首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Shear enhances thrombopoiesis and formation of microparticles that induce megakaryocytic differentiation of stem cells
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Shear enhances thrombopoiesis and formation of microparticles that induce megakaryocytic differentiation of stem cells

机译:剪切增强血小板生成和微粒的形成,从而诱导干细胞的巨核细胞分化

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摘要

In vivo visualization of thrombopoiesis suggests an important role for shear flow in platelet biogenesis. In vitro, shear stress was shown to accelerate proplatelet formation from mature megakaryocytes (Mks). Yet, the role of biomechanical forces on Mk biology and platelet biogenesis remains largely unexplored. In this study, we investigated the impact of shear stress on Mk maturation and formation of platelet-like particles (PLPs), pro/preplatelets (PPTs), and Mk microparticles (MkMPs), and furthermore, we explored a physiological role for MkMPs. We found that shear accelerated DNA synthesis of immature Mks in an exposure time- and shear stress level-dependent manner. Both phosphatidylserine exposure and caspase-3 activation were enhanced by shear stress. Exposure to physiological shear dramatically increased generation of PLPs/PPTs and MkMPs by upto 10.8 and 47-fold, respectively.Caspase-3 inhibitionreduced shear-induced PLP/PPT and MkMP formation. PLPs generated under shear flow displayed improved functionality as assessed by CD62P exposure and fibrinogen binding. Significantly, coculture of MkMPs with hematopoietic stemand progenitor cells promoted hematopoietic stem and progenitor cell differentiation to mature Mks synthesizing α- and dense-granules, and forming PPTs without exogenous thrombopoietin, thus identifying a novel and unexplored potential physiological role for MkMPs.
机译:血小板生成的体内可视化表明剪切流在血小板生物发生中的重要作用。在体外,显示剪切应力可加速成熟巨核细胞(Mks)的血小板形成。然而,生物力学在Mk生物学和血小板生物发生中的作用仍未得到充分探索。在这项研究中,我们调查了剪切应力对Mk成熟以及血小板样颗粒(PLP),pro / preplatelets(PPTs)和Mk微粒(MkMPs)形成的影响,此外,我们还探讨了MkMP的生理作用。我们发现,以暴露时间和剪切应力水平依赖性的方式,剪切加速了未成熟Mks的DNA合成。剪切应力增强了磷脂酰丝氨酸的暴露和caspase-3的活化。暴露于生理剪切作用下,PLP / PPT和MkMP的生成分别显着增加了10.8和47倍.Caspase-3抑制作用减少了剪切诱导的PLP / PPT和MkMP的形成。通过CD62P暴露和血纤蛋白原结合评估,在剪切流作用下产生的PLP显示出改善的功能。重要的是,MkMPs与造血干细胞和祖细胞共培养促进了造血干细胞和祖细胞分化为成熟的Mks,合成了α-和致密颗粒,并形成了没有外源性血小板生成素的PPT,从而确定了MkMPs的一种新型且尚未探索的潜在生理作用。

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