Role of Toll-Like Receptors and Their Downstream Molecules in the Development of Nonalcoholic Fatty Liver Disease

被引:124
作者
Miura, Kouichi [1 ]
Seki, Ekihiro [2 ]
Ohnishi, Hirohide [1 ]
Brenner, David A. [2 ]
机构
[1] Akita Univ, Grad Sch Med, Dept Gastroenterol & Neurol, Akita 0108543, Japan
[2] Univ Calif San Diego, Dept Med, Sch Med, La Jolla, CA 92093 USA
关键词
TOTAL PARENTERAL-NUTRITION; NECROSIS-FACTOR-ALPHA; MONOCYTE CHEMOATTRACTANT PROTEIN-1; INDUCED HEPATIC STEATOSIS; INSULIN-RESISTANCE; KUPFFER CELLS; GUT MICROBIOTA; ADIPOSE-TISSUE; LIPID-ACCUMULATION; INNATE IMMUNITY;
D O I
10.1155/2010/362847
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Activation of innate immunity is associated with the development of liver disease, including non-alcoholic fatty liver disease (NAFLD). In the innate immune system, Toll-like receptors (TLRs) are sensors that recognize bacterial and viral components such as lipopolysaccharide, bacterial DNA, and peptidoglycan. Recent data have demonstrated that the liver is exposed to a high load of TLR ligands due to bacterial overgrowth and increased intestinal permeability in NAFLD. Upon stimulation by these TLR ligands, hepatic immune cells produce various mediators that are involved in host defense. On the other hand, these mediators alter lipid metabolism, insulin signaling, and cell survival. Indeed, some TLR-deficient mice demonstrate lesser degrees of NAFLD even though TLR ligands are increased. This paper will highlight the recent progress on the study of TLR signaling and their downstream molecules in the development of NAFLD.
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页数:9
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