Institut des Maladies Métaboliques et Cardiovasculaires (I2MC), INSERM UMR-1297, Université Paul Sabatier, F-31432 Toulouse Cedex, France.
Laboratoire d'Hématologie, Centre de Référence des Pathologies Plaquettaires, Centre Hospitalier Universitaire de Toulouse Rangueil, F-31432 Toulouse Cedex, France.
Biomolecules. 2023 Mar 24;13(4):583. doi: 10.3390/biom13040583.
Phosphoinositides (PIs) play a crucial role in regulating intracellular signaling, actin cytoskeleton rearrangements, and membrane trafficking by binding to specific domains of effector proteins. They are primarily found in the membrane leaflets facing the cytosol. Our study demonstrates the presence of a pool of phosphatidylinositol 3-monophosphate (PI3P) in the outer leaflet of the plasma membrane of resting human and mouse platelets. This pool of PI3P is accessible to exogenous recombinant myotubularin 3-phosphatase and ABH phospholipase. Mouse platelets with loss of function of class III PI 3-kinase and class II PI 3-kinase α have a decreased level of external PI3P, suggesting a contribution of these kinases to this pool of PI3P. After injection in mouse, or incubation ex vivo in human blood, PI3P-binding proteins decorated the platelet surface as well as α-granules. Upon activation, these platelets were able to secrete the PI3P-binding proteins. These data sheds light on a previously unknown external pool of PI3P in the platelet plasma membrane that recognizes PI3P-binding proteins, leading to their uptake towards α-granules. This study raises questions about the potential function of this external PI3P in the communication of platelets with the extracellular environment, and its possible role in eliminating proteins from the plasma.
磷脂酰肌醇(PIs)通过与效应蛋白的特定结构域结合,在调节细胞内信号转导、肌动蛋白细胞骨架重排和膜运输方面发挥着关键作用。它们主要存在于面向细胞质的膜小叶中。我们的研究表明,在静息的人和鼠血小板的质膜外层小叶中存在磷酸肌醇 3-单磷酸(PI3P)的储备池。该 PI3P 储备池可被外源性重组肌管素 3-磷酸酶和 ABH 磷脂酶接触。缺失功能的 III 类 PI3-激酶和 II 类 PI3-激酶α的鼠血小板中外部 PI3P 水平降低,表明这些激酶对该 PI3P 储备池有贡献。在小鼠中注射或在人血中体外孵育后,PI3P 结合蛋白装饰血小板表面和α-颗粒。激活后,这些血小板能够分泌 PI3P 结合蛋白。这些数据揭示了血小板质膜中以前未知的外部 PI3P 储备池,该储备池识别 PI3P 结合蛋白,导致它们向α-颗粒摄取。这项研究提出了关于血小板与细胞外环境进行通讯的这个外部 PI3P 的潜在功能的问题,以及它在从血浆中消除蛋白质方面的可能作用。