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蛋白酶体抑制剂PS-341 诱导U266 细胞凋亡与胞浆内[Ca 2+]变化的关系[J]. 肿瘤防治研究, 2007, 34(11): 822-824. DOI: 10.3971/j.issn.1000-8578.896
引用本文: 蛋白酶体抑制剂PS-341 诱导U266 细胞凋亡与胞浆内[Ca 2+]变化的关系[J]. 肿瘤防治研究, 2007, 34(11): 822-824. DOI: 10.3971/j.issn.1000-8578.896
Relationship of Proteasome Inhibitor PS-341 Induced Apoptosis with Cytoplasmic [ Ca2+]2+] ]Changes in U266 Cells[J]. Cancer Research on Prevention and Treatment, 2007, 34(11): 822-824. DOI: 10.3971/j.issn.1000-8578.896
Citation: Relationship of Proteasome Inhibitor PS-341 Induced Apoptosis with Cytoplasmic [ Ca2+]2+] ]Changes in U266 Cells[J]. Cancer Research on Prevention and Treatment, 2007, 34(11): 822-824. DOI: 10.3971/j.issn.1000-8578.896

蛋白酶体抑制剂PS-341 诱导U266 细胞凋亡与胞浆内Ca 2+变化的关系

Relationship of Proteasome Inhibitor PS-341 Induced Apoptosis with Cytoplasmic Ca2+2+ Changes in U266 Cells

  • 摘要: 目的 探讨蛋白酶体抑制剂PS-341(Bortezomib)诱导骨髓瘤细胞株U266细胞凋亡时对其胞浆内Ca2+(Ca2+i)的影响。方法 以浓度梯度的PS-341干预U266细胞4h后收集,荧光显微镜观察细胞凋亡,Annexin V-FITC/PI双参数流式细胞术(FCM)检测细胞凋亡,Fluo-3/AM荧光素标记FCM检测Ca2+i。结果 (1)PS-341作用U266细胞4h后荧光显微镜观察到凋亡细胞数随浓度增加而增多;(2)FCM检测凋亡细胞的比例分别为0.56%、7.71%、19.84%、31.10%、40.72%,与PS-341浓度成正比;(3)PS-341作用后U266细胞Ca2+i均值分别为403.65nmol/L、418.20nmol/L、378.65nmol/L、356.36nmol/L、349.21nmol/L;(4)PS-341诱导U266细胞凋亡时伴随Ca2+i的改变,浓度〉50nmol/L时诱导的细胞凋亡伴随Ca2+i下降。结论 蛋白酶体抑制荆PS-341诱导骨髓瘤细胞凋亡呈浓度依赖性;PS-341浓度〉50nmol/L时下调Ca2+i,并由此发挥抗骨髓瘤细胞作用。

     

    Abstract: Objective  To investigate the influence of proteasome inhibitor PS-341 (Bortezomib) on apoptosis-induced cell line U266 cytoplasmic Ca2+ ( Ca2+i) . Methods  U266 cells were exposed to different concent rations of PS-341 for 4 hours, then cells apoptosis were analyzed by fluorescence microscope and flow cytomet ry ( FCM) with Annexin V-FITC/ PI double staining, and cytoplasmic free calcium were detected on FCM throught Fluo-3/ AM loading. Results  (1) Apoptotic cells were gradually increased with PS-341 concentrantions increased under fluorescence microscope ; (2) The appearance rates of apoptotic cells were 0. 56 %、7. 71 %、19. 84 %、31. 10 %、40. 72 % respectively on FCM and apoptotic cells rates were in dose-dependent ; (3) The mean of Ca2+ i were 403. 65 nmol/ L 、418. 20 nmol/ L 、378. 65 nmol/ L 、356. 36 nmol/ L 、349. 21 nmol/ L, respectively, treated with PS-341. (4) PS-341 induced U266 cells apoptosis following Ca2+i change, and was related to the down regulation of Ca2+i when the dose exceeded 50nmol/ L. Conclusion  PS-341 induced U266 cells apoptosis in dose-dependent fashion ;when concentration excessed 50 nmol/ L PS-341 down regulated Ca2+i, and to exert its induce apoptosis activity by these pathways.

     

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