Septin9 is involved in T-cell development and CD8+ T-cell homeostasis

Louise Berkhoudt Lassen, Annette C. Füchtbauer, Alexander Schmitz, Annette Balle Sørensen, Finn Skou Pedersen, Ernst-Martin Füchtbauer

Research output: Contribution to journalJournal articleResearchpeer-review

13 Citations (Scopus)

Abstract

SEPTIN9 (SEPT9) is a filament-forming protein involved in numerous cellular processes. We have used a conditional knock out allele of Sept9 to specifically delete Sept9 in T-cells. As shown by fluorescence-activated cell sorting, loss of Sept9 at an early thymocyte stage in the thymus results in increased numbers of double-negative cells indicating that SEPT9 is involved in the transition from the double-negative stage during T-cell development. Accordingly, the relative numbers of mature T-cells in the periphery are decreased in mice with a T-cell-specific deletion of Sept9. Proliferation of Sept9-deleted CD8(+) T-cells from the spleen is decreased upon stimulation in culture. The altered T-cell homeostasis caused by the loss of Sept9 results in an increase of CD8(+) central memory T-cells.
Original languageEnglish
JournalCell and Tissue Research
Volume352
Issue number3
Pages (from-to)695-705
Number of pages11
ISSN0302-766X
DOIs
Publication statusPublished - Jun 2013

Keywords

  • Animals
  • CD8-Positive T-Lymphocytes
  • Cell Count
  • Cell Differentiation
  • Cell Proliferation
  • Down-Regulation
  • Homeostasis
  • Immunologic Memory
  • Integrases
  • Lymphocyte Depletion
  • Lymphoid Tissue
  • Mice
  • Mice, Knockout
  • Real-Time Polymerase Chain Reaction
  • Septins
  • Up-Regulation

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