河北医药
河北醫藥
하북의약
HEBEI MEDICAL JOURNAL
2015年
2期
165-169
,共5页
王卫霄%姚苗苗%吕艳茹%杜晓欣%张晓静%赵素芬
王衛霄%姚苗苗%呂豔茹%杜曉訢%張曉靜%趙素芬
왕위소%요묘묘%려염여%두효흔%장효정%조소분
灵芝孢子粉%卵巢肿瘤%增殖%凋亡%细胞周期
靈芝孢子粉%卵巢腫瘤%增殖%凋亡%細胞週期
령지포자분%란소종류%증식%조망%세포주기
Ganoderma lucidum spore powder%ovarian neoplasms%proliferation%apoptosis%cell cycle
目的:研究灵芝孢子粉对人卵巢癌OV2008细胞增殖及凋亡的影响,并探讨其作用机制。方法采用WST-1比色法及显微镜观察法研究灵芝孢子粉对OV2008细胞生长抑制作用及细胞形态的改变;流式细胞仪检测细胞周期分布情况;Hoechst-33258染色方法评估细胞凋亡并采用western blot 方法测定凋亡相关蛋白的表达。结果WST结果表明灵芝孢子粉可以抑制OV2008细胞的生长,并呈剂量和时间依赖性;流式细胞术结果提示灵芝孢子粉可使卵巢癌细胞生长阻滞于G1期。 Hoechst-33258染色结果显示灵芝孢子处理细胞后可以检测出凋亡细胞。 Western blot方法检测到凋亡抑制蛋白bcl-2、bcl-xl随灵芝孢子浓度增加而下降,而促凋亡蛋白bax及P27、casep具有抑制卵巢癌细胞生长及诱导凋亡的作用,其机制是作用于细胞周期的ase-3逐渐升高。结论灵芝孢子粉可以抑制卵巢细胞生长,使细胞生长阻滞于G1期,并可以通过上调bax、P27,下调bcl-2并活化casepase-3而发挥其作用。
目的:研究靈芝孢子粉對人卵巢癌OV2008細胞增殖及凋亡的影響,併探討其作用機製。方法採用WST-1比色法及顯微鏡觀察法研究靈芝孢子粉對OV2008細胞生長抑製作用及細胞形態的改變;流式細胞儀檢測細胞週期分佈情況;Hoechst-33258染色方法評估細胞凋亡併採用western blot 方法測定凋亡相關蛋白的錶達。結果WST結果錶明靈芝孢子粉可以抑製OV2008細胞的生長,併呈劑量和時間依賴性;流式細胞術結果提示靈芝孢子粉可使卵巢癌細胞生長阻滯于G1期。 Hoechst-33258染色結果顯示靈芝孢子處理細胞後可以檢測齣凋亡細胞。 Western blot方法檢測到凋亡抑製蛋白bcl-2、bcl-xl隨靈芝孢子濃度增加而下降,而促凋亡蛋白bax及P27、casep具有抑製卵巢癌細胞生長及誘導凋亡的作用,其機製是作用于細胞週期的ase-3逐漸升高。結論靈芝孢子粉可以抑製卵巢細胞生長,使細胞生長阻滯于G1期,併可以通過上調bax、P27,下調bcl-2併活化casepase-3而髮揮其作用。
목적:연구령지포자분대인란소암OV2008세포증식급조망적영향,병탐토기작용궤제。방법채용WST-1비색법급현미경관찰법연구령지포자분대OV2008세포생장억제작용급세포형태적개변;류식세포의검측세포주기분포정황;Hoechst-33258염색방법평고세포조망병채용western blot 방법측정조망상관단백적표체。결과WST결과표명령지포자분가이억제OV2008세포적생장,병정제량화시간의뢰성;류식세포술결과제시령지포자분가사란소암세포생장조체우G1기。 Hoechst-33258염색결과현시령지포자처리세포후가이검측출조망세포。 Western blot방법검측도조망억제단백bcl-2、bcl-xl수령지포자농도증가이하강,이촉조망단백bax급P27、casep구유억제란소암세포생장급유도조망적작용,기궤제시작용우세포주기적ase-3축점승고。결론령지포자분가이억제란소세포생장,사세포생장조체우G1기,병가이통과상조bax、P27,하조bcl-2병활화casepase-3이발휘기작용。
Objective To investigate the effect of Ganoderma lucidum spore powder ( GLSP) on cell proliferation and apoptosis of human ovarian cell line-OV 2008,and to explore its action mechanism .Methods The effects of GLSP on OV2008 cell growth and cell morphous were detected by WST-1 colorimetric technique and microscopy; cell cycle was analyzed flow cytometry;cell apoptosis was detected by Hoechst-33258 staining method;the expression of apoptosis-related proteins ( bcl-2 bax,P27,cleaved Caspase-3) were measured by Western blotting .Results The results of WST-1 assays showed that GLSP could inhibit the growth of OV2008 cells,moreover,which was time and dose dependent .The results by flow cytometry showed that GLSP could block OV2008 cell growth at G1 phase.Hoechst 33258 staining results showed that GLSP could induce cell apoptosis.Western blotting results showed that the expression levels of bcl-2, bcl-xl were decreased with the increase of concentration of GLSP,however bax,P27,Caspase-3 could inhibit the growth of ovarian cancer cells and induce cell apoptosis , and its action mechanism was that the expression levels of Casbase-3 that affected cell cycle were gradually increased . Conclusion GLSP can inhibit the growth of ovarian cancer cells , block cell growth at G1 stage, furthermore, which can develop its effects by up-regulating the expression of bax , P27, down-regulating the expression of bcl-2 and activating Caspase-3.