首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >BH3-mimetic ABT-737 induces strong mitochondrial membrane depolarization in platelets but only weakly stimulates apoptotic morphological changes, platelet shrinkage and microparticle formation
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BH3-mimetic ABT-737 induces strong mitochondrial membrane depolarization in platelets but only weakly stimulates apoptotic morphological changes, platelet shrinkage and microparticle formation

机译:模仿BH3的ABT-737在血小板中诱导强烈的线粒体膜去极化,但仅微弱地刺激凋亡的形态变化,血小板收缩和微粒形成

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摘要

Background Depolarization of mitochondrial inner transmembrane potential (ΔΨm) is a key biochemical manifestation of the intrinsic apoptosis pathway in anucleate platelets. Little is known, however, about the relationship between ΔΨm depolarization and downstream morphological manifestations of platelet apoptosis, cell shrinkage and microparticle (MP) formation. Objectives To elucidate this relationship in human platelets. Materials and Methods Using flow cytometry, we analyzed ΔΨm depolarization, platelet shrinkage and MP formation in platelets treated with BH3-mimetic ABT-737 and calcium ionophore A23187, well-known inducers of intrinsic platelet apoptosis. Results We found that at optimal treatment conditions (90 min, 37 C) both ABT-737 and A23187 induce ΔΨm depolarization in the majority (88-94%) of platelets and strongly increase intracellular free calcium. In contrast, effects of A23187 and ABT-737 on platelet shrinkage and MP formation are quite different. A23187 strongly stimulates cell shrinkage and MP formation, whereas ABT-737 only weakly induces these events (10-20% of the effect seen with A23187, P < 0.0001). Conclusions These data indicate that a high level of ΔΨm depolarization and intracellular free calcium does not obligatorily ensure strong platelet shrinkage and MP formation. Since ABT-737 efficiently induces clearance of platelets from the circulation, our results suggest that platelet clearance may occur in the absence of the morphological manifestations of apoptosis. Crown
机译:背景线粒体内部跨膜电位(ΔΨm)的去极化是无核血小板内在凋亡途径的关键生化表现。然而,关于ΔΨm去极化与血小板凋亡,细胞收缩和微粒(MP)形成的下游形态学表现之间的关系知之甚少。目的阐明人血小板中的这种关系。材料和方法使用流式细胞仪,我们分析了BH3模拟ABT-737和钙离子载体A23187(固有的内在性血小板凋亡的诱导剂)处理的血小板中的ΔΨm去极化,血小板收缩和MP形成。结果我们发现,在最佳治疗条件下(90分钟,37°C),ABT-737和A23187均可在大多数(88-94%)血小板中诱导ΔΨm去极化并强烈增加细胞内游离钙。相反,A23187和ABT-737对血小板收缩和MP形成的影响却大不相同。 A23187强烈刺激细胞收缩和MP形成,而ABT-737仅弱诱导这些事件(A23187所见效果的10-20%,P <0.0001)。结论这些数据表明高水平的ΔΨm去极化和细胞内游离钙不能强制性地确保强烈的血小板收缩和MP形成。由于ABT-737有效诱导血小板从循环中清除,我们的结果表明,血小板清除可能会在没有凋亡的形态学表现的情况下发生。王冠

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