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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >A novel histidine tyrosine phosphatase, TULA-2, associates with Syk and negatively regulates GPVI signaling in platelets.
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A novel histidine tyrosine phosphatase, TULA-2, associates with Syk and negatively regulates GPVI signaling in platelets.

机译:一种新型的组氨酸酪氨酸磷酸酶TULA-2与Syk缔合并负调节血小板中的GPVI信号传导。

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摘要

T-cell ubiquitin ligand-2 (TULA-2) is a recently discovered histidine tyrosine phosphatase thought to be ubiquitously expressed. In this work, we have investigated whether TULA-2 has a key role in platelet glycoprotein VI (GPVI) signaling. This study indicates that TULA-2 is expressed in human and murine platelets and is able to associate with Syk and dephosphorylate it. Ablation of TULA-2 resulted in hyperphosphorylation of Syk and its downstream effector phospholipase C-gamma2 as well as enhanced GPVI-mediated platelet functional responses. In addition, shorter bleeding times and a prothrombotic phenotype were observed in mice lacking TULA-2. We therefore propose that TULA-2 is the primary tyrosine phosphatase mediating the dephosphorylation of Syk and thus functions as a negative regulator of GPVI signaling in platelets.
机译:T细胞泛素配体2(TULA-2)是最近发现的被普遍表达的组氨酸酪氨酸磷酸酶。在这项工作中,我们调查了TULA-2在血小板糖蛋白VI(GPVI)信号传导中是否具有关键作用。这项研究表明,TULA-2在人和鼠类血小板中表达,并能够与Syk结合并使其磷酸化。 TULA-2的消融导致Syk及其下游效应磷脂酶C-γ2的过度磷酸化,以及增强的GPVI介导的血小板功能反应。另外,在缺乏TULA-2的小鼠中观察到更短的出血时间和血栓形成表型。因此,我们建议TULA-2是介导Syk去磷酸化的主要酪氨酸磷酸酶,因此可作为血小板GPVI信号转导的负调节剂。

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