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Rho GTPase 信号在血小板调节中的作用及其在抗血小板治疗中的意义。

Rho GTPase Signaling in Platelet Regulation and Implication for Antiplatelet Therapies.

机构信息

Division of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA.

Department of Pathology, University of Cincinnati Graduate School, Cincinnati, OH 45267, USA.

出版信息

Int J Mol Sci. 2023 Jan 28;24(3):2519. doi: 10.3390/ijms24032519.

Abstract

Platelets play a vital role in regulating hemostasis and thrombosis. Rho GTPases are well known as molecular switches that control various cellular functions via a balanced GTP-binding/GTP-hydrolysis cycle and signaling cascade through downstream effectors. In platelets, Rho GTPases function as critical regulators by mediating signal transduction that drives platelet activation and aggregation. Mostly by gene targeting and pharmacological inhibition approaches, Rho GTPase family members RhoA, Rac1, and Cdc42 have been shown to be indispensable in regulating the actin cytoskeleton dynamics in platelets, affecting platelet shape change, spreading, secretion, and aggregation, leading to thrombus formation. Additionally, studies of Rho GTPase function using platelets as a non-transformed model due to their anucleated nature have revealed valuable information on cell signaling principles. This review provides an updated summary of recent advances in Rho GTPase signaling in platelet regulation. We also highlight pharmacological approaches that effectively inhibited platelet activation to explore their possible development into future antiplatelet therapies.

摘要

血小板在调节止血和血栓形成中起着至关重要的作用。Rho GTPases 作为分子开关,通过平衡的 GTP 结合/GTP 水解循环和通过下游效应器的信号级联,控制着各种细胞功能,这是众所周知的。在血小板中,Rho GTPases 通过介导信号转导发挥关键调节作用,从而驱动血小板激活和聚集。通过基因靶向和药理学抑制方法,已经证明 Rho GTPase 家族成员 RhoA、Rac1 和 Cdc42 在调节血小板中肌动蛋白细胞骨架动力学方面不可或缺,影响血小板的形状变化、扩散、分泌和聚集,导致血栓形成。此外,由于血小板无核,因此使用血小板作为未转化模型研究 Rho GTPase 功能,揭示了有关细胞信号传导原则的宝贵信息。本综述提供了 Rho GTPase 信号在血小板调节中的最新进展的最新总结。我们还强调了有效抑制血小板激活的药理学方法,以探索它们在未来抗血小板治疗中的可能发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ef5/9917354/f79e826bbab5/ijms-24-02519-g001.jpg

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