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磷脂酰肌醇-3激酶γ是炎症反应和心血管稳态的关键调节因子。

PI3Kgamma is a key regulator of inflammatory responses and cardiovascular homeostasis.

作者信息

Hawkins Phillip T, Stephens Len R

机构信息

Babraham Institute, Cambridge CB22 3AT, UK.

出版信息

Science. 2007 Oct 5;318(5847):64-6. doi: 10.1126/science.1145420.

Abstract

Class I phosphoinositide 3-kinase (PI3K) signaling pathways regulate several important cellular functions, including cellular growth, division, survival, and movement. Class IB PI3K (also known as PI3Kgamma) links heterotrimeric GTP-binding protein-coupled receptors to these pathways. Activation of class IB PI3K results in the rapid synthesis of phosphatidylinositol-3,4,5-trisphosphate [PtdIns(3,4,5)P3] and its dephosphorylation product PtdIns(3,4)P2 in the plasma membrane. These two lipid messengers bind to pleckstrin homology domain-containing effectors that regulate a complex signaling web downstream of receptor activation. Characteristic features of this pathway are the regulation of protein kinases and the regulation of small guanosine triphosphatases that control cellular movement, adhesion, contraction, and secretion. Most of the ligands that activate class IB PI3K are involved in coordinating the body's response to injury and infection, and recent studies suggest that small molecule inhibitors of this enzyme may represent a novel class of anti-inflammatory therapeutic agents.

摘要

I类磷酸肌醇3-激酶(PI3K)信号通路调控多种重要的细胞功能,包括细胞生长、分裂、存活和运动。I B类PI3K(也称为PI3Kγ)将异源三聚体GTP结合蛋白偶联受体与这些通路相连。I B类PI3K的激活导致质膜中磷脂酰肌醇-3,4,5-三磷酸[PtdIns(3,4,5)P3]及其去磷酸化产物PtdIns(3,4)P2的快速合成。这两种脂质信使与含普列克底物蛋白同源结构域的效应器结合,这些效应器在受体激活下游调控复杂的信号网络。该通路的特征是对蛋白激酶的调控以及对控制细胞运动、黏附、收缩和分泌的小GTP酶的调控。大多数激活I B类PI3K的配体参与协调机体对损伤和感染的反应,最近的研究表明,这种酶的小分子抑制剂可能代表一类新型的抗炎治疗药物。

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