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Publication : Regulatory Role of Endothelial PHD2 in the Hepatic Steatosis.

First Author  Zhou LY Year  2018
Journal  Cell Physiol Biochem Volume  48
Issue  3 Pages  1003-1011
PubMed ID  30036883 Mgi Jnum  J:304486
Mgi Id  MGI:6514461 Doi  10.1159/000491968
Citation  Zhou LY, et al. (2018) Regulatory Role of Endothelial PHD2 in the Hepatic Steatosis. Cell Physiol Biochem 48(3):1003-1011
abstractText  BACKGROUND/AIMS: Liver disease is a leading cause of high mortality and morbidity worldwide. The aim of the present study is to investigate the regulatory role of prolyl hydroxylase-2 (PHD2)-hypoxia-inducible factor-2a (HIF-2alpha) axis on nonalcoholic fatty liver disease (NAFLD) and to explore the potential mechanisms by which endothelial (EC)-specific PHD2 deficiency regulates hepatic steatosis and fibrosis. METHODS: In the endothelial-specific PHD2 knockout (PHD2ECKO) mouse fed with normal diet or high fat diet (HFD), liver lipid accumulation and fibrosis were measured by Oil Red O and Masson trichrome staining. The fat and body weight (FW/BW) ratio and glucose tolerance were measured. The expression of HIF-2alpha, atrial natriuretic peptide (ANP), angiopoietin-2 (Ang-2), and transforming growth factor-b (TGF-beta) were analyzed by western blot analysis. RESULTS: The steatosis and fibrosis were significantly increased in the PHD2ECKO mice. FW/BW ratio was significantly increased in the PHD2ECKO mice. Moreover, knockout of endothelial PHD2 resulted in an impairment of glucose tolerance in mice. Western blot analysis showed that the expression of HIF-2alpha in liver tissues was not significantly increased. Interestingly, the expression of ANP was decreased, and Ang-2 and TGF-beta levels were significantly increased in the liver of PHD2ECKO mice. The FW/BW ratio was also significantly increased in the PHD2ECKO mice fed with HFD for 16 weeks. Feeding HFD resulted in a significant increase in hepatic steatosis in the control PHD2f/f mice, but did not further enhance hepatic steatosis in the PHD2ECKO mice. CONCLUSIONS: We concluded that the endothelial PHD2 plays a critical role in hepatic steatosis and fibrosis, which may be involved in the regulation of ANP and Ang-2/TGF-beta signaling pathway, but not the HIF-2alpha expression.
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