Proceedings of the National Academy of Sciences · 2002 · 474 citations · 30 references
Life SciencesHematologyImmunologyImmunopathologyInflammationInnate ImmunityLeukocyte AdhesionLeukocyte RecruitmentLeukocyte TraffickingRed Blood Cell DisordersRed Blood Cell PhysiologySickle Cell DiseaseEndothelial-leukocyte InteractionsHemoglobin FunctionIntravital MicroscopyLeukocyte Adhesion MoleculesSickle Cell AnemiaSickle Cell Hemoglobin PhysiologyVascular Endothelial InteractionsVessel Wall Structure
Vascular occlusion is the major cause of morbidity and mortality in sickle cell disease but its mechanisms are poorly understood. We demonstrate by using intravital microscopy in mice expressing human sickle hemoglobin (SS) that SS red blood cells (RBCs) bind to adherent leukocytes in inflamed venules, producing vasoocclusion of cremasteric venules. SS mice deficient in P- and E-selectins, which display defective leukocyte recruitment to the vessel wall, are protected from vasoocclusion. These data uncover a previously unsuspected paradigm for the pathogenesis of sickle cell vasoocclusion in which adherent leukocytes play a direct role and suggest that drugs targeting SS RBC-leukocyte or leukocyte-endothelial interactions may prevent or treat the vascular complications of this debilitating disease.
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Causes and Outcomes of the Acute Chest Syndrome in Sickle Cell Disease
Elliott Vichinsky, Lynne Neumayr, Ann N. Earles et al. · New England Journal of Medicine · 2000 · 1.2K citations · Full text
Medicine, Cardiology, Hematology +7
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