Ravi Saranya, Chacko Balu, Kramer Philip A, Sawada Hirotaka, Johnson Michelle S, Zhi Degui, Marques Marisa B, Darley-Usmar Victor M
Department of Pathology, University of Alabama at Birmingham, Birmingham, AL, USA; UAB Mitochondrial Medicine Laboratory, University of Alabama at Birmingham, Birmingham, AL, USA; Center for Free Radical Biology, University of Alabama at Birmingham, Birmingham, AL, USA.
Department of Biostatistics, University of Alabama at Birmingham, Birmingham, AL, USA.
Biochim Biophys Acta. 2015 Nov;1852(11):2525-34. doi: 10.1016/j.bbadis.2015.08.026. Epub 2015 Aug 29.
The quality of platelets decreases over storage time, shortening their shelf life and potentially worsening transfusion outcomes. The changes in mitochondrial function associated with platelet storage are poorly defined and to address this we measured platelet bioenergetics in freshly isolated and stored platelets. We demonstrate that the hypotonic stress test stimulates both glycolysis and oxidative phosphorylation and the stored platelets showed a decreased recovery to this stress. We found no change in aggregability between the freshly isolated and stored platelets. Bioenergetic parameters were changed including increased proton leak and decreased basal respiration and this was reflected in a lower bioenergetic health index (BHI). Mitochondrial electron transport, measured in permeabilized platelets, showed only minor changes which are unlikely to have a significant impact on platelet function. There were no changes in basal glycolysis between the fresh and stored platelets, however, glycolytic rate was increased in stored platelets when mitochondrial ATP production was inhibited. The increase in proton leak was attenuated by the addition of albumin, suggesting that free fatty acids could play a role in increasing proton leak and decreasing mitochondrial function. In summary, platelet storage causes a modest decrease in oxidative phosphorylation driven by an increase in mitochondrial proton leak, which contributes to the decreased recovery to hypotonic stress.
血小板的质量会随着储存时间的延长而下降,缩短其保质期,并可能使输血效果恶化。与血小板储存相关的线粒体功能变化尚不明确,为了解决这一问题,我们测量了新鲜分离和储存的血小板的生物能量学。我们证明,低渗应激试验会刺激糖酵解和氧化磷酸化,而储存的血小板对这种应激的恢复能力下降。我们发现新鲜分离的血小板和储存的血小板之间的聚集性没有变化。生物能量学参数发生了改变,包括质子泄漏增加和基础呼吸减少,这反映在较低的生物能量健康指数(BHI)上。在透化血小板中测量的线粒体电子传递仅显示出微小变化,不太可能对血小板功能产生重大影响。新鲜血小板和储存血小板之间的基础糖酵解没有变化,然而,当线粒体ATP生成受到抑制时,储存血小板中的糖酵解速率增加。添加白蛋白可减弱质子泄漏的增加,这表明游离脂肪酸可能在增加质子泄漏和降低线粒体功能中发挥作用。总之,血小板储存会导致线粒体质子泄漏增加,从而适度降低氧化磷酸化,这导致对低渗应激的恢复能力下降。