Cited by 43T-cell and B-cell ImmunologyGenetics, Aging, and Longevity in Model OrganismsTelomeres, Telomerase, and Senescence

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

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Lazuardi, Lutfan, Herndler-Brandstetter, Dietmar, Brunner, Stefan, Laschober, Gerhard T., Lepperdinger, Günter, Grubeck-Loebenstein, Beatrix·2009·Biogerontology

Abstract

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.

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Crossref · 10.1007/s10522-008-9167-1

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  • Separate analysis of CD28+ and CD28− CD8+ T cells in young and old individuals was consistent with old CD28+CD8+ T cells being more differentiated, as also suggested by epigenetic studies.

    “A separate analysis of CD28+ and CD28− CD8+ T cells in young and old individuals were consistent with the model that old CD28+CD8+ T cells were more differentiated (Lazuardi et al., 2009) as also suggested by the epigenetic studies of CD8+ T cell subsets (Moskowitz et al., 2017).”

    From Successful and Maladaptive T Cell Aging (2017) · cites this paper as Lazuardi et al., 2009

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References 31 · Cited by 43

Authors
Lazuardi, L., Herndler-Brandstetter, D., Brunner, S., Laschober, G. T., Lepperdinger, G., & Grubeck-Loebenstein, B.
Affiliations
Austrian Academy of Sciences (AT)
Venue
Biogerontology
Published
2008-08-27
Volume
10
Issue
2
Pages
191-202
ISSN
  • 1389-5729 (ISSN-L)
  • 1573-6768
OpenAlex
W2082872592
Cited by
43
References
31
Citations by year
2026: 1 · 2025: 1 · 2023: 1 · 2022: 3 · 2021: 1 · 2019: 2 · 2018: 1 · 2017: 3 · 2016: 1 · 2015: 3 · 2014: 2 · 2013: 2 · 2012: 5
FWCI
2.36
Type
journal article
Language
en
Open access
Locations
  • Biogerontology (publishedVersion)
  • PubMed (publishedVersion)
  • Oesterreichisches Musiklexikon online (Institut für kunst- und musikhistorische Forschungen der Österreichischen Akademie der Wissenschaften) (submittedVersion, other-oa)
  • Austrian Biographical Dictionary (Austrian Academy of Sciences) (submittedVersion, other-oa)
Funders
Austrian Science Fund
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
  • Health Sciences › Medicine › Physiology › Telomeres, Telomerase, and Senescence
Keywords
CD8+CD28- T cells, T cell gene expression, aging, age-related gene expression, T cell differentiation, gene expression profiling
MeSH terms
Adult, Age Factors, Aged, Aged, 80 and over, Aging, Cell Differentiation, Female, Humans, Immunologic Memory, Male, Reproducibility of Results, Cluster Analysis, T-Lymphocyte Subsets, CD28 Antigens, CD8-Positive T-Lymphocytes, Reverse Transcriptase Polymerase Chain Reaction, Oligonucleotide Array Sequence Analysis, Gene Expression Profiling

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