Gene profile of replicative senescence is different from progeria or elderly donor

被引:39
作者
Park, WY
Hwang, CI
Kang, MJ
Seo, JY
Chung, JH
Kim, YS
Lee, JH
Kim, H
Kim, KA
Yoo, HJ
Seo, JS
机构
[1] Seoul Natl Univ, Dept Biochem & Mol Biol, Coll Med, Chongno Gu, Seoul 110799, South Korea
[2] Seoul Natl Univ, Dept Dermatol, Coll Med, Chongno Gu, Seoul 110799, South Korea
[3] Seoul Natl Univ, Dept Internal Med, Coll Med, Chongno Gu, Seoul 110799, South Korea
[4] Seoul Natl Univ, Grad Sch Publ Hlth, Dept Biostat, Seoul, South Korea
关键词
cDNA microarray; aging; HDF; progeria; replicative senescence;
D O I
10.1006/bbrc.2001.4632
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In vitro cellular senescence of human diploid fibroblast has been a good model for aging research, which shows similar phenotypes to in vivo aging. Gene expression profiling would provide an insight to understand the mechanism of senescence. Using cDNA microarray containing 384 known genes, we compared the expression profiles of three different types of aging models: replicative senescence, fibroblasts from progeria or from elderly donor. Although all of them showed senescence phenotypes, distinct sets of genes were altered in each group. Pairwise plots or cluster analysis of activation fold of gene expression revealed closer relationships between fibroblasts from progeria or from old individual, but not between replicative senescence fibroblasts and either models. Differential expression pattern of several genes were confirmed by RT-PCR, We suggest that the replicative senescence model might behave differently to other types of aging models due to the distinct gene expression. (C) 2001 Academic Press.
引用
收藏
页码:934 / 939
页数:6
相关论文
共 24 条
[1]  
BIERMAN EL, 1978, IN VITRO CELL DEV B, V14, P951
[2]  
Brown W T, 1990, Annu Rev Gerontol Geriatr, V10, P23
[3]   INVITRO SENESCENCE OF SYRIAN-HAMSTER MESENCHYMAL CELLS OF FETAL TO AGED ADULT ORIGIN - INVERSE RELATIONSHIP BETWEEN INVIVO DONOR AGE AND INVITRO PROLIFERATIVE CAPACITY [J].
BRUCE, SA ;
DEAMOND, SF ;
TSO, POP .
MECHANISMS OF AGEING AND DEVELOPMENT, 1986, 34 (02) :151-173
[4]   A BIOMARKER THAT IDENTIFIES SENESCENT HUMAN-CELLS IN CULTURE AND IN AGING SKIN IN-VIVO [J].
DIMRI, GP ;
LEE, XH ;
BASILE, G ;
ACOSTA, M ;
SCOTT, C ;
ROSKELLEY, C ;
MEDRANO, EE ;
LINSKENS, M ;
RUBELJ, I ;
PEREIRASMITH, O ;
PEACOCKE, M ;
CAMPISI, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (20) :9363-9367
[5]   Amelioration of age-related deficits in the stimulation of synapsin phosphorylation [J].
Eckles, KE ;
Dudek, EM ;
Bickford, PC ;
Browning, MD .
NEUROBIOLOGY OF AGING, 1997, 18 (02) :213-217
[6]   Cluster analysis and display of genome-wide expression patterns [J].
Eisen, MB ;
Spellman, PT ;
Brown, PO ;
Botstein, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14863-14868
[7]   TELOMERES SHORTEN DURING AGING OF HUMAN FIBROBLASTS [J].
HARLEY, CB ;
FUTCHER, AB ;
GREIDER, CW .
NATURE, 1990, 345 (6274) :458-460
[8]   LIMITED IN VITRO LIFETIME OF HUMAN DIPLOID CELL STRAINS [J].
HAYFLICK, L .
EXPERIMENTAL CELL RESEARCH, 1965, 37 (03) :614-&
[9]   The CREC family, a novel family of multiple EF-hand, low-affinity Ca2+-binding proteins localised to the secretory pathway of mammalian cells [J].
Honoré, B ;
Vorum, H .
FEBS LETTERS, 2000, 466 (01) :11-18
[10]   Specific loss of protein kinase activities in senescent erythrocytes [J].
Jindal, HK ;
Ai, ZW ;
Gascard, P ;
Horton, C ;
Cohen, CM .
BLOOD, 1996, 88 (04) :1479-1487