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X射线照射对原代培养海马神经元突起生长的作用
引用本文:何如,李骁扬,孙锐,田野.X射线照射对原代培养海马神经元突起生长的作用[J].中华放射医学与防护杂志,2015,35(8):570-574.
作者姓名:何如  李骁扬  孙锐  田野
作者单位:215004 苏州大学附属第二医院放疗科 苏州大学放射肿瘤治疗学研究所,215004 苏州大学附属第二医院放疗科 苏州大学放射肿瘤治疗学研究所,215004 苏州大学附属第二医院放疗科 苏州大学放射肿瘤治疗学研究所,215004 苏州大学附属第二医院放疗科 苏州大学放射肿瘤治疗学研究所
基金项目:国家自然科学基金(81372411,81172128);江苏省临床医学科技专项资助项目(BL2014040);江苏省研究生创新工程项目(CXZZ13_0838)
摘    要:目的 探讨X射线照射对离体培养原代海马神经元突起生长的作用。方法 采用离体的方式培养原代海马神经元,分别给予0、2、4、8、10和12 Gy剂量照射,在照射后第1天和第3天,采用MTT法检测电离辐射对原代海马神经元死亡的影响,免疫荧光染色检测电离辐射对原代海马神经元神经突起的影响。结果 在照射后第1天和第3天,随着剂量的增加,海马神经元细胞死亡增多,差异有统计学意义(F=123.068、43.370,P<0.05),但4、8、10和12 Gy照射组间差异无统计学意义(P>0.05)。不同剂量照射后第1天,神经突起长度、总树突分支长度(TDBL)差异均有统计学意义(F=9.169、7.856,P<0.05),照后第3天神经突起长度、TDBL和总树突分支点数(TDBTN)差异均有统计学意义(F=23.797、6.565、6.021,P<0.05)。结论 X射线照射对离体培养的原代海马神经元突起的生长具有抑制作用。

关 键 词:X射线  神经元  神经突起  海马  离体
收稿时间:3/6/2015 12:00:00 AM

Effect of X-ray irradiation on the neurites growth of primary hippocampal neurons
He Ru,Li Xiaoyang,Sun Rui and Tian Ye.Effect of X-ray irradiation on the neurites growth of primary hippocampal neurons[J].Chinese Journal of Radiological Medicine and Protection,2015,35(8):570-574.
Authors:He Ru  Li Xiaoyang  Sun Rui and Tian Ye
Institution:Department of Radiation Oncology, Second Affiliated Hospital of Soochow University, Suzhou 215004, China,Department of Radiation Oncology, Second Affiliated Hospital of Soochow University, Suzhou 215004, China,Department of Radiation Oncology, Second Affiliated Hospital of Soochow University, Suzhou 215004, China and Department of Radiation Oncology, Second Affiliated Hospital of Soochow University, Suzhou 215004, China
Abstract:Objective To investigate the effect of X-ray irradiation on neurites growth of primary hippocampal neurons in vitro. Methods Primary hippocampal neuron culture in vitro were irradiated with 0, 2, 4, 8, 10, 12 Gy of X-rays. In the first day and the third day after irradiation, the cell death of primary hippocampal neurons was detected by MTT method, and the morphological changes of primary hippocampal neuronal neurites were detected with immunofluorescence staining method. Results In the first day and third day after irradiation, the cell death of hippocampal neurons increased significantly (F=123.068, 43.370,P<0.05), but there were no significant difference among 4, 8, 10, and 12 Gy irradiation groups. Immunofluorescence staining showed that, in the first day after irradiation, the neurite length and total dendritic branch length (TDBL) were significantly changed (F=9.169, 7.856, P<0.05), and in the third day after radiation,the neurite length, TDBL and total dendritic branch tip number (TDBTN) were also altered (F=23.797, 6.565, 6.021, P<0.05). Conclusion X-ray irradiation can inhibit the growth of neurites in the primary hippocampal neurons in vitro.
Keywords:X-rays  Neuron  Neurite  Hippocampus  In vitro
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