A novel role of astrocyte elevated gene‐1 (AEG‐1) in regulating nonalcoholic steatohepatitis (NASH). Issue 2 (30th June 2017)

• Record Type: Journal Article
• Authors: Srivastava, Jyoti; Robertson, Chadia L.; Ebeid, Kareem; Dozmorov, Mikhail; Rajasekaran, Devaraja; Mendoza, Rachel; Siddiq, Ayesha; Akiel, Maaged A.; Jariwala, Nidhi; Shen, Xue‐Ning; Windle, Jolene J.; Subler, Mark A.; Mukhopadhyay, Nitai D.; Giashuddin, Shah; Ghosh, Shobha; Lai, Zhao; Chen, Yidong; Fisher, Paul B.; Salem, Aliasger K.; Sanyal, Arun J.; Sarkar, Devanand
• Is Part Of: Hepatology. Volume 66:Issue 2(2017)
• Page Start: 466
• Page End: 480
• Publication Date: 2017-06-30
• Subjects: Heart -- Diseases -- Nursing -- Periodicals; Lungs -- Diseases -- Nursing -- Periodicals; Intensive care nursing -- Periodicals; Foie -- Maladies -- Périodiques; 616.362
• DOI: 10.1002/hep.29230
• Languages: English
• ISSNs: 0270-9139

Abstract

Abstract : Nonalcoholic steatohepatitis (NASH) is the most prevalent cause of chronic liver disease in the Western world. However, an optimum therapy for NASH is yet to be established, mandating more in‐depth investigation into the molecular pathogenesis of NASH to identify novel regulatory molecules and develop targeted therapies. Here, we unravel a unique function of astrocyte elevated gene‐1(AEG‐1)/metadherin in NASH using a transgenic mouse with hepatocyte‐specific overexpression of AEG‐1 (Alb/AEG‐1) and a conditional hepatocyte‐specific AEG‐1 knockout mouse (AEG‐1 ΔHEP ). Alb/AEG‐1 mice developed spontaneous NASH whereas AEG‐1 ΔHEP mice were protected from high‐fat diet (HFD)‐induced NASH. Intriguingly, AEG‐1 overexpression was observed in livers of NASH patients and wild‐type (WT) mice that developed steatosis upon feeding HFD. In‐depth molecular analysis unraveled that inhibition of peroxisome proliferator‐activated receptor alpha activity resulting in decreased fatty acid β‐oxidation, augmentation of translation of fatty acid synthase resulting in de novo lipogenesis, and increased nuclear factor kappa B–mediated inflammation act in concert to mediate AEG‐1‐induced NASH. Therapeutically, hepatocyte‐specific nanoparticle‐delivered AEG‐1 small interfering RNA provided marked protection from HFD‐induced NASH in WT mice. Conclusion : AEG‐1 might be a key molecule regulating initiation and progression of NASH. AEG‐1 inhibitory strategies might be developed as a potential therapeutic intervention in NASH patients. (Hepatology 2017;66:466–480).