Development and Age-associated Differences in Electron Transport Potential and Consequences for Oxidant Generation

We determined the activities of NADH dehydrogenase (ND), succinate dehydrogenase, and cytochromec oxidase (COX) in 29 skin fibroblast lines established from donors ranging in age from 12 gestational weeks to 94 years. The results of this study demonstrate that all three of the enzyme activities exam...

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Veröffentlicht in:The Journal of biological chemistry 1997-10, Vol.272 (40), p.24805-24812
Hauptverfasser: Allen, Robert G., Keogh, Bart P., Tresini, Maria, Gerhard, Glenn S., Volker, Craig, Pignolo, Robert J., Horton, Joseph, Cristofalo, Vincent J.
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container_end_page 24812
container_issue 40
container_start_page 24805
container_title The Journal of biological chemistry
container_volume 272
creator Allen, Robert G.
Keogh, Bart P.
Tresini, Maria
Gerhard, Glenn S.
Volker, Craig
Pignolo, Robert J.
Horton, Joseph
Cristofalo, Vincent J.
description We determined the activities of NADH dehydrogenase (ND), succinate dehydrogenase, and cytochromec oxidase (COX) in 29 skin fibroblast lines established from donors ranging in age from 12 gestational weeks to 94 years. The results of this study demonstrate that all three of the enzyme activities examined are greater in adult-derived fibroblasts than in the fetal cell lines. The ratio of enzyme activities that control electron entry into and exit from the electron transport chain varied directly with lucigenin-detected chemiluminescence (an indicator of⋅O2− generation) and inversely with H2O2 generation. These results indicate a clear difference in the predominant oxidant species generated during fetal and adult stages of life. We also examined the mRNA abundances of different components of the electron transport chain complexes. We observed higher abundances of mitochondrial encoded mRNAs (COX 1 and ND 4) in cell lines established from adults than in fetal cells. No differences in the mRNA abundances of the nuclear encoded sequences (COX 4 and ND 51) were observed in fetal and postnatal-derived lines. Succinate dehydrogenase mRNA abundance was greater in cell lines established from postnatal donors than in fetal cell lines. No significant differences between cell lines established from young and old adults were detected in any of the parameters examined.
doi_str_mv 10.1074/jbc.272.40.24805
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The results of this study demonstrate that all three of the enzyme activities examined are greater in adult-derived fibroblasts than in the fetal cell lines. The ratio of enzyme activities that control electron entry into and exit from the electron transport chain varied directly with lucigenin-detected chemiluminescence (an indicator of⋅O2− generation) and inversely with H2O2 generation. These results indicate a clear difference in the predominant oxidant species generated during fetal and adult stages of life. We also examined the mRNA abundances of different components of the electron transport chain complexes. We observed higher abundances of mitochondrial encoded mRNAs (COX 1 and ND 4) in cell lines established from adults than in fetal cells. No differences in the mRNA abundances of the nuclear encoded sequences (COX 4 and ND 51) were observed in fetal and postnatal-derived lines. Succinate dehydrogenase mRNA abundance was greater in cell lines established from postnatal donors than in fetal cell lines. 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Succinate dehydrogenase mRNA abundance was greater in cell lines established from postnatal donors than in fetal cell lines. 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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Adult
Aged
Aged, 80 and over
Aging - metabolism
Cell Line
Child
Electron Transport
Electron Transport Complex IV - metabolism
Embryonic and Fetal Development
Fetus
Fibroblasts - enzymology
Humans
Infant, Newborn
Macromolecular Substances
NADH Dehydrogenase - metabolism
RNA, Messenger - metabolism
Skin - embryology
Skin - enzymology
Skin - growth & development
Succinate Dehydrogenase - metabolism
title Development and Age-associated Differences in Electron Transport Potential and Consequences for Oxidant Generation
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