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Multifaceted Interaction Between Hepatitis B Virus Infection and Lipid Metabolism in Hepatocytes: A Potential Target of Antiviral Therapy for Chronic Hepatitis B

期刊

FRONTIERS IN MICROBIOLOGY
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fmicb.2021.636897

关键词

hepatitis B virus; chronic hepatitis B; lipid metabolism; apolipoprotein; hepatic steatosis; metabolic signaling pathway; nuclear factors

资金

  1. National Natural Science Foundation of China [81772198]
  2. National Science and Technology Major Project of China [2017ZX10202203, 2018ZX10302206]
  3. Natural Science Foundation of Chongqing, China [cstc2020jcyj-msxmX0389]

向作者/读者索取更多资源

Hepatitis B virus (HBV) is considered a metabolic virus affecting hepatic metabolic pathways, but its impact on lipid metabolism in hepatocytes is still uncertain. Clinical studies suggest that chronic HBV infection is associated with lower levels of cholesterol and triglycerides and a lower prevalence of hepatic steatosis compared to non-infected controls. Various mechanisms of how HBV affects hepatic lipid metabolism have been explored, showing changes in lipogenesis, cholesterolgenesis, fatty acid oxidation, and bile acid synthesis. Further research is needed to fully understand the complex interaction between HBV infection and hepatic lipid metabolism.
Hepatitis B virus (HBV) is considered a metabolic virus and affects many hepatic metabolic pathways. However, how HBV affects lipid metabolism in hepatocytes remains uncertain yet. Accumulating clinical studies suggested that compared to non-HBV-infected controls, chronic HBV infection was associated with lower levels of serum total cholesterol and triglycerides and a lower prevalence of hepatic steatosis. In patients with chronic HBV infection, high ALT level, high body mass index, male gender, or old age was found to be positively correlated with hepatic steatosis. Furthermore, mechanisms of how HBV infection affected hepatic lipid metabolism had also been explored in a number of studies based on cell lines and mouse models. These results demonstrated that HBV replication or expression induced extensive and diverse changes in hepatic lipid metabolism, by not only activating expression of some critical lipogenesis and cholesterolgenesis-related proteins but also upregulating fatty acid oxidation and bile acid synthesis. Moreover, increasing studies found some potential targets to inhibit HBV replication or expression by decreasing or enhancing certain lipid metabolism-related proteins or metabolites. Therefore, in this article, we comprehensively reviewed these publications and revealed the connections between clinical observations and experimental findings to better understand the interaction between hepatic lipid metabolism and HBV infection. However, the available data are far from conclusive, and there is still a long way to go before clarifying the complex interaction between HBV infection and hepatic lipid metabolism.

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