Sites and Mechanisms of Low-Level Oxidative Stress in Cultured Cells
Oxidative stress is involved in a multitude of pathological conditions. In the present study, we investigated the cellular targets and the mechanisms of low-level oxidative stress in a Chinese Hamster Ovary cell culture. Oxidative stress was induced either by continuous enzymatic production of super...
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Veröffentlicht in: | Biochemical and biophysical research communications 1995-01, Vol.206 (1), p.421-428 |
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description | Oxidative stress is involved in a multitude of pathological conditions. In the present study, we investigated the cellular targets and the mechanisms of low-level oxidative stress in a Chinese Hamster Ovary cell culture. Oxidative stress was induced either by continuous enzymatic production of superoxide or by bolus addition of hydrogen peroxide (H2O2). Low-level oxidative stress irreversibly impaired the reproductive capacity of the cells in the absence of damage to membrane integrity or energy metabolism. Cells were protected by catalase but not by superoxide dismutase, indicating that H2O2 not superoxide, was the causative agent of cell damage. Nitroxide spin labels decreased hydroxyl radical (•OH) formation and protected cells from the oxidative stress. The differing membrane permeabilities of these spin labels suggest that the damage is localized on the cell surface. Oxidative stress to DNA and RNA was not significant, as shown by levels of guanine hydroxylation products. A mechanism is proposed whereby low-level oxidative stress acts at the cell surface to cause impairment of cell reproduction. |
doi_str_mv | 10.1006/bbrc.1995.1058 |
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In the present study, we investigated the cellular targets and the mechanisms of low-level oxidative stress in a Chinese Hamster Ovary cell culture. Oxidative stress was induced either by continuous enzymatic production of superoxide or by bolus addition of hydrogen peroxide (H2O2). Low-level oxidative stress irreversibly impaired the reproductive capacity of the cells in the absence of damage to membrane integrity or energy metabolism. Cells were protected by catalase but not by superoxide dismutase, indicating that H2O2 not superoxide, was the causative agent of cell damage. Nitroxide spin labels decreased hydroxyl radical (•OH) formation and protected cells from the oxidative stress. The differing membrane permeabilities of these spin labels suggest that the damage is localized on the cell surface. Oxidative stress to DNA and RNA was not significant, as shown by levels of guanine hydroxylation products. A mechanism is proposed whereby low-level oxidative stress acts at the cell surface to cause impairment of cell reproduction.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1006/bbrc.1995.1058</identifier><identifier>PMID: 7818547</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Catalase - pharmacology ; Cell Survival - drug effects ; CHO Cells ; Cricetinae ; Cyclic N-Oxides ; Dose-Response Relationship, Drug ; Electron Spin Resonance Spectroscopy ; Hydrogen Peroxide - pharmacology ; Hydroxyl Radical - metabolism ; L-Lactate Dehydrogenase ; Oxidative Stress ; Spin Labels ; Superoxide Dismutase - pharmacology ; Superoxides - metabolism</subject><ispartof>Biochemical and biophysical research communications, 1995-01, Vol.206 (1), p.421-428</ispartof><rights>1995 Academic Press</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c339t-62e314321f09b3fc90652dba717f8a31c5cd801863b7af767d6017c0fdd143443</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1006/bbrc.1995.1058$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7818547$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gelvan, D.</creatorcontrib><creatorcontrib>Moreno, V.</creatorcontrib><creatorcontrib>Clopton, D.A.</creatorcontrib><creatorcontrib>Chen, Q.</creatorcontrib><creatorcontrib>Saltman, P.</creatorcontrib><title>Sites and Mechanisms of Low-Level Oxidative Stress in Cultured Cells</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>Oxidative stress is involved in a multitude of pathological conditions. In the present study, we investigated the cellular targets and the mechanisms of low-level oxidative stress in a Chinese Hamster Ovary cell culture. Oxidative stress was induced either by continuous enzymatic production of superoxide or by bolus addition of hydrogen peroxide (H2O2). Low-level oxidative stress irreversibly impaired the reproductive capacity of the cells in the absence of damage to membrane integrity or energy metabolism. Cells were protected by catalase but not by superoxide dismutase, indicating that H2O2 not superoxide, was the causative agent of cell damage. Nitroxide spin labels decreased hydroxyl radical (•OH) formation and protected cells from the oxidative stress. The differing membrane permeabilities of these spin labels suggest that the damage is localized on the cell surface. Oxidative stress to DNA and RNA was not significant, as shown by levels of guanine hydroxylation products. A mechanism is proposed whereby low-level oxidative stress acts at the cell surface to cause impairment of cell reproduction.