C-type lectin-like receptor 2 (CLEC-2)-dependent dendritic cell migration is controlled by tetraspanin CD37

Cell migration is central to evoking a potent immune response. Dendritic cell (DC) migration to lymph nodes is dependent on the interaction of C-type lectin-like receptor 2 (CLEC-2; encoded by the gene ), expressed by DCs, with podoplanin, expressed by lymph node stromal cells, although the underlyi...

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Veröffentlicht in:Journal of cell science 2018-10, Vol.131 (19)
Hauptverfasser: de Winde, Charlotte M, Matthews, Alexandra L, van Deventer, Sjoerd, van der Schaaf, Alie, Tomlinson, Neil D, Jansen, Erik, Eble, Johannes A, Nieswandt, Bernhard, McGettrick, Helen M, Figdor, Carl G, Tomlinson, Michael G, Acton, Sophie E, van Spriel, Annemiek B
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Sprache:eng
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Zusammenfassung:Cell migration is central to evoking a potent immune response. Dendritic cell (DC) migration to lymph nodes is dependent on the interaction of C-type lectin-like receptor 2 (CLEC-2; encoded by the gene ), expressed by DCs, with podoplanin, expressed by lymph node stromal cells, although the underlying molecular mechanisms remain elusive. Here, we show that CLEC-2-dependent DC migration is controlled by tetraspanin CD37, a membrane-organizing protein. We identified a specific interaction between CLEC-2 and CD37, and myeloid cells lacking CD37 ( ) expressed reduced surface CLEC-2. CLEC-2-expressing DCs showed impaired adhesion, migration velocity and displacement on lymph node stromal cells. Moreover, DCs failed to form actin protrusions in a 3D collagen matrix upon podoplanin-induced CLEC-2 stimulation, phenocopying CLEC-2-deficient DCs. Microcontact printing experiments revealed that CD37 is required for CLEC-2 recruitment in the membrane to its ligand podoplanin. Finally, DCs failed to inhibit actomyosin contractility in lymph node stromal cells, thus phenocopying CLEC-2-deficient DCs. This study demonstrates that tetraspanin CD37 controls CLEC-2 membrane organization and provides new molecular insights into the mechanisms underlying CLEC-2-dependent DC migration.This article has an associated First Person interview with the first author of the paper.
ISSN:1477-9137
DOI:10.1242/jcs.214551