低剂量伽玛射线照射细胞释放的ATP通过嘌呤受体激活细胞内抗氧化系统

S. Kojima, Erina Takai, Mitsutoshi Tsukimoto
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引用次数: 13

摘要

抗氧化剂可以防止辐射引起的细胞氧化损伤。我们之前报道过,用低剂量的伽马射线对小鼠进行全身照射可提高几个器官中抗氧化剂硫氧还蛋白-1 (Trx-1)的水平。此外,伽马射线照射也会使暴露的细胞释放ATP。据报道,细胞外ATP释放响应于各种刺激,通过激活嘌呤能P2受体调节细胞内抗氧化剂的表达。在这里,我们回顾了伽马辐射诱导的ATP释放与通过嘌呤能信号传导诱导细胞Trx-1之间的关系。伽玛射线照射或外源添加ATP可导致Trx-1表达增加,这些现象在外核苷酸酶存在时消失。此外,研究表明ATP产生细胞内活性氧(ROS),从而增加Trx-1的表达,作为对ROS的适应性反应。这些发现表明,伽马辐射诱导的细胞外ATP的释放可能通过嘌呤能信号传导促进ROS的产生,从而促进细胞内抗氧化剂的产生,以应对氧化应激。
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ATP Released from Low-dose Gamma Ray-irradiated Cells Activates Intracellular Antioxidant Systems via Purine Receptors
Antioxidants are known to prevent oxidative damage in cells caused by radiation. We have previously reported that whole-body irradiation with low doses of gamma rays to mice elevates the antioxidant thioredoxin-1 (Trx-1) levels in several organs. Furthermore, gamma ray irradiation also causes ATP release from the exposed cells. Extracellular ATP release in response to various stimuli has been reported to regulate the expression of intracellular antioxidants through activation of purinergic P2 receptors. Here, we review the relation between gamma-radiation-induced ATP release and the induction of cellular Trx-1 via purinergic signaling. Irradiation with gamma rays or exogenously adding ATP cause an increase in Trx-1 expression, and these phenomena disappear in the presence of an ecto-nucleotidase. Further, it is revealed that ATP generates intracellular reactive oxygen species (ROS), and thereby increases Trx-1 expression as an adaptive response to ROS. These findings suggest that gamma-radiation-induced release of extracellular ATP may contribute to the production of ROS via purinergic signaling, thereby leading to the promotion of intracellular antioxidants in response to an oxidative stress.
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