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首页> 外文期刊>Journal of Investigative Dermatology Symposium Proceedings >Reactive Oxygen Species in HaCaT Keratinocytes After UVB Irradiation Are Triggered by Intracellular Ca2|[plus]| Levels
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Reactive Oxygen Species in HaCaT Keratinocytes After UVB Irradiation Are Triggered by Intracellular Ca2|[plus]| Levels

机译:细胞内Ca2 | +触发UVB辐照后HaCaT角质形成细胞中的活性氧等级

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It is recognized that reactive oxygen species (ROS) are responsible for skin damage due to UVB-radiation (UVB-R). However, the triggering substance(s) for ROS generation after UVB-R is uncertain with respect to the activation of NADPH oxidase (Nox), xanthine oxidase (XOD), and respiratory chain–chain reactions in mitochondria. As a first step in identifying the trigger(s) for UVB-induced ROS generation, we examined the relationship between Ca2+ levels and ROS generation in HaCaT keratinocytes. UVB-R exposure of HaCaT keratinocytes resulted in an immediate elevation of ROS that recurred 7hours later. This was accompanied by immediately elevated intracellular Ca2+ . A Ca2+ chelating agent, BAPTA, abolished the elevation of ROS after UVB-R completely. In addition, exogenous H2O2 did not increase intracellular Ca2+ levels. This suggests that intracellular Ca2+ is the first trigger for UVB-induced ROS generation.Abbreviations: ROS, reactive oxygen species; UVB-R, UVB-radiation
机译:人们已经认识到,活性氧(ROS)会导致由于UVB辐射(UVB-R)造成的皮肤损伤。但是,对于线粒体中NADPH氧化酶(Nox),黄嘌呤氧化酶(XOD)和呼吸链反应的激活,UVB-R后产生ROS的触发物质尚不确定。作为确定UVB诱导的ROS产生的触发因素的第一步,我们检查了HaCaT角质形成细胞中Ca2 +水平与ROS产生之间的关系。 HaCaT角质形成细胞的UVB-R暴露导致7小时后复发的ROS立即升高。这伴随着立即升高的细胞内Ca 2+。 Ca2 +螯合剂BAPTA完全消除了UVB-R后ROS的升高。此外,外源H2O2不会增加细胞内Ca2 +水平。这表明细胞内Ca2 +是UVB诱导的ROS产生的第一个触发因素。 UVB-R,UVB辐射

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