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The Role of Thiols in Mitochondrial Susceptibility to Iron and tert-Butyl Hydroperoxide-Mediated Toxicity in Cultured Mouse Hepatocytes
Cultured hepatocytes derived from the newborn mutant c14CoS/c14CoS mouse (14CoS/14CoS cells) have 3-fold higher levels of reduced glutathione (GSH) and greater resistance to menadione toxicity than hepatocytes derived from the wild-type cch/cch mouse (ch/ch cells). Therefore, we used these cell line...
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Published in: | Chemical research in toxicology 1994-05, Vol.7 (3), p.358-366 |
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creator | Shertzer, Howard G Bannenberg, Gerard L Zhu, Huan Liu, Rui-Ming Moldeus, Peter |
description | Cultured hepatocytes derived from the newborn mutant c14CoS/c14CoS mouse (14CoS/14CoS cells) have 3-fold higher levels of reduced glutathione (GSH) and greater resistance to menadione toxicity than hepatocytes derived from the wild-type cch/cch mouse (ch/ch cells). Therefore, we used these cell lines to examine mechanisms of oxidative stress produced by iron and tert-butyl hydroperoxide (TBHP). Both cell types were resistant to 25 microM Fe2+ toxicity in the absence of added TBHP. However, in the presence of Fe2+, striking differences in susceptibility to TBHP toxicity between the cell types were observed. With 25 microM Fe2+, ch/ch cells showed TBHP concentration-dependent toxicity, with total lethality at 500 microM; in contrast, 14CoS/14CoS cells were completely resistant to the lethal effects of this concentration of TBHP. Concentration-dependent TBHP-mediated increases in cytosolic Ca2+, pH, and GSSG/GSH ratios, and decreases in GSH levels, were evident in ch/ch cells. 14CoS/14CoS cells exhibited concentration-dependent TBHP-mediated changes in GSH and GSSG/GSH ratios, but cytosolic Ca2+ and pH remained at control levels. Mitochondrial GSH pools were also diminished by TBHP, although there was no selective depletion; mitochondrial GSH remained at about 14% of total cellular GSH. Both cell types exhibited the same time-dependent decrease in plasma membrane protein thiols and a time-dependent increase in plasma membrane protein carbonyls. However, only ch/ch cells displayed a time-dependent depletion of mitochondrial protein thiols, concomitant with an increase in mitochondrial protein carbonyls, while 14CoS/14CoS cells were resistant to such changes. All of the effects produced by TBHP were prevented by desferoxamine. |
doi_str_mv | 10.1021/tx00039a013 |
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Therefore, we used these cell lines to examine mechanisms of oxidative stress produced by iron and tert-butyl hydroperoxide (TBHP). Both cell types were resistant to 25 microM Fe2+ toxicity in the absence of added TBHP. However, in the presence of Fe2+, striking differences in susceptibility to TBHP toxicity between the cell types were observed. With 25 microM Fe2+, ch/ch cells showed TBHP concentration-dependent toxicity, with total lethality at 500 microM; in contrast, 14CoS/14CoS cells were completely resistant to the lethal effects of this concentration of TBHP. Concentration-dependent TBHP-mediated increases in cytosolic Ca2+, pH, and GSSG/GSH ratios, and decreases in GSH levels, were evident in ch/ch cells. 14CoS/14CoS cells exhibited concentration-dependent TBHP-mediated changes in GSH and GSSG/GSH ratios, but cytosolic Ca2+ and pH remained at control levels. Mitochondrial GSH pools were also diminished by TBHP, although there was no selective depletion; mitochondrial GSH remained at about 14% of total cellular GSH. Both cell types exhibited the same time-dependent decrease in plasma membrane protein thiols and a time-dependent increase in plasma membrane protein carbonyls. However, only ch/ch cells displayed a time-dependent depletion of mitochondrial protein thiols, concomitant with an increase in mitochondrial protein carbonyls, while 14CoS/14CoS cells were resistant to such changes. All of the effects produced by TBHP were prevented by desferoxamine.