Sun Grace Y, Chuang Dennis Y, Zong Yijia, Jiang Jinghua, Lee James C M, Gu Zezong, Simonyi Agnes
Biochemistry Department, University of Missouri, 117 Schweitzer Hall, Columbia, MO, 65211, USA,
Mol Neurobiol. 2014 Aug;50(1):6-14. doi: 10.1007/s12035-014-8662-4. Epub 2014 Feb 27.
Phospholipases A(2) (PLA(2)s) are important enzymes for the metabolism of fatty acids in membrane phospholipids. Among the three major classes of PLA(2)s in the mammalian system, the group IV calcium-dependent cytosolic PLA(2) alpha (cPLA(2)α) has received the most attention because it is widely expressed in nearly all mammalian cells and its active participation in cell metabolism. Besides Ca(2+) binding to its C2 domain, this enzyme can undergo a number of cell-specific post-translational modifications, including phosphorylation by protein kinases, S-nitrosylation through interaction with nitric oxide (NO), as well as interaction with other proteins and lipid molecules. Hydrolysis of phospholipids by cPLA(2) yields two important lipid mediators, arachidonic acid (AA) and lysophospholipids. While AA is known to serve as a substrate for cyclooxygenases and lipoxygenases, which are enzymes for the synthesis of eicosanoids and leukotrienes, lysophospholipids are known to possess detergent-like properties capable of altering microdomains of cell membranes. An important feature of cPLA(2) is its link to cell surface receptors that stimulate signaling pathways associated with activation of protein kinases and production of reactive oxygen species (ROS). In the central nervous system (CNS), cPLA(2) activation has been implicated in neuronal excitation, synaptic secretion, apoptosis, cell-cell interaction, cognitive and behavioral function, oxidative-nitrosative stress, and inflammatory responses that underline the pathogenesis of a number of neurodegenerative diseases. However, the types of extracellular agonists that target intracellular signaling pathways leading to cPLA(2) activation among different cell types and under different physiological and pathological conditions have not been investigated in detail. In this review, special emphasis is given to metabolic events linking cPLA(2) to activation in neurons, astrocytes, microglial cells, and cerebrovascular cells. Understanding the molecular mechanism(s) for regulation of this enzyme is deemed important in the development of new therapeutic targets for the treatment and prevention of neurodegenerative diseases.
磷脂酶A(2)(PLA(2))是膜磷脂中脂肪酸代谢的重要酶类。在哺乳动物系统的三大类PLA(2)中,IV组钙依赖性胞质磷脂酶A(2)α(cPLA(2)α)受到了最多关注,因为它在几乎所有哺乳动物细胞中广泛表达并积极参与细胞代谢。除了钙离子与它的C2结构域结合外,这种酶还能经历多种细胞特异性的翻译后修饰,包括蛋白激酶的磷酸化、通过与一氧化氮(NO)相互作用进行的S-亚硝基化,以及与其他蛋白质和脂质分子的相互作用。cPLA(2)对磷脂的水解产生两种重要的脂质介质,花生四烯酸(AA)和溶血磷脂。虽然已知AA是环氧化酶和脂氧合酶的底物,这两种酶用于合成类二十烷酸和白三烯,但已知溶血磷脂具有类似去污剂的特性,能够改变细胞膜的微结构域。cPLA(2)的一个重要特征是它与细胞表面受体的联系,这些受体刺激与蛋白激酶激活和活性氧(ROS)产生相关的信号通路。在中枢神经系统(CNS)中,cPLA(2)的激活与神经元兴奋、突触分泌、细胞凋亡、细胞间相互作用、认知和行为功能、氧化-亚硝化应激以及炎症反应有关,这些反应是许多神经退行性疾病发病机制的基础。然而,在不同细胞类型以及不同生理和病理条件下,靶向导致cPLA(2)激活的细胞内信号通路的细胞外激动剂类型尚未得到详细研究。在这篇综述中,特别强调了将cPLA(2)与神经元、星形胶质细胞、小胶质细胞和脑血管细胞中的激活联系起来的代谢事件。了解这种酶的调节分子机制被认为在开发治疗和预防神经退行性疾病的新治疗靶点方面很重要。