PLoS ONE · 2014 · 177 citations · 22 references
Life SciencesBiochemistryPharmacologyAutophagyInflammationLipid BiochemistryAutophagy DysregulationAutophagy ModulationAutophagy PharmacologyAutophagy RegulationAutophagy Signaling PathwaysLipid MetabolismAutophagic ClearanceAutophagic Flux ModulationAutophagic Flux RegulationAutophagy In Liver MetabolismLipid Droplet FormationLipid Metabolism EffectsLipid Metabolism PathwaysLysosomal Acidification
Epigallocatechin gallate (EGCG) is a major polyphenol in green tea that has been shown to have anti-inflammatory, anti-cancer, anti-steatotic effects on the liver. Autophagy also mediates similar effects; however, it is not currently known whether EGCG can regulate hepatic autophagy. Here, we show that EGCG increases hepatic autophagy by promoting the formation of autophagosomes, increasing lysosomal acidification, and stimulating autophagic flux in hepatic cells and in vivo. EGCG also increases phosphorylation of AMPK, one of the major regulators of autophagy. Importantly, siRNA knockdown of AMPK abrogated autophagy induced by EGCG. Interestingly, we observed lipid droplet within autophagosomes and autolysosomes and increased lipid clearance by EGCG, suggesting it promotes lipid metabolism by increasing autophagy. In mice fed with high-fat/western style diet (HFW; 60% energy as fat, reduced levels of calcium, vitamin D3, choline, folate, and fiber), EGCG treatment reduces hepatosteatosis and concomitantly increases autophagy. In summary, we have used genetic and pharmacological approaches to demonstrate EGCG induction of hepatic autophagy, and this may contribute to its beneficial effects in reducing hepatosteatosis and potentially some other pathological liver conditions.
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