</description><identifier>ISSN: 0893-228X</identifier><identifier>EISSN: 1520-5010</identifier><identifier>DOI: 10.1021/tx00039a013</identifier><identifier>PMID: 8075367</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Animals ; Biological and medical sciences ; Calcium - metabolism ; Cell Death - drug effects ; Cell Line ; Cell Membrane - metabolism ; Cell Nucleus - drug effects ; Cell Nucleus - metabolism ; Chemical and Drug Induced Liver Injury - physiopathology ; Chemical and industrial products toxicology. Toxic occupational diseases ; DNA - chemistry ; Glutathione - metabolism ; Iron - toxicity ; Lipid Peroxidation - drug effects ; Medical sciences ; Mice ; Microscopy, Fluorescence ; Mitochondria, Liver - drug effects ; Oxidation-Reduction ; Peroxides - toxicity ; Reactive Oxygen Species - toxicity ; Spectrometry, Fluorescence ; Sulfhydryl Compounds - pharmacology ; tert-Butylhydroperoxide ; Toxicology ; Various organic compounds</subject><ispartof>Chemical research in toxicology, 1994-05, Vol.7 (3), p.358-366</ispartof><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a383t-8fabdbd0861b36bd94efa0d4185bcf6a2be3365c705654feccf5bbf87dcc36f3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/tx00039a013$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/tx00039a013$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,27055,27915,27916,56757,56807</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3315669$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8075367$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shertzer, Howard G</creatorcontrib><creatorcontrib>Bannenberg, Gerard L</creatorcontrib><creatorcontrib>Zhu, Huan</creatorcontrib><creatorcontrib>Liu, Rui-Ming</creatorcontrib><creatorcontrib>Moldeus, Peter</creatorcontrib><title>The Role of Thiols in Mitochondrial Susceptibility to Iron and tert-Butyl Hydroperoxide-Mediated Toxicity in Cultured Mouse Hepatocytes</title><title>Chemical research in toxicology</title><addtitle>Chem. Res. Toxicol</addtitle><description>Cultured hepatocytes derived from the newborn mutant c14CoS/c14CoS mouse (14CoS/14CoS cells) have 3-fold higher levels of reduced glutathione (GSH) and greater resistance to menadione toxicity than hepatocytes derived from the wild-type cch/cch mouse (ch/ch cells). Therefore, we used these cell lines to examine mechanisms of oxidative stress produced by iron and tert-butyl hydroperoxide (TBHP). Both cell types were resistant to 25 microM Fe2+ toxicity in the absence of added TBHP. However, in the presence of Fe2+, striking differences in susceptibility to TBHP toxicity between the cell types were observed. With 25 microM Fe2+, ch/ch cells showed TBHP concentration-dependent toxicity, with total lethality at 500 microM; in contrast, 14CoS/14CoS cells were completely resistant to the lethal effects of this concentration of TBHP. Concentration-dependent TBHP-mediated increases in cytosolic Ca2+, pH, and GSSG/GSH ratios, and decreases in GSH levels, were evident in ch/ch cells. 14CoS/14CoS cells exhibited concentration-dependent TBHP-mediated changes in GSH and GSSG/GSH ratios, but cytosolic Ca2+ and pH remained at control levels. Mitochondrial GSH pools were also diminished by TBHP, although there was no selective depletion; mitochondrial GSH remained at about 14% of total cellular GSH. Both cell types exhibited the same time-dependent decrease in plasma membrane protein thiols and a time-dependent increase in plasma membrane protein carbonyls. However, only ch/ch cells displayed a time-dependent depletion of mitochondrial protein thiols, concomitant with an increase in mitochondrial protein carbonyls, while 14CoS/14CoS cells were resistant to such changes. All of the effects produced by TBHP were prevented by desferoxamine.