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PMID: 10362024 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Differences in electron transport potential, antioxidant defenses, and oxidant generation in young and senescent fetal lung fibroblasts (WI-38).

Journal of cellular physiology ·Vol. 180 ·No. 1 ·1999-07-00 ·Pages 114-22

Allen RG, Tresini M, Keogh BP, Doggett DL, Cristofalo VJ

Abstract

The activities and mRNA abundances of enzymes that regulate the rate of electron flow through the electron transport chain (ETC), including NADH dehydrogenase, succinate dehydrogenase, and cytochrome c oxidase, were examined in young and senescent fetal lung fibroblasts (WI-38). We also determined the activities and mRNA abundances of antioxidant defenses including superoxide dismutase, catalase, and glutathione peroxidase. We confirmed our previous report of a senescence-related increase in the abundance of ND4, a mitochondrially encoded subunit of NADH dehydrogenase. The activities of cytochrome c oxidase and NADH dehydrogenase were also elevated in senescent cultures. No differences were observed in the mRNA abundances of COX-1, a mitochondrially encoded subunit of cytochrome c oxidase or of nuclearly encoded subunits of various electron transport components (SD, COX-4, and ND 51). Lucigenin-detected chemiluminescence and H2O2 generation were both elevated in senescent cells. Catalase activity was also elevated in senescent fibroblasts. However, no differences in catalase mRNA abundance were observed. A small decrease in GSH peroxidase (GPx) mRNA abundance was observed in senescent cells. No other changes in the activities or mRNA abundances of any of the antioxidant defenses were observed in early and late passage cultures. The relationships between oxidant generation, mitochondrial enzyme activities, and antioxidant defense observed during proliferative senescence are dissimilar to those detected between fetal and postnatal fibroblasts as well as those found between fibroblast lines obtained from young and old individuals. The relevance of the differences between these models is discussed.

MeSH Terms
Acridines Antioxidants/metabolism Catalase/genetics,metabolism Cells, Cultured Cellular Senescence/physiology Electron Transport/physiology Electron Transport Complex IV/genetics,metabolism Fetus/cytology,enzymology Fibroblasts/cytology,enzymology Gene Expression Regulation, Enzymologic Glutathione/metabolism Glutathione Peroxidase/genetics,metabolism Humans Hydrogen Peroxide/metabolism Luminescent Measurements Lung/cytology,embryology,metabolism Mitochondria/enzymology NADH Dehydrogenase/genetics,metabolism RNA, Messenger/analysis Succinate Dehydrogenase/genetics,metabolism Superoxide Dismutase/genetics,metabolism Superoxide Dismutase-1
Chemicals
Acridines Antioxidants NADH dehydrogenase subunit 4 RNA, Messenger SOD1 protein, human 10,10'-dimethyl-9,9'-biacridinium Hydrogen Peroxide Catalase Glutathione Peroxidase Superoxide Dismutase Superoxide Dismutase-1 Succinate Dehydrogenase NADH Dehydrogenase Electron Transport Complex IV Glutathione
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Allen R G
Center for Gerontological Research, Allegheny University, Philadelphia, Pennsylvania, USA.
Tresini M
Keogh B P
Doggett D L
Cristofalo V J
Article Info
Journal
Journal of cellular physiology
Abbr.
J Cell Physiol
ISSN
0021-9541
Published
1999-07-00
Pages
114-22
Language
English
Region
United States
NLM ID
0050222
Subset
IM
Grants
NIA NIH HHS · AG00131 · United States
NIA NIH HHS · AG00378 · United States
NIA NIH HHS · AG00523 · United States
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