摘要
诱导型一氧化氮合酶(iNOS)在多种类型细胞中得到表达,尤其是在炎症细胞中,对不同的炎症包括病毒蛋白Tat和gp120有反应。这种反应发生在一氧化氮(NO)水平下降之早期之前,这取决于导致一氧化氮合酶(cNOS)本构亚型抑制作用的信号。这个过程需要Ca2+依赖的磷脂酶A2激活所产生的的花生四烯酸(AA)的临界水平,并由下游酪氨酸激酶依赖性iNOS磷酸化所调节。降低NO水平核对激活因子κB活性是必要的,从而有助于由该转录因子调控的多种基因如iNOS的表达。值得注意的是,两个小的脂溶性分子,NO和AA可以在远端细胞触发上述反应。因此,产生于炎症反应早期阶段的AA是使“NO tone”调节从生理过程(由cNOS调节)转化为病理过程(由iNOS调节)的关键因素。炎症反应的后期阶段通常伴随着组织中有害影响的发生,这是由iNOS 衍生物NO以及AA代谢产物所引起。本文讨论了在HIV相关的神经机制中NOS亚型之间的相互影响,突出没有和AA为介质的毒性作用的影响,并突出了“NO”和“AA” 作为细胞毒性介质的作用。
关键词: 花生四烯酸,星形胶质细胞,一氧化氮合酶,磷脂酶A2,一氧化氮,一方面,HIV,诱导型NOS。
Current Medicinal Chemistry
Title:Cross-Talk Between NO Synthase Isoforms in Neuro-Inflammation: Possible Implications in HIV-Associated Neurocognitive Disorders
Volume: 23 Issue: 24
Author(s): Tiziana Persichini, Sofia Mariotto, Hisanori Suzuki, Elena Butturini, Roberta Mastrantonio, Orazio Cantoni, Marco Colasanti
Affiliation:
关键词: 花生四烯酸,星形胶质细胞,一氧化氮合酶,磷脂酶A2,一氧化氮,一方面,HIV,诱导型NOS。
摘要: Inducible nitric oxide synthase (iNOS) is expressed in several cell types, particularly in inflammatory cells, in response to diverse proinflammatory stimuli, including viral proteins as HIV Tat and gp120. This response is preceded by an early decline in basal nitric oxide (NO) levels, dependent on a signaling leading to inhibition of the constitutive isoform of NO synthase (cNOS). This process requires critical levels of arachidonic acid (AA), generated by Ca2+-dependent activation of cytosolic phospholipase A2, and is mediated by the downstream tyrosine kinase-dependent phosphorylation of cNOS. Lowering basal NO levels are necessary for the activation of nuclear factor-κB, and thus for the expression of a variety of genes regulated by this transcription factor, which include iNOS. Notably, NO and AA, two small lipid soluble molecules, can trigger the above responses also in distal cells. Thus, AA produced at the very early stages of the inflammatory response is a likely critical signal switching the regulation of the “NO tone” from physiological (i.e., mediated by cNOS) to pathological (i.e., mediated by iNOS). This later phase of the inflammatory response is often accompanied by the onset of deleterious effects in the tissue, in which a critical role is played by iNOS-derived NO (directly or indirectly, i.e., via formation of peroxynitrite) as well as by products of the AA cascade. In this review, the authors discuss the implications of the crosstalk between the NOS isoforms in HIV-associated neuro-pathogenesis highlighting the role of NO and AA as mediators of cytotoxicity.
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Tiziana Persichini, Sofia Mariotto, Hisanori Suzuki, Elena Butturini, Roberta Mastrantonio, Orazio Cantoni, Marco Colasanti , Cross-Talk Between NO Synthase Isoforms in Neuro-Inflammation: Possible Implications in HIV-Associated Neurocognitive Disorders, Current Medicinal Chemistry 2016; 23 (24) . https://dx.doi.org/10.2174/0929867323666160809100452
DOI https://dx.doi.org/10.2174/0929867323666160809100452 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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