Suppr超能文献

RKIP部分通过MEK/ERK/CREB途径调节暴露于微波辐射诱导的神经细胞凋亡。

RKIP Regulates Neural Cell Apoptosis Induced by Exposure to Microwave Radiation Partly Through the MEK/ERK/CREB Pathway.

作者信息

Zuo Hongyan, Lin Tao, Wang Dewen, Peng Ruiyun, Wang Shuiming, Gao Yabing, Xu Xinping, Zhao Li, Wang Shaoxia, Su Zhentao

机构信息

Department of Experimental Pathology, Beijing Institute of Radiation Medicine, 27, Taiping Road,, Haidian District, Beijing, 100850, China.

出版信息

Mol Neurobiol. 2015;51(3):1520-9. doi: 10.1007/s12035-014-8831-5. Epub 2014 Aug 10.

Abstract

In the present study, we investigated whether Raf-1 kinase inhibitory protein (RKIP) is important for neural cell apoptosis induced by microwave exposure and explored the role of MEK/ERK/CREB pathway regulated by RKIP in the apoptosis. Differentiated PC12 cells were exposed to continuous microwave radiation at 2.856 GHz for 5 min with average power density of 30 mW/cm(2). RKIP sense and anti-sense recombinant plasmids were constructed and transfected into PC12 cells, respectively. Terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick end labeling (TUNEL) staining and caspase-3 activity assay were used to detect cell apoptosis. The results showed that RKIP was downregulated after microwave exposure while the MEK/ERK/CREB signaling pathway was activated excessively. Moreover, the ratio of Bcl-2/Bax decreased, activity of caspase-3 increased, and thus apoptotic DNA fragmentation increased. RKIP overexpression significantly inhibited the phosphorylation of MEK, ERK, and CREB, while RKIP downregulation had the reverse effect. Furthermore, U0126 was found to antagonize the changes caused by RKIP downregulation after exposure to radiation. In conclusion, RKIP plays an important role in the neural cell apoptosis induced by microwave radiation, and the regulation of cell apoptosis by RKIP is partly through the MEK/ERK/CREB pathway. This suggests that RKIP may act as a key regulator of neuronal damage caused by microwave radiation.

摘要

在本研究中,我们调查了Raf-1激酶抑制蛋白(RKIP)对微波辐射诱导的神经细胞凋亡是否重要,并探讨了由RKIP调节的MEK/ERK/CREB信号通路在凋亡中的作用。将分化的PC12细胞暴露于2.856GHz的连续微波辐射下5分钟,平均功率密度为30mW/cm²。分别构建RKIP正义和反义重组质粒并转染到PC12细胞中。采用末端脱氧核苷酸转移酶(TdT)介导的dUTP缺口末端标记(TUNEL)染色和caspase-3活性测定来检测细胞凋亡。结果显示,微波暴露后RKIP表达下调,而MEK/ERK/CREB信号通路过度激活。此外,Bcl-2/Bax比值降低,caspase-3活性增加,从而凋亡DNA片段增加。RKIP过表达显著抑制MEK、ERK和CREB的磷酸化,而RKIP下调则产生相反的效果。此外,发现U0126可拮抗辐射暴露后RKIP下调所引起的变化。总之,RKIP在微波辐射诱导的神经细胞凋亡中起重要作用,并且RKIP对细胞凋亡的调节部分是通过MEK/ERK/CREB信号通路。这表明RKIP可能是微波辐射引起神经元损伤的关键调节因子。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验