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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
Main Authors: Shertzer, Howard G, Bannenberg, Gerard L, Zhu, Huan, Liu, Rui-Ming, Moldeus, Peter
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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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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. 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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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identifier ISSN: 0893-228X
ispartof Chemical research in toxicology, 1994-05, Vol.7 (3), p.358-366
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1520-5010
language eng
recordid cdi_crossref_primary_10_1021_tx00039a013
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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