An Early Complement-Dependent and TLR-4-Independent Phase in the Pathogenesis of Ethanol-Induced Liver Injury in Mice

被引:88
作者
Roychowdhury, Sanjoy
McMullen, Megan R.
Pritchard, Michele T.
Hise, Amy G.
van Rooijen, Nico [3 ]
Medof, M. Edward [4 ]
Stavitsky, Abram B. [5 ]
Nagy, Laura E. [1 ,2 ,6 ]
机构
[1] Cleveland Clin Fdn, Dept Pathobiol, Lerner Res Inst NE40, Cleveland, OH 44195 USA
[2] Cleveland Clin Fdn, Dept Gastroenterol, Cleveland, OH 44195 USA
[3] Cleveland Clin Fdn, Dept Gastroenterol, Cleveland, OH 44195 USA
[4] Case Western Reserve Univ, Dept Pathol, Cleveland, OH 44106 USA
[5] Case Western Reserve Univ, Dept Mol Biol & Microbiol, Cleveland, OH 44106 USA
[6] Case Western Reserve Univ, Dept Nutr, Cleveland, OH 44106 USA
基金
美国国家卫生研究院;
关键词
KUPFFER CELLS; CUTTING EDGE; IN-VIVO; RECEPTOR; EXPRESSION; C5A; ACTIVATION; C3; MECHANISMS; RAT;
D O I
10.1002/hep.22776
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The innate immune system has been implicated in the pathogenesis of alcoholic liver disease. Although innate immunity is usually considered an early response to injury, previous work implicating innate immunity in ethanol-induced liver injury focuses primarily on long-term ethanol exposure. We investigated the early period of ethanol exposure to determine whether there were temporal associations between activation of innate immune responses and known correlates of liver injury. Female C57BL/6 mice were allowed free access to an ethanol-containing Lieber-DeCarli diet or were pair-fed a control diet. Within 4 days of ethanol exposure, we observed a striking spike in expression of hepatic proinflammatory cytokines-including tumor necrosis factor alpha (TNF-alpha), interleukin-6, and interferon-gamma-prior to hepatic triglyceride accumulation or increased plasma alanine aminotransferase activities, as well as before the induction of cytochrome P450 2E1 or oxidative stress. This early spike in inflammatory cytokines coincided with deposition of C3b-iC3b/C3c (C3b) in the liver. This deposition, resulting from the cleavage of the third component of the complement system (0), is evidence for activation of complement in response to ethanol. C3(-/-) mice were protected from the early, ethanol-induced increase in hepatic TNF-alpha expression. Ethanol increased Ob deposition in mice deficient in C3a receptor or C5a receptor, as well as in wild-type mice depleted of hepatic macrophages; however, there was no increase in hepatic TNF-alpha in the absence of C3a receptor, C5a receptor, or hepatic macrophages. In contrast, the absence of Toll-like receptor 4 (TLR-4) had no effect on the early, ethanol-induced increase in either Ob or TNF-alpha. Conclusion: We have identified a complement- and macrophage-dependent, but TLR-4 independent, phase in the pathogenesis of ethanol-induced liver injury. (HEPATOLOGY 2009;49:1326-1334.)
引用
收藏
页码:1326 / 1334
页数:9
相关论文
共 30 条
[11]  
Hoshino K, 1999, J IMMUNOL, V162, P3749
[12]   Generation of C5a in the absence of C3: a new complement activation pathway [J].
Huber-Lang, Markus ;
Sarma, J. Vidya ;
Zetoune, Firas S. ;
Rittirsch, Daniel ;
Neff, Thomas A. ;
McGuire, Stephanie R. ;
Lambris, John D. ;
Warner, Roscoe L. ;
Flierl, Michael A. ;
Hoesel, Laszlo M. ;
Gebhard, Florian ;
Younger, John G. ;
Drouin, Scott M. ;
Wetsel, Rick A. ;
Ward, Peter A. .
NATURE MEDICINE, 2006, 12 (06) :682-687
[13]   A role for the C3a anaphylatoxin receptor in the effector phase of asthma [J].
Humbles, AA ;
Lu, B ;
Nilsson, CA ;
Lilly, C ;
Israel, E ;
Fujiwara, Y ;
Gerard, NP ;
Gerard, C .
NATURE, 2000, 406 (6799) :998-1001
[14]   Activation of complement components and reduced regulator expression in alcohol-induced liver injury in the rat [J].
Järveläinen, HA ;
Väkevä, A ;
Lindros, KO ;
Meri, S .
CLINICAL IMMUNOLOGY, 2002, 105 (01) :57-63
[15]   Complement component anaphylatoxins upregulate chemokine expression by human astrocytes [J].
Jauneau, AC ;
Ischenko, A ;
Chan, P ;
Fontaine, M .
FEBS LETTERS, 2003, 537 (1-3) :17-22
[16]   Cutting edge: Targeted disruption of the C3a receptor gene demonstrates a novel protective anti-inflammatory role for C3a in endotoxin-shock [J].
Kildsgaard, J ;
Hollmann, TJ ;
Matthews, KW ;
Bian, K ;
Murad, F ;
Wetsel, RA .
JOURNAL OF IMMUNOLOGY, 2000, 165 (10) :5406-5409
[17]   Cell-derived anaphylatoxins as key mediators of anti body-dependent type II autoimmunity in mice [J].
Kumar, V ;
Ali, SR ;
Konrad, S ;
Zwirner, J ;
Verbeek, JS ;
Schmidt, RE ;
Gessner, JE .
JOURNAL OF CLINICAL INVESTIGATION, 2006, 116 (02) :512-520
[18]   The role of complement in inflammatory diseases from behind the scenes into the spotlight [J].
Markiewski, Maciej M. ;
Lambris, John D. .
AMERICAN JOURNAL OF PATHOLOGY, 2007, 171 (03) :715-727
[19]   Novel monoclonal antibodies against mouse C3 interfering with complement activation:: description of fine specificity and applications to various immunoassays [J].
Mastellos, D ;
Prechl, J ;
László, G ;
Papp, K ;
Oláh, E ;
Argyropoulos, E ;
Franchini, S ;
Tudoran, R ;
Markiewski, M ;
Lambris, JD ;
Erdei, A .
MOLECULAR IMMUNOLOGY, 2004, 40 (16) :1213-1221
[20]   Chronic ethanol exposure increases the binding of HuR to the TNFα 3′-untranslated region in macrophages [J].
McMullen, MR ;
Cocuzzi, E ;
Hatzoglou, M ;
Nagy, LE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (40) :38333-38341