» Articles » PMID: 36925453

Stress Granules Inhibit Endoplasmic Reticulum Stress-mediated Apoptosis During Hypoxia-induced Injury in Acute Liver Failure

Overview
Specialty Gastroenterology
Date 2023 Mar 17
PMID 36925453
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Stress granules (SGs) could be formed under different stimulation to inhibit cell injury.

Aim: To investigate whether SGs could protect hepatocytes from hypoxia-induced damage during acute liver failure (ALF) by reducing endoplasmic reticulum stress (ERS) mediated apoptosis.

Methods: The agonist of SGs, arsenite (Ars) was used to intervene hypoxia-induced hepatocyte injury cellular model and ALF mice models. Further, the siRNA of activating transcription factor 4 (ATF4) and SGs inhibitor anisomycin was then used to intervene in cell models.

Results: With the increase of hypoxia time from 4 h to 12 h, the levels of HIF-1α, ERS and apoptosis gradually increased, and the expression of SGs marker G3BP1 and TIA-1 was increased and then decreased. Compared with the hypoxia cell model group and ALF mice model, the levels of HIF-1α, apoptosis and ERS were increased in the Ars intervention group. After siRNA-ATF4 intervention, the level of SGs in cells increased, and the levels of HIF-1α, ERS and apoptosis decreased. Compared with the siRNA-ATF4 group, the levels of G3BP1 in the siRNA-ATF4+anisomycin group were decreased, and the levels of HIF-1α, ERS and apoptosis were increased. Moreover, compared with the ALF group, the degree of liver injury and liver function, the levels of HIF-1α, ERS and apoptosis in the Ars intervention group were decreased, the level of SGs was increased.

Conclusion: SGs could protect hepatocytes from hypoxia-induced damage during ALF by reducing ERS-mediated apoptosis.

Citing Articles

Biogenesis of stress granules and their role in the regulation of stress-induced male reproduction disorders.

Li J, Shen L, Wang K, Wu S, Wang Y, Pan Y Cell Commun Signal. 2025; 23(1):84.

PMID: 39948590 PMC: 11827146. DOI: 10.1186/s12964-025-02054-w.


Evaluation of G3BP1 in the prognosis of acute and acute-on-chronic liver failure after the treatment of artificial liver support system.

Li W, Wang L, Dong J, Wang Y World J Hepatol. 2024; 16(2):251-263.

PMID: 38495274 PMC: 10941744. DOI: 10.4254/wjh.v16.i2.251.


Protein aggregation and biomolecular condensation in hypoxic environments (Review).

Li C, Hao B, Yang H, Wang K, Fan L, Xiao W Int J Mol Med. 2024; 53(4).

PMID: 38362920 PMC: 10903932. DOI: 10.3892/ijmm.2024.5357.


The uncharted territory of host-pathogen interaction in tuberculosis.

Ghoshal A, Verma A, Bhaskar A, Dwivedi V Front Immunol. 2024; 15:1339467.

PMID: 38312835 PMC: 10834760. DOI: 10.3389/fimmu.2024.1339467.


Editor-in-Chief articles of choice and comments at the year-end of 2023.

Tarnawski A World J Gastroenterol. 2024; 30(1):1-8.

PMID: 38293322 PMC: 10823905. DOI: 10.3748/wjg.v30.i1.1.


References
1.
Torres S, Baulies A, Insausti-Urkia N, Alarcon-Vila C, Fucho R, Solsona-Vilarrasa E . Endoplasmic Reticulum Stress-Induced Upregulation of STARD1 Promotes Acetaminophen-Induced Acute Liver Failure. Gastroenterology. 2019; 157(2):552-568. DOI: 10.1053/j.gastro.2019.04.023. View

2.
Wang Y, Chen Q, Shi C, Jiao F, Gong Z . Mechanism of glycyrrhizin on ferroptosis during acute liver failure by inhibiting oxidative stress. Mol Med Rep. 2019; 20(5):4081-4090. PMC: 6797988. DOI: 10.3892/mmr.2019.10660. View

3.
Xin L, Fan W, Tingting D, Zuoming S, Qiang Z . 4-phenylbutyric acid attenuates endoplasmic reticulum stress-mediated apoptosis and protects the hepatocytes from intermittent hypoxia-induced injury. Sleep Breath. 2018; 23(2):711-717. DOI: 10.1007/s11325-018-1739-y. View

4.
McCormick C, Khaperskyy D . Translation inhibition and stress granules in the antiviral immune response. Nat Rev Immunol. 2017; 17(10):647-660. DOI: 10.1038/nri.2017.63. View

5.
Liu Y, Wang Y, Chen Q, Jiao F, Wang L, Gong Z . HDAC2 inhibitor CAY10683 reduces intestinal epithelial cell apoptosis by inhibiting mitochondrial apoptosis pathway in acute liver failure. Histol Histopathol. 2019; 34(10):1173-1184. DOI: 10.14670/HH-18-120. View