Human Microsomal Epoxide Hydrolase Is the Target of Germander-Induced Autoantibodies on the Surface of Human Hepatocytes
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...
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Veröffentlicht in: | Molecular pharmacology 2000-09, Vol.58 (3), p.542-551 |
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creator | De Berardinis, V Moulis, C Maurice, M Beaune, P Pessayre, D Pompon, D Loeper, J |
description | 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 cytochrome b 5 in a âhumanizedâ 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. |
doi_str_mv | 10.1124/mol.58.3.542 |
format | Article |
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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 cytochrome b 5 in a âhumanizedâ 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.</description><identifier>ISSN: 0026-895X</identifier><identifier>EISSN: 1521-0111</identifier><identifier>DOI: 10.1124/mol.58.3.542</identifier><identifier>PMID: 10953047</identifier><language>eng</language><publisher>United States: American Society for Pharmacology and Experimental Therapeutics</publisher><subject>Alkylation ; Autoantibodies - drug effects ; Autoantibodies - immunology ; Diterpenes - immunology ; Diterpenes - metabolism ; Diterpenes - pharmacology ; Epoxide Hydrolases - antagonists & inhibitors ; Epoxide Hydrolases - genetics ; Epoxide Hydrolases - immunology ; Humans ; Liver - cytology ; Liver - drug effects ; Liver - enzymology ; Microsomes - drug effects ; Microsomes - enzymology ; Plant Extracts - pharmacology ; Plants, Medicinal - chemistry ; Precipitin Tests ; Saccharomyces cerevisiae - genetics ; Spiro Compounds - immunology ; Spiro Compounds - metabolism ; Spiro Compounds - pharmacology ; Teucrium ; Transfection</subject><ispartof>Molecular pharmacology, 2000-09, Vol.58 (3), p.542-551</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c383t-77d1024d0d7c7b7641f9f994b11499140518054c05428a50833f6bf0cf055593</citedby><cites>FETCH-LOGICAL-c383t-77d1024d0d7c7b7641f9f994b11499140518054c05428a50833f6bf0cf055593</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10953047$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>De Berardinis, V</creatorcontrib><creatorcontrib>Moulis, C</creatorcontrib><creatorcontrib>Maurice, M</creatorcontrib><creatorcontrib>Beaune, P</creatorcontrib><creatorcontrib>Pessayre, D</creatorcontrib><creatorcontrib>Pompon, D</creatorcontrib><creatorcontrib>Loeper, J</creatorcontrib><title>Human Microsomal Epoxide Hydrolase Is the Target of Germander-Induced Autoantibodies on the Surface of Human Hepatocytes</title><title>Molecular pharmacology</title><addtitle>Mol Pharmacol</addtitle><description>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 cytochrome b 5 in a âhumanizedâ 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.</description><subject>Alkylation</subject><subject>Autoantibodies - drug effects</subject><subject>Autoantibodies - immunology</subject><subject>Diterpenes - immunology</subject><subject>Diterpenes - metabolism</subject><subject>Diterpenes - pharmacology</subject><subject>Epoxide Hydrolases - antagonists & inhibitors</subject><subject>Epoxide Hydrolases - genetics</subject><subject>Epoxide Hydrolases - immunology</subject><subject>Humans</subject><subject>Liver - cytology</subject><subject>Liver - drug effects</subject><subject>Liver - enzymology</subject><subject>Microsomes - drug effects</subject><subject>Microsomes - enzymology</subject><subject>Plant Extracts - pharmacology</subject><subject>Plants, Medicinal - chemistry</subject><subject>Precipitin Tests</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>Spiro Compounds - immunology</subject><subject>Spiro Compounds - metabolism</subject><subject>Spiro Compounds - pharmacology</subject><subject>Teucrium</subject><subject>Transfection</subject><issn>0026-895X</issn><issn>1521-0111</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkEFP3DAQha0KVLbAjTPyBU7NduzYm_iIELArUfXQPfRmOfZ4NyiJg50I9t-TbZDaw2gu33tP-gi5YrBkjIsfbWiWslzmSyn4F7JgkrMMGGMnZAHAV1mp5J8z8i2lFwAmZAlfyRkDJXMQxYK8r8fWdPRnbWNIoTUNfejDe-2Qrg8uhsYkpJtEhz3SrYk7HGjw9AnjFHIYs03nRouO3o1DMN1QV8HVmGjo_iZ-j9Ebi8fIPLPG3gzBHgZMF-TUmybh5ec_J9vHh-39Onv-9bS5v3vObF7mQ1YUjgEXDlxhi6pYCeaVV0pUjAmlmADJSpDCTsdLI6HMc7-qPFgPUkqVn5PbubaP4XXENOi2ThabxnQYxqQLzkEofgS_z-BRRIrodR_r1sSDZqCPovUkWstS53qamvDrz96xatH9B89mJ-BmBvb1bv9WR9T93kzabGjC7vCv6AN5q4Yo</recordid><startdate>20000901</startdate><enddate>20000901</enddate><creator>De