Transcriptional Analysis of T Cells Resident in Human Skin

PLoS One. 2016 Jan 29;11(1):e0148351. doi: 10.1371/journal.pone.0148351. eCollection 2016.

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

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Antigens, CD / genetics
  • Antigens, CD / immunology
  • CD8 Antigens / genetics
  • CD8 Antigens / immunology
  • CD8-Positive T-Lymphocytes / cytology
  • CD8-Positive T-Lymphocytes / immunology
  • CD8-Positive T-Lymphocytes / metabolism*
  • Female
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Humans
  • Immunophenotyping
  • Integrin alpha Chains / genetics
  • Integrin alpha Chains / immunology
  • Leukocytes, Mononuclear / cytology
  • Leukocytes, Mononuclear / immunology
  • Leukocytes, Mononuclear / metabolism
  • Middle Aged
  • Molecular Sequence Annotation
  • Oligonucleotide Array Sequence Analysis
  • Organ Specificity
  • Skin / cytology
  • Skin / immunology
  • Skin / metabolism*
  • T-Lymphocytes, Helper-Inducer / cytology
  • T-Lymphocytes, Helper-Inducer / immunology
  • T-Lymphocytes, Helper-Inducer / metabolism*
  • T-Lymphocytes, Regulatory / cytology
  • T-Lymphocytes, Regulatory / immunology
  • T-Lymphocytes, Regulatory / metabolism*
  • Transcription, Genetic*

Substances

  • Antigens, CD
  • CD8 Antigens
  • Integrin alpha Chains
  • 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.