GPVI and CLEC-2 in haemostasis and vascular integrity

Steve Watson, John Herbert, Alice Pollitt

Research output: Contribution to journalArticle

128 Citations (Scopus)


Summary The GPVI-FcR gamma-chain complex initiates powerful activation of platelets by the subendothelial matrix proteins collagen and laminin through an immunoreceptor tyrosine-based activation motif (ITAM)-regulated signalling pathway. ITAMs are characterised by two YxxL sequences separated by 6-12 amino acids and are found associated with several classes of immunoglobulin (Ig) and C-type lectin receptors in haematopoietic cells, including Fc receptors. Crosslinking of the Ig GPVI leads to phosphorylation of two conserved tyrosines in the FcR gamma-chain ITAM by Src family tyrosine kinases, followed by binding and activation of the tandem SH2 domain-containing Syk tyrosine kinase, and stimulation of a downstream signalling cascade that culminates in activation of phospholipase Cgamma2 (PLCgamma2). In contrast, the C-type lectin receptor CLEC-2 mediates powerful platelet activation through Src and Syk kinases, but regulates Syk through a novel dimerisation mechanism via a single YxxL motif known as a hemITAM. CLEC-2 is a receptor for podoplanin, which is expressed at high level in several tissues, including type 1 lung alveolar cells, lymphatic endothelial cells, kidney podocytes and some tumours, but is absent from vascular endothelial cells and platelets. In this article, we compare the mechanism of platelet activation by GPVI and CLEC-2 and consider their functional roles in haemostasis and other vascular processes, including maintenance of vascular integrity, angiogenesis and possibly lymphogenesis.
Original languageEnglish
JournalJournal of Thrombosis and Haemostasis
Publication statusPublished - 1 Mar 2010


  • CLEC-2
  • platelets
  • Src and Syk tyrosine kinases
  • ITAM
  • hemITAM
  • GPVI-FcR gamma-chain


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