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Innate antiviral immunity and immunometabolism in hepatocytes
被引:3
|作者:
Sularea, Vasile Mihai
[1
]
Sugrue, Jamie A.
[1
]
O'Farrelly, Cliona
[1
,2
]
机构:
[1] Trinity Coll Dublin, Trinity Biomed Sci Inst, Sch Biochem & Immunol, Dublin, Ireland
[2] Trinity Coll Dublin, Sch Med, Dublin, Ireland
基金:
爱尔兰科学基金会;
关键词:
HEPATITIS-C-VIRUS;
FATTY LIVER-DISEASE;
DOUBLE-STRANDED-RNA;
RIG-I;
ENERGY-METABOLISM;
B-VIRUS;
ACTIVATION;
PROTEIN;
ALPHA;
CELLS;
D O I:
10.1016/j.coi.2022.102267
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
The human liver mediates whole-body metabolism, systemic inflammation and responses to hepatotropic pathogens. Hepatocytes, the most abundant cell type of the liver, have critical roles in each of these activities. The regulation of metabolic pathways, such as glucose metabolism, lipid biosynthesis and oxidation, influences whole-organism functionality. However, the immune potential of the liver in general and hepatocytes in particular is also determined by metabolic ability. The major shifts in cellular metabolism required to drive activity in immune cells are now welldescribed. Given the unique functions of hepatocytes in systemic metabolism and inflammation, and their ability to mediate local antiviral innate immunity, the metabolic shifts required to facilitate these activities are likely to be complex and challenging to define. In this review, we explore what is known about the complex metabolic rewiring required for hepatocytes to respond appropriately to viral infection. We also discuss how viruses can manipulate hepatocyte metabolism to facilitate infection.
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