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Crawley, J. T.

Publications and source records attributed to Crawley, J. T..

2 recordsLinked to original sources

The GPIbα intracellular tail - role in transducing VWF- and Collagen/GPVI-mediated signaling

Synergy between GPIb and GPVI signaling machineries has been suggested previously, however its molecular mechanism remains unclear. We generated a novel GPIb transgenic mouse (GPIb{Delta}sig/{Delta}sig) by CRISPR-Cas9 technology to delete the last 24 residues of the GPIb intracellular tail important for VWF-mediated signaling. GPIb{Delta}sig/{Delta}sig platelets bound VWF normally under flow but formed fewer filopodia on VWF/botrocetin, demonstrating that the deleted region does not affect ligand binding but appreciably impairs VWF-dependent signaling. Notably, while haemostasis was normal in GPIb{Delta}sig/{Delta}sig mice, GPIb{Delta}sig/{Delta}sig platelets exhibited defective responses after collagen-related-peptide stimulation and formed smaller aggregates on collagen-coated microchannels at low and high shears. Flow assays performed with plasma-free blood or in the presence of IIb{beta}3-or GPVI-blockers suggested reduced IIb{beta}3 activation contributes to the phenotype of the GPIb{Delta}sig/{Delta}sig platelets. Together, these results reveal a new role for the intracellular tail of GPIb in transducing both VWF-GPIb and collagen-GPVI signaling events in platelets. Summary statementGPIb and GPVI are two key receptors on the platelet surface. Using a novel transgenic mouse (GPIb{Delta}sig/{Delta}sig) that lacks the last 24 amino acids of the GPIb intracellular tail, we demonstrate the importance of this region not only in transducing signals in response to GPIb binding to VWF, but also for collagen-GPVI-mediated platelet responses revealing previously underappreciated receptor crosstalk between GPIb and GPVI.

cell biology↗

Novel platelet-neutrophil interaction via activated αIIbβ3 mediates NETosis under flow

Platelet-neutrophil interactions are important for innate immunity, but also contribute to the pathogenesis of deep vein thrombosis, myocardial infarction and stroke. Here we report that, under flow, von Willebrand factor/glycoprotein Ib-dependent platelet priming induces integrin IIb{beta}3 activation that, in turn, mediates neutrophil and T-cell binding. Binding of platelet IIb{beta}3 to SLC44A2 on neutrophils leads to mechanosensitive-dependent production of highly prothrombotic neutrophil extracellular traps. A polymorphism in SLC44A2 (rs2288904-A) present in 22% of the population causes an R154Q substitution in an extracellular loop of SLC44A2 that is protective against venous thrombosis results in severely impaired binding to both activated IIb{beta}3 and VWF-primed platelets. This was confirmed using neutrophils homozygous for the SLC44A2 R154Q polymorphism. Taken together, these data reveal a previously unreported mode of platelet-neutrophil cross-talk, mechanosensitive NET production, and provide mechanistic insight into the protective effect of the SLC44A2 rs2288904-A polymorphism in venous thrombosis.\n\nSummaryPlatelets that are primed following interaction with von Willebrand factor under flow mediated direct interactions with neutrophils via activated platelet integrin, IIb{beta}3, and SLC44A2 on neutrophils. This interaction initiates signaling in a mechanosensitive manner that promotes neutrophil extracellular trap formation.

cell biology↗