Microarray analysis reveals similarity between CD8+CD28- T cells from young and elderly persons, but not of CD8+CD28+ T cells

被引:36
|
作者
Lazuardi, Lutfan [1 ]
Herndler-Brandstetter, Dietmar [1 ]
Brunner, Stefan [1 ]
Laschober, Gerhard T. [1 ]
Lepperdinger, Guenter [1 ]
Grubeck-Loebenstein, Beatrix [1 ]
机构
[1] Austrian Acad Sci, Inst Biomed Aging Res, A-6020 Innsbruck, Austria
基金
奥地利科学基金会;
关键词
Aging; Humans; CD8(+) T cell; Gene expression; SOLUBLE INTERLEUKIN-6 RECEPTOR; EXPRESSION; ACTIVATION; MEMORY; DIFFERENTIATION; CENTENARIANS; LYMPHOCYTES; PHENOTYPE; EXPANSION; HUMANS;
D O I
10.1007/s10522-008-9167-1
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
We isolated highly purified CD8(+)CD28(+) and CD8(+)CD28(-) T cell populations from healthy young and elderly persons for gene expression profiling using Affymetrix oligonucleotide microarrays. We demonstrate that the gene expression profile of CD8(+)CD28(-) T cells is very similar in young and elderly persons. In contrast, CD8(+)CD28(+) in elderly differ from CD8(+)CD28(+) in young persons. Hierarchical clustering revealed that CD8(+)CD28(+) in elderly are located between CD8(+)CD28(+) in young and CD8(+)CD28(-) (young and old) T cells regarding their differentiation state. Our study demonstrates a dichotomy of gene expression levels between CD8(+)CD28(+) T cells in young and elderly persons but a similarity between CD8(+)CD28(-) T cells in young and elderly persons. As CD8(+)CD28(+) T cells from elderly and young persons are distinct due to a different composition of the population, these results suggest that the gene expression profile does not depend on chronological age but depends on the differentiation state of the individual cell types.
引用
收藏
页码:191 / 202
页数:12
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