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Blood, 15 May 2008, Vol. 111, No. 10, pp. 4958-4964. Prepublished online as a Blood First Edition Paper on February 6, 2008; DOI 10.1182/blood-2007-11-123620.
HEMOSTASIS, THROMBOSIS, AND VASCULAR BIOLOGY Inflammation induces hemorrhage in thrombocytopenia1 Immune Disease Institute and 2 Department of Pathology, Harvard Medical School, Boston, MA; 3 Servei d'Hemoterapia-Hemostasia, Hospital Clinic, Universitat de Barcelona, Spain; and 4 Department of Pediatrics, Harvard Medical School, Boston, MA
The role of platelets in hemostasis is to produce a plug to arrest bleeding. During thrombocytopenia, spontaneous bleeding is seen in some patients but not in others; the reason for this is unknown. Here, we subjected thrombocytopenic mice to models of dermatitis, stroke, and lung inflammation. The mice showed massive hemorrhage that was limited to the area of inflammation and was not observed in uninflamed thrombocytopenic mice. Endotoxin-induced lung inflammation during thrombocytopenia triggered substantial intra-alveolar hemorrhage leading to profound anemia and respiratory distress. By imaging the cutaneous Arthus reaction through a skin window, we observed in real time the loss of vascular integrity and the kinetics of skin hemorrhage in thrombocytopenic mice. Bleeding—observed mostly from venules—occurred as early as 20 minutes after challenge, pointing to a continuous need for platelets to maintain vascular integrity in inflamed microcirculation. Inflammatory hemorrhage was not seen in genetically engineered mice lacking major platelet adhesion receptors or their activators (
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