GPVI levels in platelets: Relationship to platelet function at high shear

Denise Best*, Yotis A. Senis, Gavin E. Jarvis, Helen J. Eagleton, David J. Roberts, Takashi Saito, Stephanie M. Jung, Masaaki Moroi, Paul Harrison, Fiona R. Green, Steve P. Watson

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

118 Citations (Scopus)

Abstract

We have investigated the density of the collagen receptors glycoprotein VI (GPVI) and α2β1 on human platelets and their relationship to polymorphisms within the GPVI gene. GPVI levels varied 1.5-fold and showed a weak correlation (r = 0.35) with the levels of α 2β1, which varied 3-fold. GPVI genotype had a significant effect on receptor levels with carriers of the proline 219 allele (approximately 22% of the population) having 10% lower GPVI levels than the more common serine homozygotes. GPVI and α2β1 levels were found to be significantly decreased on platelets from patients with myeloproliferative disorders (MPDs). In both the MPD and the control group, GPVI levels were found not to affect platelet function under high shear in whole blood. Similarly murine platelets that express up to 5-fold lower levels of GPVI showed no significant difference than controls in thrombus formation on a high-density collagen-coated surface. However platelets lacking the GPVI/Fc receptor γ-chain (FcR γ-chain) complex or a functional FcR γ-chain (immunoreceptor tyrosine-based activation motif [ITAM] point mutant) exhibited severely abrogated thrombus formation at 800 s-1 and 1500 s-1. These results demonstrate that GPVI levels are tightly controlled and play a critical role in thrombus formation on collagen; nevertheless, a range of receptor densities can support platelet function under high shear.

Original languageEnglish
Pages (from-to)2811-2818
Number of pages8
JournalBlood
Volume102
Issue number8
DOIs
Publication statusPublished - 15 Oct 2003
Externally publishedYes

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