摘要
细胞反应是由多种信号分子介导的紧密调节的过程,产生的相应的生物合成系统的调制结果。同时,一氧化氮合酶(NOS)和环氧化酶(COX)系统由和管理任务相关的构成形式(如NOS1、NOS3和COX-1)和对压力和生物活性剂形成细胞反应的诱导型形式(如NOS2和COX-2)。 可以从三个层次上观察到NOS和COX通路之间复杂的相互作用。首先,在相似和不相似的刺激反应条件下,NOS和Cox系统产物可以调节诱导型形式的表达。其次,由一氧化氮调节的环氧合酶活性和前列腺素调节NOS活性在转录后会相互影响调节。一氧化氮超氧化物歧化产物过氧亚硝基阴离子能调节前列腺素合成,如COX的S-亚硝基化和前列腺素的失活。相反,前列腺素可以促进增加动力蛋白轻链(DLC)(也被称为神经元一氧化氮合酶抑制剂)与NOS1之间的联系,从而降低其活性。相互作用的第三个层面是由NOS和COX产物引起的信号转导通路的细胞内串扰,这显着有助于细胞信号的复杂性。由于COX 和 NOS信号通路的调节与多种病理相关,其复杂的解剖关系有助于更好地了解可能的治疗方法。本文讨论了NOS和COX之间的相互作用对细胞功能和信号整合的影响。
关键词: 环氧合酶、前列腺素、一氧化氮释放信号,非甾体类抗炎药、致癌、NOS系统。
Current Medicinal Chemistry
Title:Nitric Oxide Synthase and Cyclooxygenase Pathways: A Complex Interplay in Cellular Signaling
Volume: 23 Issue: 24
Author(s): Andrey Sorokin
Affiliation:
关键词: 环氧合酶、前列腺素、一氧化氮释放信号,非甾体类抗炎药、致癌、NOS系统。
摘要: The cellular reaction to external challenges is a tightly regulated process consisting of integrated processes mediated by a variety of signaling molecules, generated as a result of modulation of corresponding biosynthetic systems. Both, nitric oxide synthase (NOS) and cyclooxygenase (COX) systems, consist of constitutive forms (NOS1, NOS3 and COX-1), which are mostly involved in housekeeping tasks, and inducible forms (NOS2 and COX-2), which shape the cellular response to stress and variety of bioactive agents. The complex interplay between NOS and COX pathways can be observed at least at three levels. Firstly, products of NOS and Cox systems can mediate the regulation and the expression of inducible forms (NOS2 and COX-2) in response of similar and dissimilar stimulus. Secondly, the reciprocal modulation of cyclooxygenase activity by nitric oxide and NOS activity by prostaglandins at the posttranslational level has been shown to occur. Mechanisms by which nitric oxide can modulate prostaglandin synthesis include direct S-nitrosylation of COX and inactivation of prostaglandin I synthase by peroxynitrite, product of superoxide reaction with nitric oxide. Prostaglandins, conversely, can promote an increased association of dynein light chain (DLC) (also known as protein inhibitor of neuronal nitric oxide synthase) with NOS1, thereby reducing its activity. The third level of interplay is provided by intracellular crosstalk of signaling pathways stimulated by products of NOS and COX which contributes significantly to the complexity of cellular signaling. Since modulation of COX and NOS pathways was shown to be principally involved in a variety of pathological conditions, the dissection of their complex relationship is needed for better understanding of possible therapeutic strategies. This review focuses on implications of interplay between NOS and COX for cellular function and signal integration.
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Cite this article as:
Andrey Sorokin , Nitric Oxide Synthase and Cyclooxygenase Pathways: A Complex Interplay in Cellular Signaling, Current Medicinal Chemistry 2016; 23 (24) . https://dx.doi.org/10.2174/0929867323666160729105312
DOI https://dx.doi.org/10.2174/0929867323666160729105312 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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