Institut des Maladies Métaboliques et Cardiovasculaires (I2MC), INSERM UMR-1297 and Université Paul Sabatier, F-31432, Toulouse, France.
Institut des Maladies Métaboliques et Cardiovasculaires (I2MC), INSERM UMR-1297 and Université Paul Sabatier, F-31432, Toulouse, France; Laboratoire d'Hématologie, Centre de Référence des Pathologies Plaquettaires, Centre Hospitalier Universitaire de Toulouse Rangueil, F-31432, Toulouse, France.
Adv Biol Regul. 2024 Jan;91:100992. doi: 10.1016/j.jbior.2023.100992. Epub 2023 Sep 27.
Blood platelets are produced by megakaryocytes through a complex program of differentiation and play a critical role in hemostasis and thrombosis. These anucleate cells are the target of antithrombotic drugs that prevent them from clumping in cardiovascular disease conditions. Platelets also significantly contribute to various aspects of physiopathology, including interorgan communications, healing, inflammation, and thromboinflammation. Their production and activation are strictly regulated by highly elaborated mechanisms. Among them, those involving inositol lipids have drawn the attention of researchers. Phosphoinositides represent the seven combinatorially phosphorylated forms of the inositol head group of inositol lipids. They play a crucial role in regulating intracellular mechanisms, such as signal transduction, actin cytoskeleton rearrangements, and membrane trafficking, either by generating second messengers or by directly binding to specific domains of effector proteins. In this review, we will explore how phosphoinositides are implicated in controlling platelet production by megakaryocytes and in platelet activation processes. We will also discuss the diversity of phosphoinositides in platelets, their role in granule biogenesis and maintenance, as well as in integrin signaling. Finally, we will address the discovery of a novel pool of phosphatidylinositol 3-monophosphate in the outerleaflet of the plasma membrane of human and mouse platelets.
血小板是由巨核细胞通过复杂的分化程序产生的,在止血和血栓形成中起着关键作用。这些无核细胞是抗血栓药物的靶点,这些药物可以防止它们在心血管疾病条件下聚集。血小板还显著参与生理病理的各个方面,包括器官间通讯、愈合、炎症和血栓炎症。它们的产生和激活受到高度精细的机制的严格调节。其中,涉及肌醇脂质的机制引起了研究人员的关注。磷酸肌醇代表肌醇脂质肌醇头部基团的七种组合磷酸化形式。它们通过生成第二信使或直接与效应蛋白的特定结构域结合,在调节细胞内机制(如信号转导、肌动蛋白细胞骨架重排和膜运输)方面发挥着至关重要的作用。在这篇综述中,我们将探讨磷酸肌醇如何参与控制巨核细胞产生血小板和血小板激活过程。我们还将讨论血小板中磷酸肌醇的多样性,它们在颗粒发生和维持以及整合素信号中的作用。最后,我们将讨论在人类和小鼠血小板质膜外层发现一种新的磷脂酰肌醇 3-单磷酸池。