Differential contributions of C3, C5, and decay-accelerating factor to ethanol-induced fatty liver in mice

Gastroenterology. 2007 Mar;132(3):1117-1126. doi: 10.1053/j.gastro.2007.01.053. Epub 2007 Feb 1.

Abstract

Background and aims: The complement pathway is an important component of the innate and adaptive immune response. Here we tested the hypothesis that activation of complement is required for development of ethanol-induced fatty liver.

Methods: Wild-type mice and mice lacking the third (C3) or fifth (C5) components of the complement activation pathway, as well as mice lacking decay-accelerating factor (CD55/DAF), a complement regulatory protein, were fed Lieber-DeCarli ethanol-containing diets for 6 weeks or pair-fed control diets.

Results: Ethanol feeding to wild-type mice increased C3a in plasma. Wild-type and C5-/- mice fed the ethanol diet developed hepatic steatosis characterized by microvesicular and macrovesicular lipid accumulation and increased triglyceride content. C3-/- mice did not develop steatosis, while CD55/DAF-/- mice accumulated even more hepatic triglyceride after ethanol feeding than wild-type mice. Levels of serum alanine aminotransferase and hepatic tumor necrosis factor alpha, indicators of hepatocyte injury and inflammation, respectively, were increased in wild-type and CD55/DAF-/- mice but not in C5-/- mice after ethanol feeding. In contrast to the protective effect of C3-/- against ethanol-induced steatosis, levels of both alanine aminotransferase and tumor necrosis factor alpha were increased in C3-/- mice after ethanol feeding.

Conclusions: Here we have identified several elements of the complement system as important contributors to ethanol-induced fatty liver. C3 contributed primarily to the accumulation of triglyceride in the liver, whereas C5 was involved in inflammation and injury to hepatocytes. Further, the absence of CD55/DAF exacerbated these responses, suggesting that CD55/DAF serves as a barrier to ethanol-induced fatty liver.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Alanine Transaminase / blood
  • Animals
  • CD55 Antigens / genetics
  • CD55 Antigens / metabolism*
  • Central Nervous System Depressants / blood
  • Complement C3 / deficiency
  • Complement C3 / genetics
  • Complement C3 / metabolism*
  • Complement C3a / metabolism
  • Complement C5 / deficiency
  • Complement C5 / genetics
  • Complement C5 / metabolism*
  • Cytochrome P-450 CYP2E1 / biosynthesis
  • Disease Models, Animal
  • Enzyme Induction
  • Ethanol / blood
  • Fatty Liver, Alcoholic / etiology
  • Fatty Liver, Alcoholic / metabolism*
  • Fatty Liver, Alcoholic / pathology
  • Female
  • Interferon-gamma / metabolism
  • Interleukin-6 / metabolism
  • Liver / enzymology
  • Liver / metabolism*
  • Liver / pathology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Triglycerides / metabolism
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • CD55 Antigens
  • Central Nervous System Depressants
  • Complement C3
  • Complement C5
  • Interleukin-6
  • Triglycerides
  • Tumor Necrosis Factor-alpha
  • Ethanol
  • Complement C3a
  • Interferon-gamma
  • Cytochrome P-450 CYP2E1
  • Alanine Transaminase