Metabolic Profiling Reveals Aggravated Non-Alcoholic Steatohepatitis in High-Fat High-Cholesterol Diet-Fed Apolipoprotein E-Deficient Mice Lacking Ron Receptor Signaling

التفاصيل البيبلوغرافية
العنوان: Metabolic Profiling Reveals Aggravated Non-Alcoholic Steatohepatitis in High-Fat High-Cholesterol Diet-Fed Apolipoprotein E-Deficient Mice Lacking Ron Receptor Signaling
المؤلفون: T. Jake Liang, Jingwei Cai, Yuan Tian, Jingtao Zhang, Joselyn N. Allen, Yanling Ma, Adwitia Dey, Mary J. Kennett, Pamela A. Hankey-Giblin, Andrew D. Patterson
المصدر: Metabolites
Metabolites, Vol 10, Iss 326, p 326 (2020)
Volume 10
Issue 8
بيانات النشر: MDPI AG, 2020.
سنة النشر: 2020
مصطلحات موضوعية: 0301 basic medicine, Apolipoprotein E, medicine.medical_specialty, Endocrinology, Diabetes and Metabolism, lcsh:QR1-502, Inflammation, Biology, Biochemistry, lcsh:Microbiology, Article, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, lipid metabolism, medicine, macrophage stimulating protein (MSP), Receptor, Molecular Biology, mass spectrometry, Fatty liver, Lipid metabolism, medicine.disease, nuclear magnetic resonance, 030104 developmental biology, Endocrinology, Ron receptor tyrosine kinase, 030211 gastroenterology & hepatology, non-alcoholic steatohepatitis, Steatohepatitis, Steatosis, medicine.symptom, Tyrosine kinase
الوصف: Non-alcoholic steatohepatitis (NASH) represents the progressive sub-disease of non-alcoholic fatty liver disease that causes chronic liver injury initiated and sustained by steatosis and necroinflammation. The Ron receptor is a tyrosine kinase of the Met proto-oncogene family that potentially has a beneficial role in adipose and liver-specific inflammatory responses, as well as glucose and lipid metabolism. Since its discovery two decades ago, the Ron receptor has been extensively investigated for its differential roles on inflammation and cancer. Previously, we showed that Ron expression on tissue-resident macrophages limits inflammatory macrophage activation and promotes a repair phenotype, which can retard the progression of NASH in a diet-induced mouse model. However, the metabolic consequences of Ron activation have not previously been investigated. Here, we explored the effects of Ron receptor activation on major metabolic pathways that underlie the development and progression of NASH. Mice lacking apolipoprotein E (ApoE KO) and double knockout (DKO) mice that lack ApoE and Ron were maintained on a high-fat high-cholesterol diet for 18 weeks. We observed that, in DKO mice, the loss of ligand-dependent Ron signaling aggravated key pathological features in steatohepatitis, including steatosis, inflammation, oxidation stress, and hepatocyte damage. Transcriptional programs positively regulating fatty acid (FA) synthesis and uptake were upregulated in the absence of Ron receptor signaling, whereas lipid disposal pathways were downregulated. Consistent with the deregulation of lipid metabolism pathways, the DKO animals exhibited increased accumulation of FAs in the liver and decreased level of bile acids. Altogether, ligand-dependent Ron receptor activation provides protection from the deregulation of major metabolic pathways that initiate and aggravate non-alcoholic steatohepatitis.
وصف الملف: application/pdf
تدمد: 2218-1989
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00990b71bcdcbba27edcc2843a1ad7c2
https://doi.org/10.3390/metabo10080326
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....00990b71bcdcbba27edcc2843a1ad7c2
قاعدة البيانات: OpenAIRE