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Leukemia-associated Rho guanine-nucleotide exchange factor is not critical for RhoA regulation, yet is important for platelet activation and thrombosis in mice

机译:白血病相关的Rho鸟嘌呤核苷酸交换因子对于RhoA调节并不重要,但对小鼠的血小板活化和血栓形成却很重要

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摘要

: RhoA is an important regulator of platelet responses downstream of Gα, yet we still know little about its regulation in platelets. Leukemia-Associated RhoGEF (LAR6G), a RhoAGEF, is highly expressed in platelets and may constitute a major upstream activator of RhoA. To this end, it is important to determine the role of LARG in platelet function and thrombosis.: Using a platelet-specific gene knockout, we show that absence of LARG results in a marked reduction in aggregation and dense-granule secretion in response to the thromboxane mimetic, U46619, and PAR4-activating peptide, AYPGKF, but not to ADP. In a ferric chloride thrombosis model in vivo, this translated into a defect, under mild injury conditions. Importantly, agonist-induced RhoA activation was not affected by absence of LARG, although basal activity was reduced, suggesting that LARG may play a house-keeper role in regulating constitutive RhoA activity.LARG plays an important role in platelet function and thrombosis in vivo. However, although LARG may have a role in regulating the resting activation state of RhoA, its role in regulating platelet function may principally be through RhoA-independent pathways, possibly through other Rho-family members.
机译::RhoA是Gα下游血小板反应的重要调节剂,但我们对其在血小板中的调节知之甚少。白血病相关的RhoGEF(LAR6G),RhoAGEF,在血小板中高表达,可能构成RhoA的主要上游激活剂。为此,重要的是要确定LARG在血小板功能和血栓形成中的作用。:使用血小板特异性基因敲除,我们显示出LARG的缺乏会导致对血小板反应的聚集和致密颗粒分泌的明显减少。血栓烷模拟物U46619和PAR4激活肽AYPGKF,但不包括ADP。在体内氯化铁血栓形成模型中,在轻度损伤条件下,这转化为缺陷。重要的是,激动剂诱导的RhoA活化不受基础RGAR活性降低的影响,尽管基础活性降低,这表明LARG可能在管控RhoA组成型活性中起管家作用.LARG在体内血小板功能和血栓形成中起重要作用。但是,尽管LARG可能在调节RhoA的静止激活状态中起作用,但其在调节血小板功能中的作用可能主要是通过RhoA独立途径,也可能是通过其他Rho家族成员。

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