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1、營養(yǎng)學報2012年第34卷第4期373SOYISOFLAVONESINDUCEDAPOPTOSIS,CELLCYCLEARRESTAND[CA]ELEVAT10NINHELACELLSXIAOJun—xia,HUANGGuo—qing,CHIYu·sen,WANGShi—qing(CollegeofFoodScienceandEngineering,QingdaoAgriculturalUniversity,Qingdao266109,Chin[Abstract]ObjectiveToinvestigatethegrow
2、thinhibitionmechanismofsoyisoflavonesmixtureSI—IonHelacells.MethodAfterexposureto10,20,and40gg/mlSI—Ifor4d,HeLacellswereexaminedwithinvertedmicroscopeandtransmissionelectronmicroscope.Thecellcycledistributionwasanalyzedbyflowcytometryandintracellularcalciumions([
3、Ca]i)detectedbyconfocallaserscanningmicroscope.ResultsTheinvertedmicroscopyshowedslowercellsgrowth,andobviousmorphologicalchanges.ThetransmissionelectronmicroscopyrevealedthatSI—IinhibitedHelacellgrowthbyinducingapoptosis.Theflowcytometryshowedthatthecellcyclewas
4、arrestedinG0/G1orGjMphasedependingonSI-Iconcentrationandtheproportionsofapoptosiscellsincreasedlinearly.Confocallaserscanningmicroscopeanalysisdemonstratedasignificantincreasein[Ca]iinSI—ItreatedHeLacells.ConclusionSI·IinhibitedHeLacellgrowththroughapoptosisinduc
5、tionandcellcyclearrestandtheincreaseofintracellular[Ca]Jmightbethemechanismsofapoptosis.]ACTANUTRIMENTASINICA,2012,34(4):373—3781Keywords:soyisoflavones;Helacells;apoptosis;cellcycle;intracellularcalciumions大百丌里黃酮誘導HeLa細胞凋亡、細胞周期阻滯和[Ca2+]i濃度升.同_C_jI—肖軍霞,黃國清,遲玉森,王世
6、清(青島農(nóng)業(yè)大學食品科學與工程學院,青島266109)【摘要l目的探討大豆異黃酮sI—I抑制HeLa細胞生長機制。方法HeLa細胞經(jīng)過10,20,and40btg/ml的大豆異黃酮sI—I處理4d后,采用倒置顯微鏡和透射電鏡觀察其形態(tài)學變化,利用流式細胞儀檢測細胞周期分布,通過激光掃描共聚焦顯微鏡觀察細胞中[ca】濃度。結(jié)果倒置顯微鏡觀察到HeLa細胞數(shù)量明顯變少,細胞嚴重變形。透射電鏡觀察到HeLa細胞發(fā)生凋亡形態(tài)學變化。流式細胞儀分析發(fā)現(xiàn)HeLa細胞周期阻滯于G/G或G/M期,細胞凋亡率隨sI—I濃度的增加而上升。激
7、光掃描共聚焦顯微鏡觀察到凋亡的HeLa細胞內(nèi)[Ca】.顯著升高。結(jié)論大豆異黃酮sI—I抑制HeLa細胞生長是通過凋亡誘導作用,并且細胞周期阻滯和【ca],濃度升高可能是其誘導凋亡機制之一。[營養(yǎng)學報,2012,34(4):373—378]關鍵詞:大豆異黃酮;HeLa細胞;凋亡;細胞周期;細胞內(nèi)鈣離子中圖分類號:R151.1文獻標識碼:A文章編號:0512—7955(2012)040373—061lNTRoDUCTIoNEcompounds,ofwhich,genistein(5,7,4一trihydroxyi—Epide
8、miologicstudiesindicatethatthesoflavone)anddaidzein(7,4一dihydroxyisonavone),consum·-ptionofsoy-containingdietsisassociatedarelikelypredominantinthecancerpreven