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P-glycoprotein is not involved in pathway of anti-Fas/Fas-induced apoptosis in KBv200 cells

机译:P-糖蛋白不参与抗Fas / Fas诱导的KBv200细胞凋亡的途径

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摘要

AIM: To verify whether P-glycoprotein (P-gp) could induce cell resistance to apoptosis by inhibiting caspase-8 and caspase-3.METHODS: Human KB cells, either drug-sensitive or with multidrug resistance (MDR) phenotype caused by overexpression of P-gp (KBv200 cells), were treated with anti-Fas (CH-11 monoclonal antibody) to induce apoptosis. Cytotoxicity was detected by MTT assay. Symptoms of cell death were assessed by morphological observation after Hoechst33258 staining, activation of caspase-8 and caspase-3 was measured by Western blotting.RESULTS: Compared with KB cells, the resistance of KBv200 cells to VCR (vincristine) was about 51-fold higher. Anti-Fas (CH-11) induced cytotoxicity and apoptosis in both sensitive KB cells and MDR phenotype KBv200 cells. The IC50 of CH-11 in KB cells was similar to that in KBv200 cells. CH-11 induced similar apoptotic rates in both KB cells and KBv200 cells, which could be classified as caspase-dependent apoptotic pathway. Verapamil (VRP) did not affect CH-11-mediated apoptosis in KBv200 cells.CONCLUSION: Expression of P-glycoprotein does not induce resistance to caspase-8 and -3 activation or anti-Fas-induced cell apoptosis.
机译:目的:验证P-糖蛋白(P-gp)是否能通过抑制caspase-8和caspase-3诱导细胞对凋亡的抵抗力。方法:人KB细胞是药物敏感性或过度表达引起的多药耐药(MDR)表型用抗Fas(CH-11单克隆抗体)处理P-gp细胞(KBv200细胞)以诱导凋亡。通过MTT测定法检测细胞毒性。 Hoechst33258染色后通过形态学观察评估细胞死亡症状,Western blotting检测caspase-8和caspase-3的活化。结果:与KB细胞相比,KBv200细胞对VCR(长春新碱)的耐药性约为51倍。更高。 Anti-Fas(CH-11)在敏感的KB细胞和MDR表型KBv200细胞中均诱导了细胞毒性和凋亡。 CH-11在KB细胞中的IC50与KBv200细胞相似。 CH-11在KB细胞和KBv200细胞中诱导相似的凋亡率,这可以归类为caspase依赖性凋亡途径。维拉帕米(VRP)不会影响CH-11-介导的KBv200细胞凋亡。结论:P糖蛋白的表达不会诱导对caspase-8和-3激活的抗性或抗Fas诱导的细胞凋亡。

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