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磷酸肌醇:细胞信号传导中在时间和空间上的关键参与者。

Phosphoinositides: key players in cell signalling, in time and space.

作者信息

Payrastre B, Missy K, Giuriato S, Bodin S, Plantavid M, Gratacap M

机构信息

INSERM U326, Hôpital Purpan, IFR 30, 31059, Toulouse, France.

出版信息

Cell Signal. 2001 Jun;13(6):377-87. doi: 10.1016/s0898-6568(01)00158-9.

Abstract

Over the last few years, many reports have extended our knowledge of the inositol lipid metabolism and brought out some exciting information about the location, the variety and the role of phosphoinositides (PIs). Besides the so-called "canonical PI pathway" leading to the production of phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2), the precursor of the intracellular second messengers inositol 1,4,5-trisphosphate and diacylglycerol (DAG), many other metabolic pathways have been identified to produce seven different polyphosphoinositides. Several of these quantitatively minor lipid molecules appear to be specifically involved in the control of cellular events, such as the spatial and temporal organisation of key signalling pathways, the rearrangement of the actin cytoskeleton or the intracellular vesicle trafficking. This is consistent with the fact that many of the enzymes, such as kinases and phosphatases, involved in the tight control of the intracellular level of polyphosphoinositides, are regulated and/or relocated through cell surface receptors for extracellular ligands. The remarkable feature of PIs, which can be rapidly synthesised and degraded in discrete membrane domains or even subnuclear structures, places them as ideal regulators and integrators of very dynamic mechanisms of cell regulation. In this review, we will summarise recent studies on the potential location, the metabolic pathways and the role of the different PIs. Some aspects of the temporal synthesis of D3 PIs will also be discussed.

摘要

在过去几年中,许多报告扩展了我们对肌醇脂质代谢的认识,并带来了一些有关磷酸肌醇(PIs)的位置、种类和作用的令人兴奋的信息。除了导致产生磷脂酰肌醇4,5-二磷酸(PtdIns(4,5)P2)的所谓“经典PI途径”(细胞内第二信使肌醇1,4,5-三磷酸和二酰基甘油(DAG)的前体)外,还发现了许多其他代谢途径可产生七种不同的多磷酸肌醇。其中一些在数量上较少的脂质分子似乎特别参与细胞事件的控制,例如关键信号通路的时空组织、肌动蛋白细胞骨架的重排或细胞内囊泡运输。这与以下事实一致,即许多参与严格控制细胞内多磷酸肌醇水平的酶,如激酶和磷酸酶,是通过细胞表面的细胞外配体受体进行调节和/或重新定位的。磷酸肌醇的显著特点是可以在离散的膜结构域甚至亚核结构中快速合成和降解,这使它们成为细胞调节非常动态机制的理想调节者和整合者。在这篇综述中,我们将总结关于不同磷酸肌醇的潜在位置、代谢途径和作用的最新研究。还将讨论D3磷酸肌醇的时间合成的一些方面。

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