聚腺苷核糖(adp -核糖)在氧化应激中发出信号

L. Virág
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引用次数: 0

摘要

聚adp核糖基化是一种依赖于nadd的蛋白质修饰反应。在各种与氧化应激相关的范式中,DNA断裂激活聚(adp -核糖)聚合酶(PARP)酶,PARP酶反过来用nadd衍生的(adp -核糖)n聚合物修饰靶蛋白。这种可逆的蛋白质修饰(PARylation)调节转录,激酶级联,代谢,分化,自噬,细胞死亡,仅举几例细胞功能和命运。此外,它还导致多种生物学结果,对糖尿病、炎症、缺血再灌注损伤和癌症等多种疾病具有广泛的影响。导致晚期糖基化终产物(AGEs)形成的途径以及AGEs的细胞效应伴随着活性氧和活性氮的过量产生,因此可能与paryl相关的病理交织在一起。讲座旨在强调氧化应激诱导的PARylation事件与age相关病理之间已证实的和可能的相互作用。
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POLY(ADP-RIBOSE) SIGNALISE IN OXIDATIVE STRESS
Poly-ADP-ribosylation is an NAD-dependent protein modification reaction. In various oxidative stress-related paradigms DNA breaks activate poly(ADP-ribose) polymerase (PARP) enzymes which in turn modify target proteins with NAD-derived (ADP-ribose)n polymers. This reversible protein modification (PARylation) regulates transcription, kinase cascades, metabolism, differentiation, autophagy, cell death only to name a few cell functions and fates. Moreover, it leads to diverse biological outcomes with wide ranging implications for diseases as diverse as diabetes, inflammation, ischemia-reperfusion injury and cancer. Pathways leading to the formation of advanced glycation endproducts (AGEs) as well as cellular effects of AGEs are accompanied by overproduction of reactive oxygen and nitrogen species and as such may be intertwined with PARylation-related pathologies. The lecture aims to highlight proven and possible interactions between the oxidative stress-induced PARylation events and AGE-related pathologies.
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