetase 3 (OAS3) as a key candidate accounting for SALI from integrative multi-omics analysis and confirmed its role in promoting SALI and cell apoptosis in an animal model of cecal ligation and puncture-treated mice and a cellular model of LPS-treated MLE12 cells. Mechanistically, downregulation of E3 ligase TRIM21 mediates the reduction of OAS3 K48-linked polyubiquitination at the K1079 site in lung epithelial cells of a septic model, which leads to the increase of OAS3 protein level in a proteasomal-dependent manner. The upregulated OAS3 promotes epithelial cell apoptosis through its downstream effector molecule, RNase L. In summary, these findings unveil a previously unappreciated role of OAS3 ubiquitination in SALI and offer a promising perspective for further understanding the development of sepsis and potential therapeutic target for the treatment of SALI.

Keywords: Acute lung injury; Apoptosis; OAS3; Sepsis; TRIM21; Ubiquitination.

MeSH terms

  • 2',5'-Oligoadenylate Synthetase* / genetics
  • 2',5'-Oligoadenylate Synthetase* / metabolism
  • Acute Lung Injury* / etiology
  • Acute Lung Injury* / metabolism
  • Animals
  • Apoptosis*
  • Cell Line
  • Down-Regulation
  • Epithelial Cells* / metabolism
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Ribonucleoproteins / metabolism
  • Sepsis* / complications
  • Sepsis* / metabolism
  • Ubiquitin-Protein Ligases / genetics
  • Ubiquitin-Protein Ligases / metabolism
  • Ubiquitination*

Substances

  • 2',5'-Oligoadenylate Synthetase
  • SS-A antigen
  • Ubiquitin-Protein Ligases
  • Ribonucleoproteins