</description><subject>Animals</subject><subject>Catalase - pharmacology</subject><subject>Cell Survival - drug effects</subject><subject>CHO Cells</subject><subject>Cricetinae</subject><subject>Cyclic N-Oxides</subject><subject>Dose-Response Relationship, Drug</subject><subject>Electron Spin Resonance Spectroscopy</subject><subject>Hydrogen Peroxide - pharmacology</subject><subject>Hydroxyl Radical - metabolism</subject><subject>L-Lactate Dehydrogenase</subject><subject>Oxidative Stress</subject><subject>Spin Labels</subject><subject>Superoxide Dismutase - pharmacology</subject><subject>Superoxides - metabolism</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kLtPwzAQxi0EKqWwsiF5Ykvx5eVkROUpBXUoSGyWY5-FUR5gJwX-exy1YmM6ne77vrv7EXIObAmM5Vd17dQSyjILbVYckDmwkkUxsPSQzFlQRHEJr8fkxPt3xgDSvJyRGS-gyFI-JzcbO6CnstP0CdWb7KxvPe0NrfqvqMItNnT9bbUc7BbpZnDoPbUdXY3NMDrUdIVN40_JkZGNx7N9XZCXu9vn1UNUre8fV9dVpJKkHKI8xgTSJAbDyjoxqmR5FutacuCmkAmoTOmCQZEnNZeG51znDLhiRutgS9NkQS53uR-u_xzRD6K1XoULZIf96AXnEIcNRRAud0Lleu8dGvHhbCvdjwAmJmxiwiYmbGLCFgwX--SxblH_yfecwrzYzTG8t7XohFcWO4XaOlSD0L39L_oXrnV6ew</recordid><startdate>19950105</startdate><enddate>19950105</enddate><creator>Gelvan, D.</creator><creator>Moreno, V.</creator><creator>Clopton, D.A.</creator><creator>Chen, Q.</creator><creator>Saltman, P.</creator><general>Elsevier Inc</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>19950105</creationdate><title>Sites and Mechanisms of Low-Level Oxidative Stress in Cultured Cells</title><author>Gelvan, D. ; Moreno, V. ; Clopton, D.A. ; Chen, Q. ; Saltman, P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c339t-62e314321f09b3fc90652dba717f8a31c5cd801863b7af767d6017c0fdd143443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Animals</topic><topic>Catalase - pharmacology</topic><topic>Cell Survival - drug effects</topic><topic>CHO Cells</topic><topic>Cricetinae</topic><topic>Cyclic N-Oxides</topic><topic>Dose-Response Relationship, Drug</topic><topic>Electron Spin Resonance Spectroscopy</topic><topic>Hydrogen Peroxide - pharmacology</topic><topic>Hydroxyl Radical - metabolism</topic><topic>L-Lactate Dehydrogenase</topic><topic>Oxidative Stress</topic><topic>Spin Labels</topic><topic>Superoxide Dismutase - pharmacology</topic><topic>Superoxides - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gelvan, D.</creatorcontrib><creatorcontrib>Moreno, V.</creatorcontrib><creatorcontrib>Clopton, D.A.</creatorcontrib><creatorcontrib>Chen, Q.</creatorcontrib><creatorcontrib>Saltman, P.</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>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gelvan, D.</au><au>Moreno, V.</au><au>Clopton, D.A.</au><au>Chen, Q.</au><au>Saltman, P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sites and Mechanisms of Low-Level Oxidative Stress in Cultured Cells</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>1995-01-05</date><risdate>1995</risdate><volume>206</volume><issue>1</issue><spage>421</spage><epage>428</epage><pages>421-428</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>Oxidative stress is involved in a multitude of pathological conditions. In the present study, we investigated the cellular targets and the mechanisms of low-level oxidative stress in a Chinese Hamster Ovary cell culture. Oxidative stress was induced either by continuous enzymatic production of superoxide or by bolus addition of hydrogen peroxide (H2O2). Low-level oxidative stress irreversibly impaired the reproductive capacity of the cells in the absence of damage to membrane integrity or energy metabolism. Cells were protected by catalase but not by superoxide dismutase, indicating that H2O2 not superoxide, was the causative agent of cell damage. Nitroxide spin labels decreased hydroxyl radical (•OH) formation and protected cells from the oxidative stress. The differing membrane permeabilities of these spin labels suggest that the damage is localized on the cell surface. Oxidative stress to DNA and RNA was not significant, as shown by levels of guanine hydroxylation products. A mechanism is proposed whereby low-level oxidative stress acts at the cell surface to cause impairment of cell reproduction.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>7818547</pmid><doi>10.1006/bbrc.1995.1058</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Catalase - pharmacology Cell Survival - drug effects CHO Cells Cricetinae Cyclic N-Oxides Dose-Response Relationship, Drug Electron Spin Resonance Spectroscopy Hydrogen Peroxide - pharmacology Hydroxyl Radical - metabolism L-Lactate Dehydrogenase Oxidative Stress Spin Labels Superoxide Dismutase - pharmacology Superoxides - metabolism |
title | Sites and Mechanisms of Low-Level Oxidative Stress in Cultured Cells |
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