Ravera Silvia, Signorello Maria Grazia, Bartolucci Martina, Ferrando Sara, Manni Lucia, Caicci Federico, Calzia Daniela, Panfoli Isabella, Morelli Alessandro, Leoncini Giuliana
Department of Pharmacy, Biochemistry Lab, University of Genova, Genova, 16132, Italy.
Dipartimento di Scienze della Terra, dell'Ambiente e della Vita (DISTAV), University of Genoa, Genoa, 16132, Italy.
Biol Cell. 2018 May;110(5):97-108. doi: 10.1111/boc.201700025. Epub 2018 Apr 16.
Energy demand in human platelets is very high, to carry out their functions. As for most human cells, the aerobic metabolism represents the primary energy source in platelets, even though mitochondria are negligibly represented. Following the hypothesis that other structures could be involved in chemical energy production, in this work, we have investigated the functional expression of an extramitochondrial aerobic metabolism in platelets.
Oximetric and luminometric analyses showed that platelets consume large amounts of oxygen and produce ATP in the presence of common respiring substrates, such as pyruvate + malate or succinate, although morphological electron microscopy analysis showed that these contain few mitochondria. However, evaluation of the anaerobic glycolytic metabolism showed that only 13% of consumed glucose was converted to lactate. Interestingly, the highest OXPHOS activity was observed in the presence of NADH, not a readily permeant respiring substrate for mitochondria. Also, oxygen consumption and ATP synthesis fuelled by NADH were not affected by atractyloside, an inhibitor of the adenine nucleotide translocase, suggesting that these processes may not be ascribed to mitochondria. Functional data were confirmed by immunofluorescence microscopy and Western blot analyses, showing a consistent expression of the β subunit of F F -ATP synthase and COXII, a subunit of Complex IV, but a low signal of translocase of the inner mitochondrial membrane (a protein not involved in OXPHOS metabolism). Interestingly, the NADH-stimulated oxygen consumption and ATP synthesis increased in the presence of the physiological platelets agonists, thrombin or collagen.
Data suggest that in platelets, aerobic energy production is mainly driven by an extramitochondrial OXPHOS machinery, originated inside the megakaryocyte, and that this metabolism plays a pivotal role in platelet activation.
This work represents a further example of the existence of an extramitochondrial aerobic metabolism, which can contribute to the cellular energy balance.
人类血小板的能量需求非常高,以执行其功能。与大多数人类细胞一样,尽管线粒体的数量极少,但有氧代谢仍是血小板的主要能量来源。基于其他结构可能参与化学能产生的假设,在本研究中,我们调查了血小板中线粒体外有氧代谢的功能表达。
血氧测定和发光分析表明,血小板在存在常见呼吸底物(如丙酮酸 + 苹果酸或琥珀酸)的情况下消耗大量氧气并产生ATP,尽管形态学电子显微镜分析显示这些底物中含有少量线粒体。然而,对无氧糖酵解代谢的评估表明,只有13% 的消耗葡萄糖转化为乳酸。有趣的是,在存在NADH(一种线粒体不易通透的呼吸底物)的情况下观察到最高的氧化磷酸化活性。此外,由NADH 驱动的氧气消耗和ATP 合成不受腺嘌呤核苷酸转位酶抑制剂苍术苷的影响,这表明这些过程可能不归因于线粒体。免疫荧光显微镜和蛋白质印迹分析证实了功能数据,显示F₁F₀ -ATP合酶的β亚基和复合物IV的亚基COXII有一致的表达,但线粒体内膜转位酶(一种不参与氧化磷酸化代谢的蛋白质)的信号较低。有趣的是,在生理性血小板激动剂凝血酶或胶原蛋白存在的情况下,NADH刺激的氧气消耗和ATP合成增加。
数据表明,在血小板中,有氧能量产生主要由源自巨核细胞内部的线粒体外氧化磷酸化机制驱动,并且这种代谢在血小板激活中起关键作用。
这项工作代表了线粒体外有氧代谢存在的又一个例子,它可以有助于细胞能量平衡。