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Effect of shear stress on platelet activation via the glycoprotein VI receptor

机译:剪应力对糖蛋白VI受体激活血小板的影响

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Cardiovascular diseases are the nation's leading cause of death. Such diseases are caused by platelet response to collagen especially in the event of vascular injury leading to thrombosis. One of the platelet receptors known to bind to the collagen ligand is glycoprotein VI (GPVI) with co-receptor Fc receptor gamma chain (FcR/spl gamma/). By stably expressing the GPVI receptor in rat basophilic leukemia cells (RBL-2H3), which abundantly express FcR/spl gamma/, but endogenously lack GPVI, studies have shown that GPVI-FcR/spl gamma/ is sufficient to confer adhesion as well as signaling responses to collagen as long as the receptor density is equivalent to that found on human platelets. While those investigations confirm that the GPVI receptor mediate binding to collagen under static conditions, they do not provide information on how the GPVI receptor interacts with collagen under dynamic conditions. In the present study we have used the GPVI-expressing RBL-2H3 cells to observe the kinetics of adhesion to collagen under hydrodynamic flow conditions in vitro using a parallel plate flow chamber coupled with video microscopy. We demonstrate that these cells do adhere to the surface at a low shear rate and do so at a greater adherent cell density than wild-type RBL-2H3 (WT-RBL) cells.
机译:心血管疾病是美国的主要死亡原因。此类疾病是由血小板对胶原蛋白的反应引起的,尤其是在血管损伤导致血栓形成的情况下。已知与胶原配体结合的血小板受体之一是糖蛋白VI(GPVI)和共受体Fc受体γ链(FcR / spl gamma /)。通过在大鼠嗜碱性粒细胞(RBL-2H3)中稳定表达GPVI受体,该细胞大量表达FcR / spl gamma /,但内源性缺乏GPVI,研究表明GPVI-FcR / spl gamma /足以赋予粘附力,并且只要受体密度与人类血小板中的密度相同,就可以发出对胶原蛋白的信号传导响应。这些研究证实了GPVI受体在静态条件下会介导与胶原蛋白的结合,但并未提供有关GPVI受体在动态条件下如何与胶原蛋白相互作用的信息。在本研究中,我们使用表达GPVI的RBL-2H3细胞通过平行板流动室和视频显微镜在体外在水力流动条件下观察胶原蛋白的粘附动力学。我们证明,这些细胞确实以低剪切速率粘附于表面,并且以比野生型RBL-2H3(WT-RBL)细胞更大的粘附细胞密度粘附于表面。

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