Department of Biochemistry, Louisiana State University Health Sciences Center, MEB-7114, New Orleans, LA, 70112, USA.
J Membr Biol. 2022 Dec;255(6):733-737. doi: 10.1007/s00232-022-00265-7. Epub 2022 Sep 13.
Blood coagulation is an intricate process, and it requires precise control of the activities of pro- and anticoagulant factors and sensitive signaling systems to monitor and respond to blood vessel insults. These requirements are fulfilled by phosphatidylserine, a relatively miniscule-sized lipid molecule amid the myriad of large coagulation proteins. This review limelight the role of platelet membrane phosphatidylserine (PS) in regulating a key enzymatic reaction of blood coagulation; conversion of factor X to factor Xa by the enzyme factor IXa and its cofactor factor VIIIa. PS is normally located on the inner leaflet of the resting platelet membrane but appears on the outer leaflet surface of the membrane surface after an injury happens. Human platelet activation leads to exposure of buried PS molecules on the surface of the platelet-derived membranes and the exposed PS binds to discrete and specific sites on factors IXa and VIIIa. PS binding to these sites allosterically regulates both factors IXa and VIIIa. The exposure of PS and its binding to factors IXa/VIIIa is a vital step during clotting. Insufficient exposure or a defective binding of PS to these clotting proteins is responsible for various hematologic diseases which are discussed in this review.
血液凝固是一个复杂的过程,需要精确控制促凝和抗凝因子的活性以及敏感的信号系统,以监测和应对血管损伤。这些要求由磷脂酰丝氨酸(PS)来满足,PS 是一种相对微小的脂质分子,存在于众多大型凝血蛋白之间。本综述重点介绍血小板膜磷脂酰丝氨酸(PS)在调节血液凝固关键酶反应中的作用;即酶因子 IXa 和其辅因子因子 VIIIa 将因子 X 转化为因子 Xa。PS 通常位于静止血小板膜的内小叶,但在发生损伤后会出现在膜表面的外小叶。人类血小板激活导致埋藏在血小板衍生膜表面的 PS 分子暴露,暴露的 PS 与因子 IXa 和 VIIIa 上的离散和特定位点结合。PS 与这些位点的结合变构调节因子 IXa 和 VIIIa。PS 的暴露及其与因子 IXa/VIIIa 的结合是凝血过程中的一个重要步骤。PS 暴露不足或与这些凝血蛋白结合缺陷会导致各种血液疾病,本综述对此进行了讨论。