Disulfide HMGB1 derived from platelets coordinates venous thrombosis in mice.

@article{Stark2016DisulfideHD,
  title={Disulfide HMGB1 derived from platelets coordinates venous thrombosis in mice.},
  author={Konstantin Stark and Vanessa Philippi and Sven Stockhausen and Johanna Busse and Antonella Antonelli and Meike Miller and Irene Schubert and Parandis Hoseinpour and Sue Chandraratne and Marie-Luise von Bruehl and Florian Gaertner and Michael Lorenz and Alessandra Agresti and Raffaele Coletti and Daniel J Antoine and Ralf Heermann and Kirsten Jung and S. Reese and Iina Laitinen and Markus Schwaiger and Axel Walch and Markus Sperandio and Peter P Nawroth and Christoph Reinhardt and Sven J{\"a}ckel and Marco Emilio Bianchi and Steffen Massberg},
  journal={Blood},
  year={2016},
  volume={128 20},
  pages={2435-2449}
}
Deep venous thrombosis (DVT) is one of the most common cardiovascular diseases, but its pathophysiology remains incompletely understood. Although sterile inflammation has recently been shown to boost coagulation during DVT, the underlying molecular mechanisms are not fully resolved, which could potentially identify new anti-inflammatory approaches to prophylaxis and therapy of DVT. Using a mouse model of venous thrombosis induced by flow reduction in the vena cava inferior, we identified blood… CONTINUE READING

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