首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Platelet factor 4 mediates vascular smooth muscle cell injury responses.
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Platelet factor 4 mediates vascular smooth muscle cell injury responses.

机译:血小板因子4介导血管平滑肌细胞损伤反应。

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摘要

Activated platelets release many inflammatory molecules with important roles in accelerating vascular inflammation. Much is known about platelet and platelet-derived mediator interactions with endothelial cells and leukocytes, but few studies have examined the effects of platelets on components of the vascular wall. Vascular smooth muscle cells (VSMCs) undergo phenotypic changes in response to injury including the production of inflammatory molecules, cell proliferation, cell migration, and a decline in the expression of differentiation markers. In this study, we demonstrate that the platelet-derived chemokine platelet factor 4 (PF4/CXCL4) stimulates VSMC injury responses both in vitro and in vivo in a mouse carotid ligation model. PF4 drives a VSMC inflammatory phenotype including a decline in differentiation markers, increased cytokine production, and cell proliferation. We also demonstrate that PF4 effects are mediated, in part, through increased expression of the transcription factor Krüppel-like factor 4. Our data indicate an important mechanistic role for platelets and PF4 in VSMC injury responses both in vitro and in vivo.
机译:活化的血小板释放出许多炎症分子,这些分子在加速血管炎症中具有重要作用。关于血小板和血小板衍生的与内皮细胞和白细胞的介体相互作用的了解很多,但是很少有研究检查血小板对血管壁成分的影响。血管平滑肌细胞(VSMC)响应损伤而发生表型变化,包括炎性分子的产生,细胞增殖,细胞迁移以及分化标志物表达的下降。在这项研究中,我们证明了在小鼠颈动脉结扎模型中,血小板衍生的趋化因子血小板因子4(PF4 / CXCL4)在体外和体内均可刺激VSMC损伤反应。 PF4驱动VSMC炎症表型,包括分化标志物减少,细胞因子产生增加和细胞增殖。我们还证明了PF4的作用部分是通过增加转录因子Krüppel样因子4的表达来介导的。我们的数据表明,血小板和PF4在体外和体内对VSMC损伤反应中起着重要的机械作用。

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