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白血病相关的Rho鸟嘌呤核苷酸交换因子对RhoA的调节并不关键,但对小鼠的血小板活化和血栓形成很重要。

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

作者信息

Williams C M, Harper M T, Goggs R, Walsh T G, Offermanns S, Poole A W

机构信息

School of Physiology & Pharmacology, University of Bristol, Bristol, UK.

Max Planck Institute for Heart and Lung Research, Bad Nauheim, Germany.

出版信息

J Thromb Haemost. 2015 Nov;13(11):2102-7. doi: 10.1111/jth.13129. Epub 2015 Oct 20.

Abstract

BACKGROUND

RhoA is an important regulator of platelet responses downstream of Gα13 , yet we still know little about its regulation in platelets. Leukemia-associated Rho guanine-nucleotide exchange factor (GEF [LARG]), a RhoA GEF, 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.

METHODS AND RESULTS

Using a platelet-specific gene knockout, we show that the absence of LARG results in a marked reduction in aggregation and dense-granule secretion in response to the thromboxane mimetic U46619 and proteinase-activated receptor 4-activating peptide, AYPGKF, but not to adenosine diphosphate. 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 the absence of LARG, although basal activity was reduced, suggesting that LARG may play a housekeeper role in regulating constitutive RhoA activity.

CONCLUSIONS

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.

摘要

背景

RhoA是Gα13下游血小板反应的重要调节因子,但我们对其在血小板中的调节机制仍知之甚少。白血病相关的Rho鸟嘌呤核苷酸交换因子(GEF [LARG]),一种RhoA GEF,在血小板中高度表达,可能构成RhoA的主要上游激活剂。为此,确定LARG在血小板功能和血栓形成中的作用很重要。

方法与结果

使用血小板特异性基因敲除,我们发现LARG的缺失导致对血栓素模拟物U46619和蛋白酶激活受体4激活肽AYPGKF的反应中聚集和致密颗粒分泌显著减少,但对二磷酸腺苷的反应不受影响。在体内氯化铁血栓形成模型中,在轻度损伤条件下,这转化为一种缺陷。重要的是,尽管基础活性降低,但激动剂诱导的RhoA激活不受LARG缺失的影响,这表明LARG可能在调节组成型RhoA活性中起管家作用。

结论

LARG在体内血小板功能和血栓形成中起重要作用。然而,尽管LARG可能在调节RhoA的静息激活状态中起作用,但其在调节血小板功能中的作用可能主要通过不依赖RhoA的途径,可能通过其他Rho家族成员。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c041/4755168/ff17b09f375c/JTH-13-2102-g001.jpg

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