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Calcium - metabolism</subject><subject>Cell Death - drug effects</subject><subject>Cell Line</subject><subject>Cell Membrane - metabolism</subject><subject>Cell Nucleus - drug effects</subject><subject>Cell Nucleus - metabolism</subject><subject>Chemical and Drug Induced Liver Injury - physiopathology</subject><subject>Chemical and industrial products toxicology. Toxic occupational diseases</subject><subject>DNA - chemistry</subject><subject>Glutathione - metabolism</subject><subject>Iron - toxicity</subject><subject>Lipid Peroxidation - drug effects</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Microscopy, Fluorescence</subject><subject>Mitochondria, Liver - drug effects</subject><subject>Oxidation-Reduction</subject><subject>Peroxides - toxicity</subject><subject>Reactive Oxygen Species - toxicity</subject><subject>Spectrometry, Fluorescence</subject><subject>Sulfhydryl Compounds - pharmacology</subject><subject>tert-Butylhydroperoxide</subject><subject>Toxicology</subject><subject>Various organic compounds</subject><issn>0893-228X</issn><issn>1520-5010</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><recordid>eNptkE-LFDEQxYMo67h68izkIHiQ1qQzSfcc3dF1FnZwcRrcW8ifCpO1t9MkaZj-BH5ts8wwePBUVL1fvSoeQm8p-URJTT_nAyGErRSh7BlaUF6TihNKnqMFaVesquv2_iV6ldIDIbQsNBfooiUNZ6JZoD_dHvDP0AMODnd7H_qE_YC3PgezD4ONXvV4NyUDY_ba9z7POAd8E8OA1WBxhpirqynPPd7MNoYRYjh4C9UWrFcZLO5Kb57Wiu166vMUy3AbpgR4A6Mqd-YM6TV64VSf4M2pXqLu-lu33lS3P77frL_cVoq1LFetU9pqS1pBNRParpbgFLFL2nJtnFC1BsYENw3hgi8dGOO41q5trDFMOHaJPh5tTQwpRXByjP5RxVlSIp_ClP-EWeh3R3qc9CPYM3tKr-jvT7pKRvUuqsH4dMYYo1yIVcGqI-ZThsNZVvG3LCYNl93dTt5__bXkzd213BX-w5FXJsmHMMWhJPLfB_8CtP-bxw</recordid><startdate>19940501</startdate><enddate>19940501</enddate><creator>Shertzer, Howard G</creator><creator>Bannenberg, Gerard L</creator><creator>Zhu, Huan</creator><creator>Liu, Rui-Ming</creator><creator>Moldeus, Peter</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19940501</creationdate><title>The Role of Thiols in Mitochondrial Susceptibility to Iron and tert-Butyl Hydroperoxide-Mediated Toxicity in Cultured Mouse Hepatocytes</title><author>Shertzer, Howard G ; Bannenberg, Gerard L ; Zhu, Huan ; Liu, Rui-Ming ; Moldeus, Peter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a383t-8fabdbd0861b36bd94efa0d4185bcf6a2be3365c705654feccf5bbf87dcc36f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Calcium - metabolism</topic><topic>Cell Death - drug effects</topic><topic>Cell Line</topic><topic>Cell Membrane - metabolism</topic><topic>Cell Nucleus - drug effects</topic><topic>Cell Nucleus - metabolism</topic><topic>Chemical and Drug Induced Liver Injury - physiopathology</topic><topic>Chemical and industrial products toxicology. Toxic occupational diseases</topic><topic>DNA - chemistry</topic><topic>Glutathione - metabolism</topic><topic>Iron - toxicity</topic><topic>Lipid Peroxidation - drug effects</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Microscopy, Fluorescence</topic><topic>Mitochondria, Liver - drug effects</topic><topic>Oxidation-Reduction</topic><topic>Peroxides - toxicity</topic><topic>Reactive Oxygen Species - toxicity</topic><topic>Spectrometry, Fluorescence</topic><topic>Sulfhydryl Compounds - pharmacology</topic><topic>tert-Butylhydroperoxide</topic><topic>Toxicology</topic><topic>Various organic compounds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shertzer, Howard G</creatorcontrib><creatorcontrib>Bannenberg, Gerard