Berardinis, V</creator><creator>Moulis, C</creator><creator>Maurice, M</creator><creator>Beaune, P</creator><creator>Pessayre, D</creator><creator>Pompon, D</creator><creator>Loeper, J</creator><general>American Society for Pharmacology and Experimental Therapeutics</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20000901</creationdate><title>Human Microsomal Epoxide Hydrolase Is the Target of Germander-Induced Autoantibodies on the Surface of Human Hepatocytes</title><author>De Berardinis, V ; Moulis, C ; Maurice, M ; Beaune, P ; Pessayre, D ; Pompon, D ; Loeper, J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c383t-77d1024d0d7c7b7641f9f994b11499140518054c05428a50833f6bf0cf055593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Alkylation</topic><topic>Autoantibodies - drug effects</topic><topic>Autoantibodies - immunology</topic><topic>Diterpenes - immunology</topic><topic>Diterpenes - metabolism</topic><topic>Diterpenes - pharmacology</topic><topic>Epoxide Hydrolases - antagonists & inhibitors</topic><topic>Epoxide Hydrolases - genetics</topic><topic>Epoxide Hydrolases - immunology</topic><topic>Humans</topic><topic>Liver - cytology</topic><topic>Liver - drug effects</topic><topic>Liver - enzymology</topic><topic>Microsomes - drug effects</topic><topic>Microsomes - enzymology</topic><topic>Plant Extracts - pharmacology</topic><topic>Plants, Medicinal - chemistry</topic><topic>Precipitin Tests</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>Spiro Compounds - immunology</topic><topic>Spiro Compounds - metabolism</topic><topic>Spiro Compounds - pharmacology</topic><topic>Teucrium</topic><topic>Transfection</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>De Berardinis, V</creatorcontrib><creatorcontrib>Moulis, C</creatorcontrib><creatorcontrib>Maurice, M</creatorcontrib><creatorcontrib>Beaune, P</creatorcontrib><creatorcontrib>Pessayre, D</creatorcontrib><creatorcontrib>Pompon, D</creatorcontrib><creatorcontrib>Loeper, J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>De Berardinis, V</au><au>Moulis, C</au><au>Maurice, M</au><au>Beaune, P</au><au>Pessayre, D</au><au>Pompon, D</au><au>Loeper, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Human Microsomal Epoxide Hydrolase Is the Target of Germander-Induced Autoantibodies on the Surface of Human Hepatocytes</atitle><jtitle>Molecular pharmacology</jtitle><addtitle>Mol Pharmacol</addtitle><date>2000-09-01</date><risdate>2000</risdate><volume>58</volume><issue>3</issue><spage>542</spage><epage>551</epage><pages>542-551</pages><issn>0026-895X</issn><eissn>1521-0111</eissn><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 cytochrome b 5 in a âhumanizedâ 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.</abstract><cop>United States</cop><pub>American Society for Pharmacology and Experimental Therapeutics</pub><pmid>10953047</pmid><doi>10.1124/mol.58.3.542</doi><tpages>10</tpages></addata></record> |
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source | MEDLINE; EZB Free E-Journals; Free Full-Text Journals in Chemistry |
subjects | Alkylation Autoantibodies - drug effects Autoantibodies - immunology Diterpenes - immunology Diterpenes - metabolism Diterpenes - pharmacology Epoxide Hydrolases - antagonists & inhibitors Epoxide Hydrolases - genetics Epoxide Hydrolases - immunology Humans Liver - cytology Liver - drug effects Liver - enzymology Microsomes - drug effects Microsomes - enzymology Plant Extracts - pharmacology Plants, Medicinal - chemistry Precipitin Tests Saccharomyces cerevisiae - genetics Spiro Compounds - immunology Spiro Compounds - metabolism Spiro Compounds - pharmacology Teucrium Transfection |
title | Human Microsomal Epoxide Hydrolase Is the Target of Germander-Induced Autoantibodies on the Surface of Human Hepatocytes |
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