1 Department of Environmental and Occupational Health, University of Pittsburgh , Pittsburgh, Pennsylvania.
2 Department of Computational and Systems Biology, University of Pittsburgh , Pittsburgh, Pennsylvania.
Antioxid Redox Signal. 2018 Nov 1;29(13):1333-1358. doi: 10.1089/ars.2017.7124. Epub 2017 Oct 16.
Oxygenated polyunsaturated lipids are known to play multi-functional roles as essential signals coordinating metabolism and physiology. Among them are well-studied eicosanoids and docosanoids that are generated via phospholipase A hydrolysis of membrane phospholipids and subsequent oxygenation of free polyunsaturated fatty acids (PUFA) by cyclooxygenases and lipoxygenases. Recent Advances: There is an emerging understanding that oxygenated PUFA-phospholipids also represent a rich signaling language with yet-to-be-deciphered details of the execution machinery-oxygenating enzymes, regulators, and receptors. Both free and esterified oxygenated PUFA signals are generated in cells, and their cross-talk and inter-conversion through the de-acylation/re-acylation reactions is not sufficiently explored.
Here, we review recent data related to oxygenated phospholipids as important damage signals that trigger programmed cell death pathways to eliminate irreparably injured cells and preserve the health of multicellular environments. We discuss the mechanisms underlying the trans-membrane redistribution and generation of oxygenated cardiolipins in mitochondria by cytochrome c as pro-apoptotic signals. We also consider the role of oxygenated phosphatidylethanolamines as proximate pro-ferroptotic signals.
We highlight the importance of sequential processes of phospholipid oxygenation and signaling in disease contexts as opportunities to use their regulatory mechanisms for the identification of new therapeutic targets.
含氧多不饱和脂质作为协调代谢和生理的必需信号,具有多功能作用,这已经得到广泛的研究。其中,研究较多的是二十烷类和二十一烷类,它们是通过细胞膜磷脂的磷脂酶 A 水解和随后的环加氧酶和脂加氧酶对游离多不饱和脂肪酸(PUFA)的氧化生成的。
人们逐渐认识到,含氧多不饱和脂肪酸磷脂也代表了一种丰富的信号语言,其中执行机制——加氧酶、调节剂和受体的细节尚未被破译。游离的和酯化的含氧多不饱和脂肪酸信号都在细胞中生成,它们通过脱酰基/再酰基反应的相互作用和相互转化尚未得到充分的研究。
在这里,我们回顾了与含氧磷脂作为重要的损伤信号有关的最新数据,这些信号触发程序性细胞死亡途径以消除不可修复的受损细胞,从而维持多细胞环境的健康。我们讨论了细胞色素 c 作为促凋亡信号在线粒体中引发跨膜重新分布和生成含氧心磷脂的机制。我们还考虑了含氧磷脂乙醇胺作为直接促铁死亡信号的作用。
我们强调了在疾病背景下磷脂氧化和信号传递的顺序过程的重要性,因为这为利用其调节机制来确定新的治疗靶点提供了机会。