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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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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:活化血小板释放许多具有重要作用的许多炎症分子在加速血管炎症中的重要作用。关于血小板和血小板衍生的介质与内皮细胞和白细胞的相互作用是众所周知的,但很少有研究已经检查了血小板对血管壁组分的影响。血管平滑肌细胞(VSMC)对损伤的反应进行表型变化,包括产生炎症分子,细胞增殖,细胞迁移以及分化标志物表达的下降。在本研究中,我们证明血小板衍生的趋化因子血小板因子4(PF4 / CXCL4)在小鼠颈动脉连接模型中刺激体外和体内体外的VSMC损伤反应。 PF4驱动VSMC炎症表型,包括分化标志物的下降,增加细胞因子产生和细胞增殖。我们还证明了PF4效应部分地部分地通过转录因子Krüppel样因子4的表达增加。我们的数据表明血小板和PF4在体外和体内血液损伤反应中的血小板和PF4的重要机制作用。

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