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The value of proteomics for the diagnosis of a platelet-related bleeding disorder.
Maurer-Spurej, E; Kahr, W H; Carter, C J; Pittendreigh, C; Cameron, M; Cyr, T D.
Afiliación
  • Maurer-Spurej E; Canadian Blood Services, Vancouver, BC, Canada. emaurer@interchange.ubc.ca
Platelets ; 19(5): 342-51, 2008 Aug.
Article en En | MEDLINE | ID: mdl-18791940
Familial bleeding problems are frequently difficult to diagnose because currently used clinical tests cannot identify intracellular molecular defects of platelets. Using platelet proteomics, a comprehensive analytical tool, we diagnosed a family with severe bleeding problems of unknown origin with Quebec Platelet Disorder. Prior to proteomic analysis, we determined platelet counts, presence of glycoprotein (GP) Ib and GPIIb/IIIa, platelet aggregation, dense granule content and release, plasma levels of fibrinogen, Factor XIII and fibrin degradation products in four family members. Abnormalities were detected in platelet aggregation studies, which revealed variably reduced responses to ADP, collagen and epinephrine with concomitantly decreased ATP/serotonin secretion. In addition, D-dimer levels were significantly elevated 72 hours after in vitro thrombin stimulation of platelet-rich plasma. Together with the autosomal dominant inheritance and the delayed onset of bleeding in two of the four patients these results did not support any known platelet disorder. Therefore, the proteome of platelet lysates separated by one-dimensional SDS-PAGE was analysed by liquid chromatography-tandem mass spectrometry (LC-MS/MS). Platelet proteomics showed reduced amounts of alpha-granule proteins multimerin, fibrinogen and thrombospondin-1 in patient compared to control samples suggestive of Quebec Platelet Disorder. The diagnosis of Quebec Platelet Disorder was confirmed by urokinase-specific Western blots. Urokinase causes the degradation of alpha-granule proteins in this disorder. Diagnosis of rare bleeding disorders has important implications for prophylactic and acute treatment of bleeding patients. This is the first report using proteomics to identify a familial platelet defect.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Plaquetas / Proteínas Sanguíneas / Activador de Plasminógeno de Tipo Uroquinasa / Gránulos Citoplasmáticos / Proteómica / Trastornos Hemorrágicos Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Male País/Región como asunto: America do norte Idioma: En Revista: Platelets Asunto de la revista: HEMATOLOGIA Año: 2008 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Plaquetas / Proteínas Sanguíneas / Activador de Plasminógeno de Tipo Uroquinasa / Gránulos Citoplasmáticos / Proteómica / Trastornos Hemorrágicos Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Male País/Región como asunto: America do norte Idioma: En Revista: Platelets Asunto de la revista: HEMATOLOGIA Año: 2008 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Reino Unido