Acid-sensing ion channel 1a promotes alcohol-associated liver disease in mice via regulating endoplasmic reticulum autophagy

Acta Pharmacol Sin. 2025 Apr;46(4):989-1001. doi: 10.1038/s41401-024-01423-4. Epub 2024 Nov 26.

Abstract

Alcohol-associated liver disease (ALD) is a hepatocyte dysfunction disease caused by chronic or excessive alcohol consumption, which can lead to extensive hepatocyte necrosis and even liver failure. Currently, the pathogenesis of ALD and the anti-ALD mechanisms have not been fully elucidated yet. In this study, we investigated the effects of endoplasmic reticulum autophagy (ER-phagy) in ALD and the role of acid-sensing ion channel 1a (ASIC1a) in ER stress-mediated ER-phagy. A mouse model of ALD was established using the Gao-Binge method and the AML12 cell line treated with alcohol was used as an in vitro model. We showed that ASIC1a expression was significantly increased and ER-phagy was activated in both the in vivo and in vitro models. In alcohol-treated AML12 cells, we showed that blockade of ASIC1a with PcTx-1 or knockdown of ASIC1a reduced alcohol-induced intracellular Ca2+ accumulation and ER stress. In addition, inhibition of ER stress with 4-PBA reduced the level of ER-phagy. Furthermore, knockdown of the ER-phagy receptor family with sequence similarity 134 member B (FAM134B) alleviated alcohol-triggered hepatocyte injury and apoptosis. In conclusion, this study demonstrates that alcohol activates ER stress-induced ER-phagy and liver injury by increasing ASIC1a expression and ASIC1a-mediated Ca2+ influx, providing a novel strategy for the treatment of ALD.

Keywords: ASIC1a; Ca2+ influx; ER stress; ER-phagy; alcohol-associated liver disease; apoptosis.

MeSH terms

  • Acid Sensing Ion Channels* / genetics
  • Acid Sensing Ion Channels* / metabolism
  • Animals
  • Apoptosis / drug effects
  • Autophagy* / drug effects
  • Calcium / metabolism
  • Cell Line
  • Endoplasmic Reticulum Stress* / drug effects
  • Endoplasmic Reticulum* / drug effects
  • Endoplasmic Reticulum* / metabolism
  • Ethanol*
  • Hepatocytes / drug effects
  • Hepatocytes / metabolism
  • Liver Diseases, Alcoholic* / metabolism
  • Liver Diseases, Alcoholic* / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL*
  • Peptides
  • Spider Venoms / pharmacology

Substances

  • Acid Sensing Ion Channels
  • Ethanol
  • ASIC1 protein, mouse
  • Calcium
  • Spider Venoms
  • PcTX1 protein, Psalmopoeus cambridgei
  • Peptides