Key role of integrin alpha(IIb)beta(3) signaling to Syk kinase in tissue factor-induced thrombin generation


van der Meijden P. E. J. , Feijge M. A. H. , Swieringa F., Gilio K., Nergiz-Unal R. , Hamulyak K., ...Daha Fazla

CELLULAR AND MOLECULAR LIFE SCIENCES, cilt.69, ss.3481-3492, 2012 (SCI İndekslerine Giren Dergi) identifier identifier identifier

  • Cilt numarası: 69 Konu: 20
  • Basım Tarihi: 2012
  • Doi Numarası: 10.1007/s00018-012-1033-2
  • Dergi Adı: CELLULAR AND MOLECULAR LIFE SCIENCES
  • Sayfa Sayıları: ss.3481-3492

Özet

The fibrin(ogen) receptor, integrin alpha(IIb)beta(3), has a well-established role in platelet spreading, aggregation and clot retraction. How alpha(IIb)beta(3) contributes to platelet-dependent coagulation is less well resolved. Here, we demonstrate that the potent suppressing effect of clinically used alpha(IIb)beta(3) blockers on tissue factor-induced thrombin generation is linked to diminished platelet Ca2+ responses and phosphatidylserine (PS) exposure. The same blockers suppress these responses in platelets stimulated with collagen and thrombin receptor agonists, whereas added fibrinogen potentiates these responses. In platelets spreading on fibrinogen, outside-in alpha(IIb)beta(3) signaling similarly enhances thrombin-induced Ca2+ rises and PS exposure. These responses are reduced in alpha(IIb)beta(3)-deficient platelets from patients with Glanzmann's thrombasthenia. Furthermore, the contribution of alpha(IIb)beta(3) to tissue factor-induced platelet Ca2+ rises, PS exposure and thrombin generation in plasma are fully dependent on Syk kinase activity. Tyrosine phosphorylation analysis confirms a key role of Syk activation, which is largely but not exclusively dependent on alpha(IIb)beta(3) activation. It is concluded that the majority of tissue factor-induced procoagulant activity of platelets relies on Syk activation and ensuing Ca2+ signal generation, and furthermore that a considerable part of Syk activation relies on alpha(IIb)beta(3) signaling. These results hence point to a novel role of Syk in integrin-dependent thrombin generation.