此研究為探討IUdR與X-ray照射,對SH-SY5Y細胞產生之影響。本實驗使用合成之放射性碘去氧尿嘧啶131IUdR,檢測SH-SY5Y細胞之吞噬率,並以SH-SY5Y細胞作為神經元模型,使用IUdR 做為輻射增敏劑再照射X-ray,並測試不同條件對細胞所造成的影響。細胞實驗選定添加使用劑量為100 µM 的IUdR與X-ray照射 2 Gy,來做為探討氧化作用對細胞產生的影響劑量,藉由MDA濃度檢測與ROS氧化檢測,來探討氧化影響對細胞蛋白質的變化。實驗結果顯示,細胞添加 IUdR或照射X-ray,確實會造成MDA與ROS濃度明顯上升,再比較X-ray照射組與IUdR+X-ray組,可發現兩組的MDA濃度相近,但針對ROS濃度所做實驗,可測得IUdR+X-ray組之ROS濃度明顯高於X-ray照射組。因此添加IUdR與照射X-ray會促進ROS濃度上升及相對提高MDA濃度,並利用以上研究結論推測ROS或可活化MAPK、PI3K/Akt等路徑來刺激細胞分裂的訊息傳遞,因而促進SH-SY5Y細胞增生。期望本研究之結論可為未來神經退化疾病等研究提供參考之依據。
This paper was indicated the effects of IUdR and X-ray to SH-SY5Y cells. This experiment was utilized radioactive 131IUdR to measure the cell uptake rate. The IUdR was used as the radiosensitizer and following the exposure of X-ray. After treated with 100 µM of IUdR and 2 Gy of X-ray, the concentrations of MDA and ROS oxidation were measured by ELISA and Chemiluminescence detection method. The experimental results showed that the IUdR and X-ray were increased MDA and ROS concentrations significantly. In conclusion, the IUdR and X-ray will encourage ROS concentration and relative MDA concentration. The ROS may induce the activation of MAPK and PI3K/Akt pathways to enhance cell division. It may provide the references for future research in neurodegenerative disease.