Down-regulation of long noncoding RNA LINC00472 alleviates sepsis-induced acute hepatic injury by regulating miR-373-3p/TRIM8 axis

Exp Mol Pathol. 2020 Dec:117:104562. doi: 10.1016/j.yexmp.2020.104562. Epub 2020 Oct 28.

Abstract

Background: The long noncoding RNAs (lncRNAs) have been confirmed to be involved in sepsis-induced organ injury. Here, we first investigated the functional role and the underlying mechanism of lncRNA LINC00472 in sepsis-induced acute hepatic injury (AHI).

Methods: Human liver THLE-3 cells were treated with lipopolysaccharide (LPS) to mimic sepsis-induced AHI in vitro; intraperitoneal injection of LPS in rats were used as an in vivo model of AHI induced by sepsis. The expressions of LINC00472, miR-373-3p, and TRIM8 mRNA were detected by qRT-PCR. The effects of LINC00472 and miR-373-3p on the viability of THLE-3 cells were assessed by CCK-8 assay. Dual-luciferase reporter and RNA immunoprecipitation (RIP) assays were performed to determine the binding relationship between LINC00472 and miR-373-3p as well as between miR-373-3p and TRIM8. The expressions of apoptosis-related proteins and TRIM8 were detected by Western blot; the levels of ALT, AST, TNF-α, IL-6, and IL-10 in the serum of rats were measured using ELSA assay.

Results: LINC00472 and TRIM8 were significantly upregulated in liver tissues and THLE-3 cells in sepsis-induced AHI models, while miR-373-3p was downregulated. Silencing of LINC00472 promoted cell viability and suppressed cell apoptosis in LPS-treated THLE-3 cells, whereas upregulation of LINC00472 had the opposite effect. Moreover, LINC00472 served as a sponge for miR-373-3p and negatively regulated its expression. miR-373-3p mimics could promote THLE-3 cell viability and suppress cell apoptosis. Additionally, TRIM8 was a direct target of miR-373-3p, which was downregulated in LINC00472-silenced cells and upregulated by the miR-373-3p inhibitor. Further, the co-transfection of miR-373-3p inhibitor reversed the effects of LINC00472 knockdown on cell viability and apoptosis. Downregulation of LINC00472 in rats restored the levels of ALT, AST, IL-6, IL-10, and TNF-α.

Conclusion: Downregulation of LINC00472 ameliorates sepsis-induced AHI by regulating the miR-373-3p/TRIM8 axis.

Keywords: Acute hepatic injury; LINC00472; Sepsis; TRIM8; miR-373-3p.

MeSH terms

  • Animals
  • Apoptosis / genetics
  • Carrier Proteins / genetics*
  • Cell Proliferation / genetics
  • Cell Survival / genetics
  • Disease Models, Animal
  • Gene Expression Regulation / genetics
  • Humans
  • Lipopolysaccharides / toxicity
  • Liver / injuries
  • Liver / metabolism
  • Liver / pathology
  • Liver Diseases / etiology
  • Liver Diseases / genetics*
  • Liver Diseases / pathology
  • Male
  • MicroRNAs / genetics*
  • Nerve Tissue Proteins / genetics*
  • RNA, Long Noncoding / genetics*
  • Rats
  • Sepsis / chemically induced
  • Sepsis / complications
  • Sepsis / genetics*
  • Sepsis / pathology

Substances

  • Carrier Proteins
  • LINC00472 RNA, human
  • Lipopolysaccharides
  • MIRN373 microRNA, human
  • MicroRNAs
  • Nerve Tissue Proteins
  • RNA, Long Noncoding
  • TRIM8 protein, human