Glycoprotein VI is not a Functional Platelet Receptor for Fibrin Formed in Plasma or Blood.
Agammaglobulinaemia Tyrosine Kinase
/ blood
Blood Platelets
/ metabolism
Enzyme Activation
Fibrin
/ metabolism
Fibrinogen
/ metabolism
Hemorheology
Humans
Microscopy, Confocal
/ methods
Plasma
Platelet Adhesiveness
Platelet Aggregation
Platelet Glycoprotein GPIb-IX Complex
/ metabolism
Platelet Membrane Glycoproteins
/ antagonists & inhibitors
Protein Binding
Receptors, Peptide
/ metabolism
Recombinant Proteins
/ metabolism
Syk Kinase
/ antagonists & inhibitors
Thromboplastin
/ metabolism
Journal
Thrombosis and haemostasis
ISSN: 2567-689X
Titre abrégé: Thromb Haemost
Pays: Germany
ID NLM: 7608063
Informations de publication
Date de publication:
Jun 2020
Jun 2020
Historique:
entrez:
4
6
2020
pubmed:
4
6
2020
medline:
13
7
2021
Statut:
ppublish
Résumé
Glycoprotein VI (GPVI), a platelet collagen receptor, is crucial in mediating atherothrombosis. Besides collagen, injured plaques expose tissue factor (TF) that triggers fibrin formation. Previous studies reported that GPVI also is a platelet receptor for fibrinogen and fibrin. We studied the effect of anti-GPVI antibodies and inhibitors of GPVI signaling kinases (Syk and Btk) on platelet adhesion and aggregate formation onto immobilized fibrinogen and different types of fibrin under arterial flow conditions. Fibrin was prepared from isolated fibrinogen ("pure fibrin"), recombinant fibrinogen ("recombinant fibrin"), or generated more physiologically from endogenous fibrinogen in plasma ("plasma fibrin") or by exposing TF-coated surfaces to flowing blood ("blood fibrin"). Inhibition of GPVI and Syk did not inhibit platelet adhesion and aggregate formation onto fibrinogen. In contrast anti-GPVI antibodies, inhibitors of Syk and Btk and the anti-GPIb antibody 6B4 inhibited platelet aggregate formation onto pure and recombinant fibrin. However, inhibition of GPVI and GPVI signaling did not significantly reduce platelet coverage of plasma fibrin and blood fibrin. Plasma fibrin contained many proteins incorporated during clot formation. Advanced optical imaging revealed plasma fibrin as a spongiform cushion with thicker, knotty, and long fibers and little activation of adhering platelets. Albumin intercalated in plasma fibrin fibers left only little space for platelet attachment. Pure fibrin was different showing a dense mesh of thin fibers with strongly activated platelets. We conclude that fibrin formed in plasma and blood contains plasma proteins shielding GPVI-activating epitopes. Our findings do not support a role of GPVI for platelet activation by physiologic fibrin.
Identifiants
pubmed: 32492725
doi: 10.1055/s-0040-1710012
doi:
Substances chimiques
Platelet Glycoprotein GPIb-IX Complex
0
Platelet Membrane Glycoproteins
0
Receptors, Peptide
0
Recombinant Proteins
0
fibrin receptor
0
platelet membrane glycoprotein VI
0
Fibrin
9001-31-4
Fibrinogen
9001-32-5
Thromboplastin
9035-58-9
Agammaglobulinaemia Tyrosine Kinase
EC 2.7.10.2
BTK protein, human
EC 2.7.10.2
SYK protein, human
EC 2.7.10.2
Syk Kinase
EC 2.7.10.2
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
977-993Subventions
Organisme : AZ 1145-14
ID : Bayerische Forschungsstiftung
Organisme : SFB1123/Z01
ID : Deutsche Forschungsgemeinschaft
Organisme : SFB1123/B08
ID : Deutsche Forschungsgemeinschaft
Informations de copyright
Georg Thieme Verlag KG Stuttgart · New York.
Déclaration de conflit d'intérêts
K.A. and K.U. are employees of advanceCOR GmbH which produces the anti-GPVI antibodies. G.M. and M.U. are managing directors of advanceCOR GmbH and own shares of the company. The other authors report no conflict of interest.