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亚低温上调Sirt1减少氧糖剥夺后原代神经元细胞凋亡 被引量:1

Mild hypothermia reduces neurons apoptosis after OGD by up-regulating Sirt1
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摘要 为探讨亚低温对氧糖剥夺/复氧后原代神经元细胞自噬和凋亡的影响,运用原代神经元培养及OGD/R模型构建,CCK8测定细胞活力,TUNEL检测细胞凋亡,Western-blot检测Sirt1、Foxo1、Rab7、Beclin1、LC3及p53等蛋白的表达,以及转染mRFP-GFP-LC3自噬双标腺病毒检测神经元自噬流等方法,成功培养原代神经元及构建OGD/R模型。结果发现OGD/R后Sirt1、P-Foxo1、Rab7、Beclin1、LC3b/LC3a表达随着时间延长逐渐减少,12 h更明显,与R6 h组相比,P<0.05,而p53增加,P<0.05;OGD3 h/R12 h,亚低温组Sirt1、P-Foxo1、Rab7、Beclin1及LC3b/LC3a表达均明显高于常温组,P<0.05,而p53明显低于常温组,P<0.05。R6 h亚低温组,神经元凋亡率为20%±6.7%,低于常温组的56.8%±7.6%,P<0.05。mRFP-GFP-LC3自噬双标观察法显示亚低温组自噬溶酶体明显增多,P<0.05。实验显示原代神经元OGD/R后亚低温干预可以上调Sirt1的活性,增加Foxo1、Rab7和自噬相关蛋白Beclin1、LC3b/LC3a的表达,同时抑制p53,促进神经元自噬,减少凋亡。 To investigate the primary neurons autophagy and apoptosis after Oxygen Glucose Deprivation/Re oxygenation(OGD/R),and to explore the effect of mild hypothermia on autophagy and apoptosis,following methods were used:Primary neurons culture and OGD/R model was established;the neurons were divided into the normal temperature group(37℃)and the mild hypothermia group(MH,34℃);The cells viability were measured by CCK8;cell apoptosis were measured by TUNEL;The protein expressions of Sirt1,Foxo1,p53,Rab7and autophagy related genes such as Beclin1,LC3were detected by western blot at each time point;The neurons autophagy flows were detected through transfection of adenovirus mRFP GFP LC3.The primary neuron cultures were successfully developed,and the OGD/R models were established;Western blot showed that the expressions of Sirt1,P Foxo1,Rab7,Beclin1and LC3b/LC3a were gradually reduced,especially at12h after OGD/R,P<005;However,the expression of p53was increased,P<005;In MH group,the expressions of Sirt1,P Foxo1,Rab7,Beclin1,LC3b/LC3a were obviously higher than those in NT group,P<005;And the expression of p53was obviously lower than that in NT group,P<005;in R6h+MH group,the rate of neuron cells apoptosis were20%±67%,lower than568%±76%in R6h+NT group,P<005;mRFP GFP LC3adenovirus was transfected into primary neurons,the autophagy flow was detected by fluorescence microscopy.Compared with control group,the autolysosomes were reduced,but autophagosomes were increased after OGD/R,P<005;however,compared with NT group,the autophagosomes were reduced and the autolysosomes were increased in MH group,P<005.In conclusion,mild hypothermia therapy could increase the expression of Sirt1,Foxo1,beclin1and LC3b/LC3a,but decrease the expression of p53,so as to promote autophagy and reduce apoptosis.
作者 尹美娴 胡春林 魏红艳 廖晓星 李恒杰 杨焰 李慧 荆小莉 李浩明 YIN Meixian;HU Chunlin;WEI Hongyan;LIAO Xiaoxing;LI Hengjie;YANG Yan;LI Hui;JING Xiaoli;LI Haoming(School of Life Science and Biopharmacology, Guangdong Parmaceutical University, Guangzhou 510006, China;Department of Emergency Medicine, the First Affiliated Hospital of Sun Yat sen University, Guangzhou 510080, China;Key Laboratory of Assisted Circulation, Ministry of Health, Guangzhou 510080, China)
出处 《中山大学学报(自然科学版)》 CAS CSCD 北大核心 2017年第6期134-140,共7页 Acta Scientiarum Naturalium Universitatis Sunyatseni
基金 国家自然科学基金(81372021 81571867) 第四批中山一院青年人才项目(Y50152)
关键词 亚低温 SIRT1 神经元细胞 mild hypothermia Sirt1 neurons
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