Exosomal miR-181a-2-3p derived from citreoviridin-treated hepatocytes activates hepatic stellate cells trough inducing mitochondrial calcium overload

Chem Biol Interact. 2022 May 1:358:109899. doi: 10.1016/j.cbi.2022.109899. Epub 2022 Mar 16.

Abstract

Increasing evidences indicate the vital role of exosomes-mediated intercellular communication in the pathogenesis of liver fibrosis. However, the underlying mechanisms are still not clearly defined. In this study, we found that citreoviridin (CIT), a mycotoxin and ectopic ATP synthase (e-ATPS) inhibitor, induced liver fibrosis in mice. The exosomes derived from CIT-treated L-02 hepatocytes activated hepatic stellate cells (HSC) LX-2. With exosomal small RNA sequencing, we found 156 differentially expressed miRNAs in the exosomes from CIT-treated L-02 cells, and the predicted target genes of exosomal miRNAs were enriched in calcium signaling pathway. The exosomes from CIT-treated L-02 cells induced mitochondrial calcium accumulation in LX-2 cells. And pharmacological inhibition of mitochondrial calcium uptake relieved exosomes-activated fibrogenic response in LX-2 cells. The miR-181a-2-3p that was predicted to target-regulate mitochondrial calcium uptake 1 (MICU1) was significantly increased in the exosomes from CIT-treated L-02 cells. Exosomes-induced reduction of MICU1, mitochondrial calcium overload and activation of LX-2 cells were reversed by AntagomiR-181a-2-3p. In this study, we pointed out that exosomal miR-181a-2-3p from CIT-treated hepatocytes induced mitochondrial calcium accumulation and activated HSC subsequently through inhibiting the expression of MICU1, shedding new light on the mechanism underlying liver fibrosis and CIT hepatotoxicity.

Keywords: Citreoviridin; Ectopic ATP synthase; Exosomal miRNA; Liver fibrosis; Mitochondrial calcium.

MeSH terms

  • Animals
  • Aurovertins / pharmacology
  • Calcium* / metabolism
  • Calcium-Binding Proteins / metabolism
  • Exosomes / metabolism
  • Hepatic Stellate Cells* / drug effects
  • Hepatic Stellate Cells* / metabolism
  • Hepatocytes / drug effects
  • Hepatocytes / metabolism
  • Liver Cirrhosis* / chemically induced
  • Liver Cirrhosis* / metabolism
  • Mice
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • Mitochondria, Liver* / drug effects
  • Mitochondria, Liver* / metabolism
  • Mitochondrial Membrane Transport Proteins / metabolism
  • Signal Transduction / genetics

Substances

  • Aurovertins
  • Calcium-Binding Proteins
  • MICU1 protein, mouse
  • MicroRNAs
  • Mitochondrial Membrane Transport Proteins
  • mirn181 microRNA, mouse
  • citreoviridin
  • Calcium