The roles of pleckstrin and pleckstrin-2 in platelet biology

该提案的目标是了解pleckstrin和pleckstrin-2在血小板粘附和血小板活化中的作用。 血栓形成Pleckstrin是一种重要的PKC底物，占血小板总细胞蛋白的约1%。 它由氨基和羧基末端Pleckstrin同源（PH）结构域和一个插入DEP组成 域尽管pleckstrin最早在血小板中被描述，但其在血小板活化中的作用仍不完全 明白我们在过表达研究中发现，普列克底物蛋白一旦被PKC磷酸化， 调节由磷脂酶C和磷脂酰肌醇3产生的磷脂第二信使， 激酶，并增强整联蛋白介导的细胞骨架变化和粘附。我们还克隆了一个cDNA pleckstrin-2是一种广泛表达的蛋白质，也存在于血小板中。Pleckstrin-2不是 磷酸化，而是通过与特定的磷脂产物结合来调节， 磷脂酰肌醇3-激酶（PI 3 K）。尽管过表达研究有助于了解 为了深入了解这两种蛋白质的潜在作用，我相信对缺乏这两种酶的血小板的研究是可行的。 这对于全面了解它们对血小板生物学的贡献至关重要。因此，我们 将无效突变引入小鼠pleckstrin基因，并产生了嵌合小鼠， 目前正在培育普列克底物蛋白基因敲除动物。我们还瞄准了pleckstrin-2基因， 并且最近产生了pleckstrin-2无效突变纯合的小鼠。普列克斯特林-2 敲除的血小板对凝血酶和胶原蛋白的聚集反应受损， 颗粒分泌，并已损害固定纤维蛋白原的传播。我假设在血小板中， pleckstrin和pleckstrin-2中等磷脂第二信使，调节血小板胞吐， 与整联蛋白协同作用以诱导肌动蛋白重组和稳定的血小板粘附。基于该 假设，我提出三个具体目标。在目的1中，我们将确定血小板与血小板膜之间的分子联系。 肌动蛋白动力学和普列克底物蛋白亚型。在目标2中，通过使用几种离体和体内模型，我们将 确定pleckstrin和pleckstrin-2对稳定血小板粘附的贡献，并检验假设 这两种亚型都是血栓形成所必需的。在目标3中，我们将使用体外方法， 包括结构研究，以进一步研究两种普列克底物蛋白同种型与磷酸肌醇的结合。

The goal of this proposal is to understand the roles of pleckstrin and pleckstrin-2 in platelet adhesion and thrombosis. Pleckstrin is a prominent PKC substrate that makes up ~1% of total cellular protein in platelets. It consists of amino- and carboxy-terminal Pleckstrin Homology (PH) domains and an intervening DEP domain. Although pleckstrin was first described in platelets, its role in platelet activation is still not completely understood. We have found in overexpression studies that pleckstrin, once it was phosphorylated by PKC, regulates phospholipid second messengers generated by both phospholipase C and phosphatidylinositol 3- kinase, and enhances integrin mediated cytoskeletal changes and adhesion. We have also cloned a cDNA for pleckstrin-2, which is a widely expressed paralog that is also present in platelets. Pleckstrin-2 is not phosphorylated by PKC, but instead is regulated by binding to specific phospholipid products of phosphatidylinositol 3-kinase (PI3K). Although overexpression studies have been useful for gaining insight into the potential role of these two proteins, I believe that studies of platelets lacking these enzymes are critical for a complete understanding of their contributions to platelet biology. Consequently, we have introduced a null mutation into the murine pleckstrin gene, and have generated chimeric mice that are currently being bred to produce pleckstrin knockout animals. We have also targeted the pleckstrin-2 gene, and have recently generated mice that are homozygous for a pleckstrin-2 null mutation. Pleckstrin-2 knockout platelets have impaired aggregation in response to thrombin and collagen, have defective dense granule secretion, and have impaired the spreading of immobilized fibrinogen. I hypothesize that in platelets, pleckstrin, and pleckstrin-2 moderate phospholipid second messengers, regulate platelet exocytosis,and function in concert with integrins to induce actin reorganization and stable platelet adhesion. Based upon this hypothesis, I propose three specific aims. InAim 1,we will determine the molecular link between platelet actin dynamics and pleckstrin isoforms. In Aim 2, by using several ex vivo and in vivo models we will determine the contribution of pleckstrin and pleckstrin-2 to stable platelet adhesion, and test the hypothesis that both of these isoforms are required for thrombus formation. In Aim 3, we will use in vitro approaches, including structural studies, to further investigate phosphoinositide binding by the two pleckstrin isoforms.