School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032 Anhui, China.
Biopharmaceutical Research Institute, Anhui Medical University, Hefei, China.
Oxid Med Cell Longev. 2020 Jul 7;2020:9034864. doi: 10.1155/2020/9034864. eCollection 2020.
Consumption of alcohol in immoderate quantity induces endoplasmic reticulum (ER) stress response (alcohol-induced ER stress). Mesencephalic astrocyte-derived neurotrophic factor (MANF), an ER stress-inducible protein, works as an evolutionarily conserved regulator of systemic and liver metabolic homeostasis. In this study, the effects of MANF on alcohol-induced liver injury were explored by using hepatocyte-specific MANF-knockout mice (MANF ) in a chronic-plus-binge alcohol feeding model. We found that alcohol feeding upregulated MANF expression and MANF mice exhibited more severe liver injury with extra activated ER stress after alcohol feeding. In addition, we found that MANF deficiency activated iNOS and p65 and increased the production of NO and anti-inflammatory cytokines, which was further enhanced after alcohol treatment. Meanwhile, MANF deletion upregulated the levels of CYP2E1, 4-HNE, and MDA and downregulated the levels of GSH and SOD. These results indicate that MANF has potential protection on alcohol-induced liver injury, and the underlying mechanisms may be associated with meliorating the overactivated ER stress triggered by inflammation and oxidative stress via inhibiting and reducing NO/NF-B and CYP2E1/ROS, respectively. Therefore, MANF might be a negative regulator in alcohol-induced ER stress and participate in the crosstalk between the NF-B pathway and oxidative stress in the liver. . This study identifies a specific role of MANF in alcohol-induced liver injury, which may provide a new approach for the treatment of ALI.
过量饮酒会诱导内质网(ER)应激反应(酒精诱导的 ER 应激)。中脑星形胶质细胞衍生的神经营养因子(MANF)是一种 ER 应激诱导蛋白,作为一种进化上保守的系统和肝脏代谢稳态调节剂。在这项研究中,通过使用肝细胞特异性 MANF 敲除小鼠(MANF -/- )在慢性加 binge 酒精喂养模型中,研究了 MANF 对酒精性肝损伤的影响。我们发现,酒精喂养上调了 MANF 的表达,而 MANF -/- 小鼠在酒精喂养后表现出更严重的肝损伤,内质网应激过度激活。此外,我们发现 MANF 缺乏激活了 iNOS 和 p65,并增加了 NO 和抗炎细胞因子的产生,而在酒精处理后进一步增强。同时,MANF 缺失上调了 CYP2E1、4-HNE 和 MDA 的水平,降低了 GSH 和 SOD 的水平。这些结果表明,MANF 对酒精性肝损伤具有潜在的保护作用,其潜在机制可能与通过抑制和减少 NO/NF-B 和 CYP2E1/ROS 分别改善由炎症和氧化应激引发的过度激活的 ER 应激有关。因此,MANF 可能是酒精诱导的 ER 应激中的负调控因子,并参与 NF-B 途径和肝脏氧化应激之间的串扰。这项研究确定了 MANF 在酒精性肝损伤中的特定作用,这可能为 ALI 的治疗提供新的方法。