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Defective Signal Transduction through the Thromboxane A2 Receptor in a Patient with a Miid Bleeding Disorder: Deficiency of the Inositol 1,4,5-Triphosphate Formation despite Normal G-protein Activation
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1997
Year
PathologyMild Bleeding DisorderPharmacotherapyThrombosisHematologyNeurologyBleeding DisorderPlatelet AntagonistAtherosclerosisMiid Bleeding DisorderProlonged Bleeding TimeVascular BiologyDefective Signal TransductionPharmacologyPlatelet ActivationThrombopoiesisSignal TransductionBlood PlateletThromboxane A2 ReceptorHemostasisPlatelet Txa2 ReceptorCoagulopathyMedicine
We describe an 11-year-old girl with a mild bleeding disorder since early childhood. The disorder was characterized by a prolonged bleeding time, and the patient's platelets showed defective aggregation responses to thromboxane A2 (TXA2) mimetic U46619 and arachidonic acid. In contrast, the platelets showed normal responses to thrombin and Ca ionophore A23187. When the platelet TXA2 receptor was examined with the [3H]-labeled TXA2 agonist U46619, the equilibrium dissociation rate constants (kd) and the maximal concentration of binding sites (Bmax) of the patient's platelets were within normal ranges. Normal GTPase activity was also induced in the patient's platelets by stimulation with U46619, however, inositol 1,4,5-triphosphate (IP3) formation was not induced by U46619. These results suggests that the patient's platelets had a defect in phospholipase C activation beyond TXA2 receptors.