Zhang Jue, Blackmore Peter F, Hargrave Barbara Y, Xiao Shu, Beebe Stephen J, Schoenbach Karl H
Frank Reidy Research Center for Bioelectrics, Old Dominion University, Norfolk, VA, USA.
Arch Biochem Biophys. 2008 Mar 15;471(2):240-8. doi: 10.1016/j.abb.2007.12.009. Epub 2007 Dec 23.
Nanosecond pulse stimulation of a variety of cells produces a wide range of physiological responses (e.g., apoptosis, stimulation of calcium (Ca2+) fluxes, changes in membrane potential). In this study, we investigated the effect of nanosecond pulses, which generate intense electric fields (nsPEFs), on human platelet aggregation, intracellular free Ca2+ ion concentration ([Ca2+]i) and platelet-derived growth factor release. When platelet rich plasma was pulsed with one 300ns pulse with an electric field of 30kV/cm, platelets aggregated and a platelet gel was produced. Platelet aggregation was observed with pulses as low as 7kV/cm with maximum effects seen with approximately 30kV/cm. The increases in intracellular Ca2+ release and Ca2+ influx were dose dependent on the electrical energy density and were maximally stimulated with approximately 30kV/cm. The increases in [Ca2+]i induced by nsPEF were similar to those seen with thapsigargin but not thrombin. We postulate that nsPEF caused Ca2+ to leak out of intracellular Ca2+ stores by a process involving the formation of nanopores in organelle membranes and also caused Ca2+ influx through plasma membrane nanopores. We conclude that nsPEFs dose-dependently cause platelets to rapidly aggregate, like other platelet agonists, and this is most likely initiated by the nsPEFs increasing [Ca2+]i, however by a different mechanism.
纳秒脉冲刺激多种细胞会产生广泛的生理反应(例如,细胞凋亡、钙(Ca2+)通量刺激、膜电位变化)。在本研究中,我们研究了产生强电场的纳秒脉冲(nsPEFs)对人血小板聚集、细胞内游离Ca2+离子浓度([Ca2+]i)和血小板衍生生长因子释放的影响。当富含血小板的血浆用一个300ns脉冲、电场强度为30kV/cm进行脉冲处理时,血小板聚集并形成血小板凝胶。在低至7kV/cm的脉冲下即可观察到血小板聚集,在约30kV/cm时效果最佳。细胞内Ca2+释放和Ca2+内流的增加与电能密度呈剂量依赖性,在约30kV/cm时受到最大刺激。nsPEF诱导的[Ca2+]i增加与毒胡萝卜素诱导的相似,但与凝血酶诱导的不同。我们推测,nsPEF通过在细胞器膜上形成纳米孔的过程使Ca2+从细胞内Ca2+储存中泄漏出来,并且还通过质膜纳米孔引起Ca2+内流。我们得出结论,nsPEFs像其他血小板激动剂一样,以剂量依赖的方式使血小板迅速聚集,这很可能是由nsPEFs增加[Ca2+]i引发的,不过是通过不同的机制。