A CD26-controlled cell surface cascade for regulation of T cell motility and chemokine signals

J Immunol. 2009 Sep 15;183(6):3616-24. doi: 10.4049/jimmunol.0804336. Epub 2009 Aug 17.

Abstract

Chemokines are key regulators of cell trafficking, and dipeptidyl peptidase IV/CD26 (CD26) inactivates chemokines. Here we show that the CD26-processed chemokines SDF1alpha/CXCL12 and RANTES/CCL5, in contrast to a control chemokine not processed by CD26, are potent inducers of cell surface expression of thrombospondin-1 (TSP-1) in T lymphocytes through a CD26-controlled mechanism and that TSP-1 stimulates expression of lipoprotein receptor related protein/CD91. Accordingly, intact TSP-1 and a peptide mimetic of a sequence in TSP-1 were sufficient to stimulate CD91 expression. The chemokine-induced expression of TSP-1 and CD91 was mimicked by inhibitors of CD26 and CXCL12 and CCL5 as well as inhibitors of CD26 stimulated polarized cytoplasmic spreading and migration through TSP-1. Silencing of CD26 using small interfering RNA or Ab-induced modulation of CD26 also increased TSP-1 expression and enhanced cytoplasmic spreading and T cell migration markedly. These results indicate that CD26 is an endogenous inhibitor of T cell motility through inhibition of TSP-1 expression and that chemokines stimulate cell polarity and migration through abrogation of the CD26-dependent inhibition. This suggests that T cell motility is regulated by a cascade of interacting cell surface molecules.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cells, Cultured
  • Chemokine CCL5 / metabolism
  • Chemokine CXCL12 / metabolism
  • Chemokines / metabolism*
  • Chemotaxis, Leukocyte*
  • Dipeptidyl Peptidase 4 / physiology*
  • Gene Expression Regulation / immunology
  • Humans
  • Membrane Proteins / metabolism*
  • Signal Transduction / immunology*
  • T-Lymphocytes / physiology
  • Thrombospondin 1 / genetics*

Substances

  • CCL5 protein, human
  • Chemokine CCL5
  • Chemokine CXCL12
  • Chemokines
  • Membrane Proteins
  • Thrombospondin 1
  • Dipeptidyl Peptidase 4