Enhanced expression of mitochondrial genes in senescent endothelial cells and fibroblasts

被引:18
作者
Kumazaki, T
Sakano, T
Yoshida, T
Hamada, K
Sumida, H
Teranishi, Y
Nishiyama, M
Mitsui, Y
机构
[1] Hiroshima Univ, Dept Biochem & Biophys, Res Inst Radiat Biol & Med, Minami Ku, Hiroshima 734, Japan
[2] Natl Inst Biosci & Human Technol, Agcy Ind Sci & Technol, Tsukuba, Ibaraki 305, Japan
[3] Hiroshima Univ, Dept Mol Pathol, Res Inst Radiat Biol & Med, Minami Ku, Hiroshima 734, Japan
[4] Sanyo Womens Coll, Div Anat & Physiol, Hatsukaichi 738, Japan
[5] Hiroshima Univ, Sch Med, Dept Physiol, Hiroshima 734, Japan
关键词
cellular senescence; endothelial cell; fibroblast; mitochondria; gene expression;
D O I
10.1016/S0047-6374(97)00159-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
It has been suggested that some mitochondrial genes are important in cellular senescence. In order to identify the mitochondrial genes that are involved in cellular senescence, we have constructed a cDNA library from senescent human vascular endothelial cells and isolated 86 senescence-specific cDNA clones by differential screening. Among the clones, we identified four distinct mitochondrial genes including NADH dehydrogenase subunit 2 (ND2), ND3, ATPase 6 and 16S ribosomal RNA. We then compared the levels of expression of these genes in young and senescent cells by using two endothelial and two fibroblast cell strains. Northern blot and slot blot hybridization confirmed that the expression levels of ND3, ATPase 6 and 16S rRNA were elevated in senescent cells of all four strains. The expression level of ND2 was also elevated during cellular senescence in three of the four strains. Because mitochondria an actively involved in oxidative phosphorylation and respiratory functions, the altered expression levels of these genes may participate in aging processes. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:91 / 99
页数:9
相关论文
共 37 条
[1]  
Brown MD, 1997, AM J HUM GENET, V60, P381
[2]   RAPID EVOLUTION OF ANIMAL MITOCHONDRIAL-DNA [J].
BROWN, WM ;
GEORGE, M ;
WILSON, AC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (04) :1967-1971
[3]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[4]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[5]   RETRACTED: Mutations in mitochondrial cytochrome c oxidase genes segregate with late-onset Alzheimer disease (Retracted Article) [J].
Davis, RE ;
Miller, S ;
Herrnstadt, C ;
Ghosh, SS ;
Fahy, E ;
Shinobu, LA ;
Galasko, D ;
Thal, LJ ;
Beal, MF ;
Howell, N ;
Parker, WD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (09) :4526-4531
[6]   DIFFERENTIAL GENE-EXPRESSION BETWEEN YOUNG AND SENESCENT, QUIESCENT WI-38 CELLS [J].
DOGGETT, DL ;
ROTENBERG, MO ;
PIGNOLO, RJ ;
PHILLIPS, PD ;
CRISTOFALO, VJ .
MECHANISMS OF AGEING AND DEVELOPMENT, 1992, 65 (2-3) :239-255
[7]   REDUCED SYNTHESIS OF MESSENGER TRANSFER-RNA IN ISOLATED-MITOCHONDRIA OF SENESCENT RAT-BRAIN [J].
FERNANDEZSILVA, P ;
PETRUZZELLA, V ;
FRACASSO, F ;
GADALETA, MN ;
CANTATORE, P .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 176 (02) :645-653
[8]   ENHANCED EXPRESSION OF CYCLIN D-1 IN SENESCENT HUMAN FIBROBLASTS [J].
FUKAMI, J ;
ANNO, K ;
UEDA, K ;
TAKAHASHI, T ;
IDE, T .
MECHANISMS OF AGEING AND DEVELOPMENT, 1995, 81 (2-3) :139-157
[9]   ENERGY-METABOLISM IN CULTURED HUMAN-FIBROBLASTS DURING AGING INVITRO [J].
GOLDSTEIN, S ;
BALLANTYNE, SR ;
ROBSON, AL ;
MOERMAN, EJ .
JOURNAL OF CELLULAR PHYSIOLOGY, 1982, 112 (03) :419-424
[10]   Age-related extensive fragmentation of mitochondrial DNA into minicircles [J].
Hayakawa, M ;
Katsumata, K ;
Yoneda, M ;
Tanaka, M ;
Sugiyama, S ;
Ozawa, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 226 (02) :369-377