Activated T cells recruit exosomes secreted by dendritic cells via LFA-1

Esther N. M. Nolte-'t Hoen, Sonja I. Buschow, Stephen M. Anderton, Willem Stoorvogel, Marca H. M. Wauben

Research output: Contribution to journalArticlepeer-review

Abstract / Description of output

Dendritic cells (DCs) are known to secrete exosomes that transfer membrane proteins, like major histocompatibility complex class II, to other DCs. Intercellular transfer of membrane proteins is also observed during cognate interactions between DCs and CD4(+) T cells. The acquired proteins are functional and play a role in regulation of immune responses. How membrane protein transfer is achieved and regulated is unclear. Here we show that T cells can recruit major histocompatibility complex class II containing DC exosomes secreted in the extracellular milieu during cognate DC T-cell interactions. Recruitment of these exosomes required T-cell activation and was dependent on leukocyte function associated antigen-1 (LFA-1) rather than on T-cell receptor specificity. Indeed, inducing a high-affinity state of LFA-1 on resting T cells was sufficient to provoke exosome binding. These results imply that DC exosomes secreted in the extracellular milieu during cognate T-cell-DC interactions are targeted to T cells activated in that microenvironment. (Blood. 2009; 113: 1977-1981)

Original languageEnglish
Pages (from-to)1977-1981
Number of pages5
JournalBlood
Volume113
Issue number9
DOIs
Publication statusPublished - 26 Feb 2009

Keywords / Materials (for Non-textual outputs)

  • Animals
  • CD4-Positive T-Lymphocytes
  • Cattle
  • Cell Communication
  • Cells, Cultured
  • Dendritic Cells
  • Exosomes
  • Genes, p53
  • Intercellular Adhesion Molecule-1
  • Lymphocyte Activation
  • Lymphocyte Function-Associated Antigen-1
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Protein Binding

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