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

Cell Tissue Res. 2013 Jun;352(3):695-705. doi: 10.1007/s00441-013-1618-6. Epub 2013 May 4.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

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

Substances

  • Cre recombinase
  • Integrases
  • Septins
  • septin 9, mouse