Division of Hematology/Oncology, Department of Internal Medicine, University of Iowa, Iowa City, IA.
Blood Adv. 2023 Jun 13;7(11):2347-2359. doi: 10.1182/bloodadvances.2023010100.
Resting platelets rely on oxidative phosphorylation (OXPHOS) and aerobic glycolysis (conversion of glucose to lactate in the presence of oxygen) for their energy requirements. In contrast, platelet activation exhibits an increased rate of aerobic glycolysis relative to OXPHOS. Mitochondrial enzymes pyruvate dehydrogenase kinases (PDKs) phosphorylate the pyruvate dehydrogenase (PDH) complex to inhibit its activity, thereby diverting the pyruvate flux from OXPHOS to aerobic glycolysis upon platelet activation. Of 4 PDK isoforms, PDK2 and PDK4 (PDK2/4) are predominantly associated with metabolic diseases. Herein, we report that the combined deletion of PDK2/4 inhibits agonist-induced platelet functions, including aggregation, integrin αIIbβ3 activation, degranulation, spreading, and clot retraction. In addition, collagen-mediated PLCγ2 phosphorylation and calcium mobilization were significantly reduced in PDK2/4-/- platelets, suggesting impaired GPVI signaling. The PDK2/4-/- mice were less susceptible to FeCl3-induced carotid and laser-induced mesenteric artery thrombosis without any effect on hemostasis. In adoptive transfer experiments, thrombocytopenic hIL-4Rα/GPIbα-transgenic mice transfused with PDK2/4-/- platelets exhibited less susceptibility to FeCl3 injury-induced carotid thrombosis compared with hIL-4Rα/GPIbα-Tg mice transfused with WT platelets, suggesting a platelet-specific role of PDK2/4 in thrombosis. Mechanistically, the inhibitory effects of PDK2/4 deletion on platelet function were associated with reduced PDH phosphorylation and glycoPER in activated platelets, suggesting that PDK2/4 regulates aerobic glycolysis. Finally, using PDK2 or PDK4 single KO mice, we identified that PDK4 plays a more prominent role in regulating platelet secretion and thrombosis compared with PDK2. This study identifies the fundamental role of PDK2/4 in regulating platelet functions and identifies the PDK/PDH axis as a potentially novel antithrombotic target.
静息血小板依赖氧化磷酸化 (OXPHOS) 和有氧糖酵解(在有氧气的情况下将葡萄糖转化为乳酸)来满足其能量需求。相比之下,血小板激活表现出相对于 OXPHOS 更高的有氧糖酵解速率。线粒体酶丙酮酸脱氢酶激酶 (PDK) 使丙酮酸脱氢酶 (PDH) 复合物磷酸化,从而抑制其活性,使血小板激活时丙酮酸通量从 OXPHOS 转向有氧糖酵解。在 4 种 PDK 同工型中,PDK2 和 PDK4(PDK2/4)主要与代谢疾病相关。在此,我们报告 PDK2/4 的联合缺失抑制激动剂诱导的血小板功能,包括聚集、整合素 αIIbβ3 激活、脱粒、扩展和凝块回缩。此外,胶原介导的 PLCγ2 磷酸化和钙动员在 PDK2/4-/-血小板中显著降低,表明 GPVI 信号受损。PDK2/4-/-小鼠对 FeCl3 诱导的颈动脉和激光诱导的肠系膜动脉血栓形成的敏感性降低,而对止血没有任何影响。在过继转移实验中,血小板减少的 hIL-4Rα/GPIbα-转基因小鼠输注 PDK2/4-/-血小板后,对 FeCl3 损伤诱导的颈动脉血栓形成的敏感性低于输注 WT 血小板的 hIL-4Rα/GPIbα-Tg 小鼠,表明 PDK2/4 在血栓形成中具有血小板特异性作用。从机制上讲,PDK2/4 缺失对血小板功能的抑制作用与激活血小板中 PDH 磷酸化和糖酵解减少有关,表明 PDK2/4 调节有氧糖酵解。最后,使用 PDK2 或 PDK4 单 KO 小鼠,我们发现 PDK4 在调节血小板分泌和血栓形成方面比 PDK2 发挥更重要的作用。本研究确定了 PDK2/4 在调节血小板功能中的基本作用,并确定了 PDK/PDH 轴作为一种潜在的新型抗血栓靶点。