Phosphoinositides take a central stage in regulating blood platelet production and function

Q1 Biochemistry, Genetics and Molecular Biology Advances in biological regulation Pub Date : 2024-01-01 DOI:10.1016/j.jbior.2023.100992
Sonia Severin , Marie-Pierre Gratacap , Laura Bouvet , Maxime Borret , Afi Oportune Kpotor , Gaëtan Chicanne , Jean-Marie Xuereb , Julien Viaud , Bernard Payrastre
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Abstract

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.

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磷脂酰肌醇在调节血小板的产生和功能方面处于中心阶段。
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发挥着关键作用。这些无核细胞是抗血栓药物的靶点,可以防止它们在心血管疾病中聚集。血小板对生理病理学的各个方面也有重要贡献,包括器官间通讯、愈合、炎症和血栓性炎症。它们的产生和激活受到高度精细化机制的严格调控。其中,涉及肌醇脂质的研究引起了研究人员的注意。磷酸肌醇代表肌醇脂质的肌醇头基的七种组合磷酸化形式。它们通过产生第二信使或直接结合效应蛋白的特定结构域,在调节细胞内机制中发挥着至关重要的作用,如信号转导、肌动蛋白细胞骨架重排和膜运输。在这篇综述中,我们将探讨磷酸肌醇如何与巨核细胞控制血小板产生和血小板活化过程有关。我们还将讨论血小板中磷酸肌醇的多样性,它们在颗粒生物发生和维持以及整合素信号传导中的作用。最后,我们将在人和小鼠血小板的质膜外层发现一个新的磷脂酰肌醇3-单磷酸池。
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来源期刊
Advances in biological regulation
Advances in biological regulation Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
8.90
自引率
0.00%
发文量
41
审稿时长
17 days
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