Abstract
Human skin contains various populations of memory T cells in permanent residence and in transit. Arguably, the best characterized of the skin subsets are the CD8(+) permanently resident memory T cells (TRM) expressing the integrin subunit, CD103. In order to investigate the remaining skin T cells, we isolated skin-tropic (CLA(+)) helper T cells, regulatory T cells, and CD8(+) CD103(-) T cells from skin and blood for RNA microarray analysis to compare the transcriptional profiles of these groups. We found that despite their common tropism, the T cells isolated from skin were transcriptionally distinct from blood-derived CLA(+) T cells. A shared pool of genes contributed to the skin/blood discrepancy, with substantial overlap in differentially expressed genes between each T cell subset. Gene set enrichment analysis further showed that the differential gene profiles of each human skin T cell subset were significantly enriched for previously identified TRM core signature genes. Our results support the hypothesis that human skin may contain additional TRM or TRM-like populations.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adolescent
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Adult
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Aged
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Antigens, CD / genetics
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Antigens, CD / immunology
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CD8 Antigens / genetics
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CD8 Antigens / immunology
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CD8-Positive T-Lymphocytes / cytology
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CD8-Positive T-Lymphocytes / immunology
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CD8-Positive T-Lymphocytes / metabolism*
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Female
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Gene Expression Profiling
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Gene Expression Regulation
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Humans
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Immunophenotyping
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Integrin alpha Chains / genetics
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Integrin alpha Chains / immunology
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Leukocytes, Mononuclear / cytology
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Leukocytes, Mononuclear / immunology
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Leukocytes, Mononuclear / metabolism
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Middle Aged
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Molecular Sequence Annotation
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Oligonucleotide Array Sequence Analysis
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Organ Specificity
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Skin / cytology
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Skin / immunology
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Skin / metabolism*
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T-Lymphocytes, Helper-Inducer / cytology
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T-Lymphocytes, Helper-Inducer / immunology
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T-Lymphocytes, Helper-Inducer / metabolism*
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T-Lymphocytes, Regulatory / cytology
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T-Lymphocytes, Regulatory / immunology
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T-Lymphocytes, Regulatory / metabolism*
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Transcription, Genetic*
Substances
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Antigens, CD
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CD8 Antigens
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Integrin alpha Chains
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alpha E integrins
Grants and funding
The work was supported by grants from the Australian National Health and Medical Research Council to FRC. JL is a recipient of the Elizabeth and Vernon Puzey Scholarship. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.