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Bruton tyrosine kinase is essential for botrocetin/VWF-induced signaling and GPIb-dependent thrombus formation in vivo.

Abstract
Botrocetin (bt)-facilitated binding of von Willebrand factor (VWF) to the platelet membrane glycoprotein (GP) Ib-IX-V complex on platelets in suspension initiates a signaling cascade that causes alphaIIbbeta3 activation and platelet aggregation. Previous work has demonstrated that bt/VWF-mediated agglutination activates alphaIIbbeta3 and elicits ATP secretion in a thromboxane A2 (TxA2)-dependent manner. The signaling that results in TxA2 production was shown to be initiated by Lyn, enhanced by Src, and propagated through Syk, SLP-76, PI3K, PLCgamma2, and PKC. Here, we demonstrate that the signaling elicited by GPIb-mediated agglutination that results in TxA2 production is dependent on Bruton tyrosine kinase (Btk). The results demonstrate that Btk is downstream of Lyn, Syk, SLP-76, and PI3K; upstream of ERK1/2, PLCgamma2, and PKC; and greatly enhances Akt phosphorylation. The relationship(s), if any, between ERK1/2, PLCgamma2, and PKC were not elucidated. The requirement for Btk and TxA2 receptor function in GPIb-dependent arterial thrombosis was confirmed in vivo by characterizing blood flow in ferric chloride-treated mouse carotid arteries. These results demonstrate that the Btk family kinase, Tec, cannot provide the function(s) missing because of the absence of Btk and that Btk is essential for both bt/VWF-mediated agglutination-induced TxA2 production and GPIb-dependent stable arterial thrombus formation in vivo.
AuthorsJunling Liu, Malinda E Fitzgerald, Michael C Berndt, Carl W Jackson, T Kent Gartner
JournalBlood (Blood) Vol. 108 Issue 8 Pg. 2596-603 (Oct 15 2006) ISSN: 0006-4971 [Print] United States
PMID16788103 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)
Chemical References
  • Crotalid Venoms
  • Platelet Glycoprotein GPIb-IX Complex
  • von Willebrand Factor
  • Thromboxane A2
  • botrocetin
  • Protein-Tyrosine Kinases
  • Agammaglobulinaemia Tyrosine Kinase
  • Btk protein, mouse
  • Phospholipase C gamma
Topics
  • Agammaglobulinaemia Tyrosine Kinase
  • Animals
  • Carotid Artery Thrombosis (blood, etiology)
  • Crotalid Venoms (metabolism)
  • MAP Kinase Signaling System
  • Male
  • Mice
  • Mice, Inbred CBA
  • Mice, Knockout
  • Mice, Mutant Strains
  • Phospholipase C gamma (blood)
  • Phosphorylation
  • Platelet Aggregation (physiology)
  • Platelet Glycoprotein GPIb-IX Complex (metabolism)
  • Protein-Tyrosine Kinases (deficiency, genetics, metabolism)
  • Signal Transduction
  • Thrombosis (blood, etiology)
  • Thromboxane A2 (blood)
  • von Willebrand Factor (metabolism)

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