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本文引用的文献

1
Piezo1 and Its Function in Different Blood Cell Lineages.Piezo1 及其在不同血细胞谱系中的功能。
Cells. 2024 Mar 9;13(6):482. doi: 10.3390/cells13060482.
2
Platelet Mechanotransduction: Regulatory Cross Talk Between Mechanosensitive Receptors and Calcium Channels.血小板机械转导:机械敏感受体和钙通道之间的调节串扰。
Arterioscler Thromb Vasc Biol. 2023 Aug;43(8):1339-1348. doi: 10.1161/ATVBAHA.123.318341. Epub 2023 Jun 22.
3
Why platelet mechanotransduction matters for hemostasis and thrombosis.血小板机械转导在止血和血栓形成中的作用。
J Thromb Haemost. 2023 Sep;21(9):2339-2353. doi: 10.1016/j.jtha.2023.06.010. Epub 2023 Jun 16.
4
Activation of Piezo1 channels in compressed red blood cells augments platelet-driven contraction of blood clots.压缩红细胞中 Piezo1 通道的激活增强了血小板驱动的血栓收缩。
J Thromb Haemost. 2023 Sep;21(9):2418-2429. doi: 10.1016/j.jtha.2023.05.022. Epub 2023 Jun 1.
5
Endothelial mechanobiology in atherosclerosis.动脉粥样硬化中的血管内皮力学。
Cardiovasc Res. 2023 Jul 6;119(8):1656-1675. doi: 10.1093/cvr/cvad076.
6
Structure, signal transduction, activation, and inhibition of integrin αIIbβ3.整合素αIIbβ3的结构、信号转导、激活与抑制
Thromb J. 2023 Feb 13;21(1):18. doi: 10.1186/s12959-023-00463-w.
7
Membrane curvature governs the distribution of Piezo1 in live cells.膜曲率控制着活细胞中 Piezo1 的分布。
Nat Commun. 2022 Dec 3;13(1):7467. doi: 10.1038/s41467-022-35034-6.
8
Platelet olfactory receptor activation limits platelet reactivity and growth of aortic aneurysms.血小板嗅觉受体的激活可限制血小板的反应性和主动脉瘤的生长。
J Clin Invest. 2022 May 2;132(9). doi: 10.1172/JCI152373.
9
TRP channel function in platelets and megakaryocytes: basic mechanisms and pathophysiological impact.TRP 通道在血小板和巨核细胞中的功能:基本机制和病理生理影响。
Pharmacol Ther. 2022 Sep;237:108164. doi: 10.1016/j.pharmthera.2022.108164. Epub 2022 Mar 3.
10
PIEZO1 mediates a mechanothrombotic pathway in diabetes.Piezo1在糖尿病中介导一种机械性血栓形成途径。
Sci Transl Med. 2022 Jan 5;14(626):eabk1707. doi: 10.1126/scitranslmed.abk1707.

生物力学血小板活化:需要新型抗血小板治疗药物的疾病。

Biomechanical platelet activation: diseases that require a new class of antiplatelet therapeutics.

作者信息

Gupta Riya, Alkhalfan Fahad, Wheeler Jason, Cameron Scott J

机构信息

Section of Vascular Medicine, Department of Cardiovascular Medicine, Heart, Vascular and Thoracic Institute, Cleveland Clinic Foundation, Cleveland, Ohio, United States.

Department of Cardiovascular and Metabolic Sciences, Cleveland Clinic Lerner Research Institute of Case Western Reserve University, Cleveland, Ohio, United States.

出版信息

Am J Physiol Cell Physiol. 2025 Jun 1;328(6):C1831-C1836. doi: 10.1152/ajpcell.00228.2025. Epub 2025 Apr 24.

DOI:10.1152/ajpcell.00228.2025
PMID:40272865
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12243103/
Abstract

Mechanisms of platelet activation have traditionally been investigated through the activation of biochemical pathways through cell surface agonists such as adenosine diphosphate, thrombin, and collagen. However, recent research has identified another crucial mechanism, biomechanical activation, where external physical forces directly influence platelet reactivity. This paradigm shift underscores the complex interplay between biochemical and biomechanical stimuli in platelet activation. This review aims to understand the molecular mechanisms underlying biomechanical activation and the implications for treating thrombotic disorders.

摘要

传统上,血小板活化机制是通过细胞表面激动剂(如二磷酸腺苷、凝血酶和胶原蛋白)激活生化途径来研究的。然而,最近的研究发现了另一种关键机制,即生物力学活化,外部物理力直接影响血小板反应性。这种范式转变突显了血小板活化过程中生化和生物力学刺激之间复杂的相互作用。本综述旨在了解生物力学活化背后的分子机制及其对治疗血栓性疾病的意义。