[1]文莉莉,米永杰,陈纯海,等.TRPC3参与电磁辐射致培养的海马神经元凋亡[J].陆军军医大学学报(原第三军医大学学报),2013,35(06):491-494.
 Wen Lili,Mi Yongjie,Chen Chunhai,et al.Electromagnetic irradiation-induced apoptosis in hippocampal neurons through TRPC3[J].J Amry Med Univ (J Third Mil Med Univ),2013,35(06):491-494.
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TRPC3参与电磁辐射致培养的海马神经元凋亡(/HTML )
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陆军军医大学学报(原第三军医大学学报)[ISSN:1000-5404/CN:51-1095/R]

卷:
35卷
期数:
2013年第06期
页码:
491-494
栏目:
论著
出版日期:
2013-03-30

文章信息/Info

Title:
Electromagnetic irradiation-induced apoptosis in hippocampal neurons through TRPC3
作者:
文莉莉米永杰陈纯海李茂全
成都军区峨眉疗养院医务处;成都医学院:人体解剖与组织胚胎学教研室,公共卫生系卫生学教研室;第三军医大学军事预防医学院劳动卫生学教研室
Author(s):
Wen Lili Mi Yongjie Chen Chunhai Li Maoquan
Department of Medical Administration, Emei Sanatorium of Chengdu Military Command, Emei, Sichuan Province, 614200; Department of Human Anatomy, Histology and Embryology, Department of Public Health, Chengdu Medical College, Chengdu, Sichuan Province, 610083; Department of Occupational Health, College of Military Preventive Medicine, Third Military Medical University, Chongqing, 400038, China
关键词:
电磁辐射TRPC3神经元凋亡
Keywords:
electromagnetic irradiationTRPC3neuronapoptosis
分类号:
R135.99;R338.26;R363.21
文献标志码:
A
摘要:
目的      研究电磁辐射后,瞬时受体电位通道蛋白3(transient receptor potential channel 3,TRPC3)是否参与诱导海马神经元凋亡。      方法      以65 mW/cm2电磁波辐照原代培养的新生24 h以内Wistar大鼠海马神经元20 min,以未接受电磁波辐照的神经元为对照组,将TRPC3-siRNA和对照寡核苷酸转染神经元后分别设立为辐照+TRPC3-siRNA干扰组和辐照+TRPC3假干扰组。采用实时定量RT-PCR法及蛋白质免疫印迹法检测TRPC3 mRNA和蛋白水平的表达,电磁辐射后用CCK8试剂盒比色法检测各组细胞存活率,Annexin V-FITC试剂盒染色后经流式细胞仪检测细胞凋亡,激光共聚焦显微镜观察胞内游离钙的变化。      结果      电磁辐射可明显增加神经元中TRPC3 mRNA和蛋白表达,细胞存活率为(58.8±3.6)%,凋亡率为(30.2±2.6)%,与对照组有显著差异(P<0.05);辐照+TRPC3干扰组细胞存活率为(86.3±4.1)%,凋亡率为(9.2±0.6)%,与辐照组有显著差异(P<0.05);辐射+TRPC3假干扰组与辐射组无明显差异(P>0.05)。辐照后胞内游离钙浓度显著升高,而TRPC3干扰后可以部分抑制其升高。      结论      TRPC3表达增加所介导的细胞内游离钙升高可能是电磁辐射致海马神经元凋亡的原因之一。
Abstract:
Objective      To explore whether Canonical transient receptor potential 3 (TRPC3) plays a role in the apoptosis of hippocampal neurons induced by electromagnetic irradiation.       Methods      Primarily cultured hippocampal neurons of Wistar rats were exposed to 65 mW/cm2 electromagnetic wave for 20 min. Real-time RT-PCR and Western blotting were used to detect the expression of TRPC3 at mRNA and protein levels respectively. TRPC3-siRNA or control-siRNA was transfected into the cultured neurons. The viability of the neurons was determined by CCK8 assay, and the apoptosis of neurons were measured by flow cytometry after AnnexinV-FITC staining.       Results      Electromagnetic irradiation markedly increased mRNA and protein expression of TRPC3 and [Ca2+]i in cultured hippocampal neurons. The viability of hippocampal neurons [(58.8±3.6)%] was obviously decreased and the apoptosis rate was increased [(30.2±2.6)%] when compared with the control cells (P<0.05). TRPC3-siRNA significantly increased the survival rate [(86.3±4.1)%] and decreased the apoptosis rate [(9.2±0.6)%] and partially suppressed [Ca2+]i in the irradiation-treated cells(P<0.05), and TRPC3 false-siRNA treatment did not have these effects (P>0.05).       Conclusion      The enhanced expression of TRPC3 may be involved in the apoptosis in cultured hippocampal neurons after electromagnetic irradiation.

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更新日期/Last Update: 2013-03-19