MED1 mediator subunit is a key regulator of hepatic autophagy and lipid metabolism.

ABSTRACT

Hepatic macroautophagy/autophagy and fatty acid metabolism are transcriptionally regulated by nuclear receptors (NRs); however, it is not known whether their transcriptional co-activators are involved in autophagy. We thus examined MED1 (mediator complex subunit 1), a key component of the Mediator Complex that directly interacts with NRs, on these processes. We found that MED1 knockdown (KD) in cultured hepatic cells decreased autophagy and mitochondrial activity that was accompanied by decreased transcription of genes involved in these processes. Lipophagy and fatty acid ß-oxidation also were impaired. These effects also occurred after thyroid hormone stimulation, nutrient-replete or -deplete conditions, and in liver-specific Med1 KD (Med1 LKD) mice under fed and fasting conditions. Together, these findings showed that Med1 played a key role in hepatic autophagy, mitochondria function, and lipid metabolism under these conditions. Additionally, we identified downregulated hepatic genes in Med1 LKD mice, and subjected them to ChIP Enrichment Analysis. Our findings showed that the transcriptional activity of several NRs and transcription factors (TFs), including PPARA and FOXO1, likely were affected by Med1 LKD. Finally, Med1 expression and autophagy also were decreased in two mouse models of nonalcoholic fatty liver disease (NAFLD) suggesting that decreased Med1 may contribute to hepatosteatosis. In summary, MED1 plays an essential role in regulating hepatic autophagy and lipid oxidation during different hormonal and nutrient conditions. Thus, MED1 may serve as an integrator of multiple transcriptional pathways involved in these metabolic processes.Abbreviations BAF bafilomycin A1; db/db mice; Leprdb/db mice; ECAR extracellular acidification rate; KD knockdown; MED1 mediator complex subunit 1; NAFLD nonalcoholic fatty liver disease; OCR oxygen consumption rate; PPARA/PPARα peroxisomal proliferator activated receptor alpha; TF transcription factor; TFEB transcription factor EB; tf-LC3 tandem fluorescence RFP-GFP-LC3; TG triglyceride; TH Thyroid hormone; TR thyroid hormone receptors; V-ATPase vacuolar-type H+-ATPase; WDF Western diet with 15% fructose in drinking water.