Kupffer cells from halothane-exposed guinea pigs carry trifluoroacetylated protein adducts

Sylvia M. Furst, Dennis Luedke, A. Jay Gandolfi

Research output: Contribution to journalArticle

15 Scopus citations

Abstract

The anesthetic, halothane, is bioactivated by the liver cytochrome P450 system to trifluoroacetyl-chloride, which can readily acylate liver protein. Covalent binding of the trifluoroacetyl moiety may result in hapten formation leading to the induction of an immune response and ultimately halothane hepatitis. In this study the presence of trifluoroacetylated-protein adducts in Kupffer cells was investigated to learn how the immune system might come in contact with the proteins. Guinea pigs were exposed to 1.0% halothane, 40% oxygen for 4 h. Kupffer cells were isolated on days 1 through 9 post-exposure, by liver perfusion and purification by elutriation. Using gel electrophoresis and Western blotting techniques, it has been demonstrated that Kupffer cells obtained from halothane-treated guinea pigs, do carry trifluoroacetyl-protein adducts as recognized by an anti-trifluoroacetyl-rabbit serum albumin antibody. Apparent molecular weights of polypeptides bound by trifluoroacetyl were of a wide range, 25-152 kDa. Bands were most prominent in the larger Kupffer cells with more appearing at lower molecular weights. Trifluoroacetyl-protein adducts were not detected in lung, spleen, lymph node or peripheral blood macrophages. This work suggests a role for Kupffer cells in the presentation of altered proteins in the liver to cells of the immune system.

Original languageEnglish (US)
Pages (from-to)119-132
Number of pages14
JournalToxicology
Volume120
Issue number2
DOIs
StatePublished - Jun 27 1997

Keywords

  • Antigen presenting cell
  • Halothane (2-bromo-2-chloro-1,1,1-trifluoroethane)
  • Hepatotoxicity
  • Immunochemistry
  • Kupffer cell
  • Trifluoroacetylated-adduct

ASJC Scopus subject areas

  • Toxicology

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