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
相关论文
共 103 条
[1]   Mouse models in non-alcoholic fatty liver disease and steatohepatitis research [J].
Anstee, QM ;
Goldin, RD .
INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY, 2006, 87 (01) :1-16
[2]   Autocrine loop between TGF-β1 and IL-1β through Smad3- and ERK-dependent pathways in rat pancreatic stellate cells [J].
Aoki, H ;
Ohnishi, H ;
Hama, K ;
Ishijima, T ;
Satoh, Y ;
Hanatsuka, K ;
Ohashi, A ;
Wada, S ;
Miyata, T ;
Kita, H ;
Yamamoto, H ;
Osawa, H ;
Sato, K ;
Tamada, K ;
Yasuda, H ;
Mashima, H ;
Sugano, K .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2006, 290 (04) :C1100-C1108
[3]   IKK-β links inflammation to obesity-induced insulin resistance [J].
Arkan, MC ;
Hevener, AL ;
Greten, FR ;
Maeda, S ;
Li, ZW ;
Long, JM ;
Wynshaw-Boris, A ;
Poli, G ;
Olefsky, J ;
Karin, M .
NATURE MEDICINE, 2005, 11 (02) :191-198
[4]   The gut microbiota as an environmental factor that regulates fat storage [J].
Bäckhed, F ;
Ding, H ;
Wang, T ;
Hooper, LV ;
Koh, GY ;
Nagy, A ;
Semenkovich, CF ;
Gordon, JI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (44) :15718-15723
[5]   Kupffer cells in non-alcoholic fatty liver disease: The emerging view [J].
Baffy, Gyoergy .
JOURNAL OF HEPATOLOGY, 2009, 51 (01) :212-223
[6]   Infliximab reverses steatosis and improves insulin signal transduction in liver of rats fed a high-fat diet [J].
Barbuio, Raquel ;
Milanski, Marciane ;
Bertolo, Manoel B. ;
Saad, Mario J. ;
Velloso, Licio A. .
JOURNAL OF ENDOCRINOLOGY, 2007, 194 (03) :539-550
[7]   Prevalence of and risk factors for hepatic steatosis in northern Italy [J].
Bellentani, S ;
Saccoccio, G ;
Masutti, F ;
Crocè, LS ;
Brandi, G ;
Sasso, F ;
Cristanini, G ;
Tiribelli, C .
ANNALS OF INTERNAL MEDICINE, 2000, 132 (02) :112-117
[8]   Role of Kupffer cells in host defense and liver disease [J].
Bilzer, Manfred ;
Roggel, Frigga ;
Gerbes, Alexander L. .
LIVER INTERNATIONAL, 2006, 26 (10) :1175-1186
[9]   Reduced atherosclerosis in MyD88-null mice links elevated serum cholesterol levels to activation of innate immunity signaling pathways [J].
Björkbacka, H ;
Kunjathoor, VV ;
Moore, KJ ;
Koehn, S ;
Ordija, CM ;
Lee, MA ;
Means, T ;
Halmen, K ;
Luster, AD ;
Golenbock, DT ;
Freeman, MW .
NATURE MEDICINE, 2004, 10 (04) :416-421
[10]  
Bradbury Michael W, 2004, Clin Liver Dis, V8, P639, DOI 10.1016/j.cld.2004.04.005