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A new role in hemostasis for the adhesion receptor P-selectin

Journal

TRENDS IN MOLECULAR MEDICINE
Volume 10, Issue 4, Pages 179-186

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.molmed.2004.02.007

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Funding

  1. NHLBI NIH HHS [R37HL41002, R01 HL053756, P01HL56949, R01HL53756, R37 HL041002, P01 HL056949] Funding Source: Medline

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The adhesion receptor P-selectin has long been known to support leukocyte rolling and emigration at sites of inflammation. Recently, P-selectin was also revealed to be a key molecule in hemostasis and thrombosis, mediating platelet rolling, generating procoagulant microparticles containing active tissue factor and enhancing fibrin deposition. Elevated levels of plasma P-selectin are indicative of thrombotic disorders and predictive of future cardiovascular events. Because the interaction between P-selectin and its receptor P-selectin glycoprotein ligand-1 (PSGL-1) represents an important mechanism by which P-selectin induces the formation of procoagulant microparticles and recruits the microparticles to thrombi, anti-thrombotic strategies are currently aimed at inhibiting this interaction. Recent developments also suggest that the procoagulant potential of P-selectin could be used to treat coagulation disorders such as hemophilia A.

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