Human Microsomal Epoxide Hydrolase Is the Target of Germander-Induced Autoantibodies on the Surface of Human Hepatocytes
- Veronique De Berardinis1,
- Claude Moulis2,
- Michele Maurice3,
- Philippe Beaune4,
- Dominique Pessayre5,
- Denis Pompon1 and
- Jacqueline Loeper1
- 1Centre de Génétique Moléculaire du Centre National de la Recherche Scientifique, Laboratoire propre associéà l'Université Pierre et Marie Curie, Gif-sur-Yvette (V.D.B., D.Po., J.L.); 2Laboratoire de Pharmacognosie, UniversitéToulouse III (C.M.); 3de l'Institut National de la Santé et de la Recherche Médicale:Unité 538, UniversitéSaint-Antoine, Paris (M.M.); 4Unité 490, Université Paris V (P.B.); and 5Unité 481, Hôpital Beaujon, Clichy, France (D.Pe.)
Abstract
Germander, a plant used in folk medicine, caused an epidemic of cytolytic hepatitis in France. In about half of these patients, a rechallenge caused early recurrence, suggesting an immunoallergic type of hepatitis. Teucrin A (TA) was found responsible for the hepatotoxicity via metabolic activation by CYP3A. In this study, we describe the presence of anti-microsomal epoxide hydrolase (EH) autoantibodies in the sera of patients who drank germander teas for a long period of time. By Western blotting and immunocytochemistry, human microsomal EH was shown to be present in purified plasma membranes of both human hepatocytes and transformed spheroplasts and to be exposed on the cell surface where affinity-purified germander autoantibodies recognized it as their autoantigen. Immunoprecipitation of EH activity by germander-induced autoantibodies confirmed this finding. These autoantibodies were not immunoinhibitory. The plasma membrane-located EH was catalytically competent and may act as target for reactive metabolites from TA. To test this hypothesis CYP3A4 and EH were expressed with human cytochrome P450 reductase and cytochromeb5 in a “humanized” yeast strain. In the absence of EH only one metabolite was formed. In the presence of EH, two additional metabolites were formed, and a time-dependent inactivation of EH was detected, suggesting that a reactive oxide derived from TA could alkylate the enzyme and trigger an immune response. Antibodies were found to recognize TA-alkykated EH. Recognition of EH present at the surface of human hepatocytes could suggest an (auto)antibody participation in an immune cell destruction.
Footnotes
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Send reprint requests to: Jacqueline Loeper, Pharm. D., Ph.D., Centre de Génétique Moléculaire du Centre National de la Recherche Scientifique, F91198 Gif-sur-Yvette Cedex, France. E-mail: loeper{at}cgm.cnrs-gif.fr
- Abbreviations:
- CYP
- cytochrome P450
- TA
- teucrin A
- EH
- epoxide hydrolase
- hmEH
- human microsomal epoxide hydrolase
- PM
- plasma membrane
- GIAA
- germander-induced autoantibodies
- CPR
- NADPH-cytochrome P450-reductase
- GAPDH
- glyceraldehyde-3-phosphate dehydrogenase
- PCR
- polymerase chain reaction
- bp
- base pair
- PAGE
- polyacrylamide gel electrophoresis
- B(a)P
- Benzo(a)pyrene
- MHC
- major histocompatibility complex
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- Received January 19, 2000.
- Accepted June 6, 2000.
- The American Society for Pharmacology and Experimental Therapeutics



