丁敬宾, 王志军, 司胜斌, 丁娟, 赵薇. 新制癌菌素诱导小鼠海马神经元细胞DNA损伤的作用研究*[J]. 云南大学学报(自然科学版), 2018, 40(3): 603-608. doi: 10.7540/j.ynu.20170689
引用本文: 丁敬宾, 王志军, 司胜斌, 丁娟, 赵薇. 新制癌菌素诱导小鼠海马神经元细胞DNA损伤的作用研究*[J]. 云南大学学报(自然科学版), 2018, 40(3): 603-608. doi: 10.7540/j.ynu.20170689
DING Jing-bin, WANG Zhi-jun, SI Sheng-bin, DING Juan, ZHAO Wei. Effects of NCS on DNA damage in HT22 of mouse[J]. Journal of Yunnan University: Natural Sciences Edition, 2018, 40(3): 603-608. DOI: 10.7540/j.ynu.20170689
Citation: DING Jing-bin, WANG Zhi-jun, SI Sheng-bin, DING Juan, ZHAO Wei. Effects of NCS on DNA damage in HT22 of mouse[J]. Journal of Yunnan University: Natural Sciences Edition, 2018, 40(3): 603-608. DOI: 10.7540/j.ynu.20170689

新制癌菌素诱导小鼠海马神经元细胞DNA损伤的作用研究*

Effects of NCS on DNA damage in HT22 of mouse

  • 摘要: 为了探索化学诱导物新制癌菌素(NCS)对小鼠海马神经元细胞株HT22 DNA损伤的影响,研究以9Gy X射线辐照为阳性对照组,通过CCK8试剂盒法检测绘制NCS作用下HT22细胞生长曲线以明确NCS处理细胞的最佳浓度,经Hoechst染色和TUNEL染色观察该剂量NCS对细胞DNA损伤及凋亡的影响,用免疫荧光染色结合Western blot分析HT22细胞核中DNA损伤反应酶PARP1的表达变化.结果显示,NCS作用的终质量浓度为1000ng/mL时,从48h起对HT22细胞增殖表现出显著的抑制作用;Hoechst染色可见NCS作用下HT22细胞DNA损伤加剧,TUNEL染色提示NCS能够诱导细胞凋亡;免疫荧光染色和Western-blot实验显示NCS能够促进细胞核内PARP1的表达.说明化学诱导剂NCS能够引起HT22细胞DNA损伤及凋亡以及上调DNA损伤反应酶PARP1的表达,可以用于模拟大剂量射线对细胞的辐射损伤效应.

     

    Abstract: To explore the effect of chemical inducer neocarzinostatin (NCS) on the DNA damage of mouse hippocampal neuron cell line HT22,9 Gy X-ray irradiation was used as a positive control group.The growth curve of HT22 cells after NCS treatment were detected by CCK8 kit method to verify the optimal concentration of NCS in treating cells in this study.Hoechst staining and TUNEL staining were used to investigate the effects of NCS at optimal concentration on the cellular DNA damage and apoptosis. Immunofluorescence staining and Western blot were used to analyze the expression changes of PARP1-DNA damage reaction enzyme in HT22 cell nuclei.The results showed that when the concentration of NCS was 1000ng/mL,the proliferation of HT22 cells were significantly inhibited from 48h;Hoechst staining showed that DNA damage of HT22 cells were exacerbated by NCS.TUNEL staining suggested that NCS can induce cellular apoptosis.Immunofluorescence staining and Western blot showed that NCS can promote the expression of PARP1 in the nucleus.The results indicated that chemical inducer NCS can induce DNA damage and apoptosis in HT22 cells and up-regulate the expression of PARP1. It can be used to simulate the radiation damage effect of high dose radiation on cells.

     

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