L</creatorcontrib><creatorcontrib>Zhu, Huan</creatorcontrib><creatorcontrib>Liu, Rui-Ming</creatorcontrib><creatorcontrib>Moldeus, Peter</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Chemical research in toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shertzer, Howard G</au><au>Bannenberg, Gerard L</au><au>Zhu, Huan</au><au>Liu, Rui-Ming</au><au>Moldeus, Peter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Role of Thiols in Mitochondrial Susceptibility to Iron and tert-Butyl Hydroperoxide-Mediated Toxicity in Cultured Mouse Hepatocytes</atitle><jtitle>Chemical research in toxicology</jtitle><addtitle>Chem. Res. Toxicol</addtitle><date>1994-05-01</date><risdate>1994</risdate><volume>7</volume><issue>3</issue><spage>358</spage><epage>366</epage><pages>358-366</pages><issn>0893-228X</issn><eissn>1520-5010</eissn><abstract>Cultured hepatocytes derived from the newborn mutant c14CoS/c14CoS mouse (14CoS/14CoS cells) have 3-fold higher levels of reduced glutathione (GSH) and greater resistance to menadione toxicity than hepatocytes derived from the wild-type cch/cch mouse (ch/ch cells). Therefore, we used these cell lines to examine mechanisms of oxidative stress produced by iron and tert-butyl hydroperoxide (TBHP). Both cell types were resistant to 25 microM Fe2+ toxicity in the absence of added TBHP. However, in the presence of Fe2+, striking differences in susceptibility to TBHP toxicity between the cell types were observed. With 25 microM Fe2+, ch/ch cells showed TBHP concentration-dependent toxicity, with total lethality at 500 microM; in contrast, 14CoS/14CoS cells were completely resistant to the lethal effects of this concentration of TBHP. Concentration-dependent TBHP-mediated increases in cytosolic Ca2+, pH, and GSSG/GSH ratios, and decreases in GSH levels, were evident in ch/ch cells. 14CoS/14CoS cells exhibited concentration-dependent TBHP-mediated changes in GSH and GSSG/GSH ratios, but cytosolic Ca2+ and pH remained at control levels. Mitochondrial GSH pools were also diminished by TBHP, although there was no selective depletion; mitochondrial GSH remained at about 14% of total cellular GSH. Both cell types exhibited the same time-dependent decrease in plasma membrane protein thiols and a time-dependent increase in plasma membrane protein carbonyls. However, only ch/ch cells displayed a time-dependent depletion of mitochondrial protein thiols, concomitant with an increase in mitochondrial protein carbonyls, while 14CoS/14CoS cells were resistant to such changes. All of the effects produced by TBHP were prevented by desferoxamine.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>8075367</pmid><doi>10.1021/tx00039a013</doi><tpages>9</tpages></addata></record> |
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ispartof | Chemical research in toxicology, 1994-05, Vol.7 (3), p.358-366 |
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source | ACS CRKN Legacy Archives |
subjects | Animals Biological and medical sciences Calcium - metabolism Cell Death - drug effects Cell Line Cell Membrane - metabolism Cell Nucleus - drug effects Cell Nucleus - metabolism Chemical and Drug Induced Liver Injury - physiopathology Chemical and industrial products toxicology. Toxic occupational diseases DNA - chemistry Glutathione - metabolism Iron - toxicity Lipid Peroxidation - drug effects Medical sciences Mice Microscopy, Fluorescence Mitochondria, Liver - drug effects Oxidation-Reduction Peroxides - toxicity Reactive Oxygen Species - toxicity Spectrometry, Fluorescence Sulfhydryl Compounds - pharmacology tert-Butylhydroperoxide Toxicology Various organic compounds |
title | The Role of Thiols in Mitochondrial Susceptibility to Iron and tert-Butyl Hydroperoxide-Mediated Toxicity in Cultured Mouse Hepatocytes |
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