Scientific Reports · 2015 · 87 citations · 44 references
Life SciencesBiochemistryMolecular BiologyGene ExpressionInflammationMetabolismAdipose TissueBiomarkers Of Liver InjuryHepatic PathophysiologyLipid MetabolismLiver DiseaseMetabolic DiseaseActivated Hepatic Stellate CellsAdipose Tissue BiomarkersKupffer CellsMetabolic Disease BiomarkersOxidative Stress InjurySteatosis BiomarkersTherapeutic Target IdentificationWhite Adipose Tissue Biology
Nonalcoholic fatty liver disease (NAFLD) is the most common cause of chronic liver disease worldwide. Gpnmb is classified as a type 1 membrane protein and its soluble form is secreted by ADAM10-mediated cleavage. Gpnmb mRNA was found in the Kupffer cells and white adipose tissues (WATs) and its upregulation in obesity was recently found. Here, we generated aP2 promoter-driven Gpnmb transgenic (Tg) mice and the overexpression of Gpnmb ameliorated the fat accumulation and fibrosis of the liver in diet-induced obesity model. Soluble form of Gpnmb in sera was elevated in Gpnmb Tg mice and Gpnmb concentrated in hepatic macrophages and stellate cells interacted with calnexin, which resulted in the reduction of oxidative stress. In the patients with non-alcoholic steatohepatitis, serum soluble GPNMB concentrations were higher compared with the patients with simple steatosis. The GPNMB is a promising biomarker and therapeutic target for the development and progression of NAFLD in obesity.
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Design and validation of a histological scoring system for nonalcoholic fatty liver disease†
David E. Kleiner, Elizabeth M. Brunt, Mark L. Van Natta et al. · Hepatology · 2005 · 10.7K citations
Nonalcoholic fatty liver disease: A spectrum of clinical and pathological severity☆, ☆☆
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Naga Chalasani, Zobair M. Younossi, Joel E. Lavine et al. · Gastroenterology · 2012 · 1.8K citations · Full text