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Title: Activated T cells recruit exosomes secreted by dendritic cells via LFA-1.
Author(s): Nolte-'t Hoen, E.N.
Buschow, S.I. (314664947)
Anderton, S.M.
Stoorvogel, W.
Wauben, M.H.M.
Publication year: 2009
Document type: Article / Letter to editor
Journal: Blood
ISSN: 0006-4971
Volume: vol. 113
Issue: iss. 9
Start page: p. 1977
End page: p. 1981
Abstract: 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.
Subject: NCMLS 1B: Immune Regulation
Organization: UMCN Extern
Tumorimmunology
Appears in Collections:Academic bibliography

Please use this identifier to cite or link to this item: http://hdl.handle.net/2066/79542

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