首页> 外文期刊>The Tohoku Journal of Experimental Medicine >Lipid messenger, diacylglycerol, and its regulator, diacylglycerol kinase, in cells, organs, and animals: history and perspective.
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Lipid messenger, diacylglycerol, and its regulator, diacylglycerol kinase, in cells, organs, and animals: history and perspective.

机译:细胞,器官和动物中的脂质信使,二酰基甘油及其调节剂二酰基甘油激酶:历史和观点。

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摘要

Diacylglycerol kinase (DGK) metabolizes diacylglycerol (DG), a glycerolipid containing two acyl chains, to convert phosphatidic acid. DG is produced through phosphoinositide turnover within the membrane and is well known to act as a second messenger that modulates the activity of protein kinase C in the cellular signal transduction. Recent studies have revealed that DG also activates several proteins, including Ras guanine-nucleotide releasing protein and ion channels such as transient receptor potential proteins. Therefore, DGK is thought to participate in a number of signaling cascades by modulating levels of DG. Previous studies have disclosed that DGK is composed of a family of the isozymes, which differ in the structure, enzymological property, gene expression and localization, subcellular localization, and binding molecules. The present review focuses on the stories of phosphoinositide turnover and DG, including historical views, structural features, metabolism, and relevant cellular phenomena, together with the characteristics of DGK isozymes and the pathophysiological findings on animal studies using knockout mice and models for human diseases. Now it is being revealed that the structural and functional diversity and heterogeneity of and around DGK support the proper arrangement of the complex signal transduction machinery.
机译:二酰基甘油激酶(DGK)代谢含有两个酰基链的甘油脂二酰基甘油(DG)来转化磷脂酸。 DG是通过膜内的磷酸肌醇周转产生的,众所周知,它可作为第二信使,在细胞信号转导中调节蛋白激酶C的活性。最近的研究表明,DG还可以激活几种蛋白质,包括释放鸟嘌呤核苷酸的蛋白质和离子通道,例如瞬时受体电位蛋白。因此,认为DGK通过调节DG的水平参与许多信号级联。先前的研究已揭示DGK由同工酶家族组成,这些同工酶的结构,酶学性质,基因表达和定位,亚细胞定位和结合分子不同。本综述着重介绍磷酸肌醇发生率和DG的故事,包括历史观点,结构特征,代谢和相关的细胞现象,以及DGK同工酶的特征以及使用基因敲除小鼠和人类疾病模型进行动物研究的病理生理学发现。现在发现,DGK及其周围结构和功能的多样性和异质性支持复杂信号转导机制的正确安排。

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