Activation of autophagy attenuates EtOH-LPS-induced hepatic steatosis and injury through MD2 associated TLR4 signaling

作者：Kong, Xiaoxia^*; Yang, Ying; Ren, Li; Shao, Tuo; Li, Fengyuan; Zhao, Cuiqing; Liu, Liming; Zhang, Hongyu; McClain, Craig J.; Feng, Wenke^*

来源：Scientific Reports, 2017, 7(1): 9292.

DOI：10.1038/s41598-017-09045-z

• INDUCED LIVER-INJURY
• TOLL-LIKE RECEPTORS
• OXIDATIVE STRESS
• FATTY LIVER
• DISEASE
• MICE
• HYPOXIA

Autophagy serves as a protective mechanism to degrade damaged organelles and proteins. Acute alcohol exposure is known to activate the hepatic autophagy response, whereas chronic alcohol exposure slows autophagosome formation along with an elevation of gut-derived endotoxin. In the current study, we examined whether lipopolysaccharide (LPS) administration decreased autophagic response in the liver of mice treated by short-term alcohol and whether activation of autophagy by rapamycin attenuates EtOH-LPS-induced liver steatosis and injury. We demonstrated that ten-day alcohol feeding primed the liver to LPS-induced lipid accumulation and liver injury with significantly increased hepatic steatosis and serum AST level as well as hepatic cellular NF-kappa B activation. LPS increased alcohol-mediated reactive oxygen species (ROS) formation while reducing autophagy activation. These deleterious effects were attenuated by rapamycin administration in mice. The protective effects of rapamycin are associated with decreased cellular MD2/TLR4 expression and interaction in Raw264.7 cells. Taken together, our results demonstrated that enhanced gut-derived LPS decreases the hepatic autophagosome numbers in response to alcohol exposure, and activation of autophagy by rapamycin protects from EtOH-LPS-induced liver injury, probably through reduced macrophage expression and interaction of TLR4/MD2 signaling complex.

• 出版日期2017-8-24
• 单位温州医科大学; 温州大学; 西安交通大学