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Olecular mechanism underlying the myeloperoxidase induced apoptosis of HUVEC-12 cells

机译:髓过氧化物酶诱导HUVEC-12细胞凋亡的分子机制

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Objective: This study aimed to investigate the molecular mechanism underlying the myeloperoxidase (MPO) induced apoptosis of human umbilical vein endothelial cells (HUVECs). Methods: HUVEC-12 cells were treated with myeloperoxidase at different concentrations (0.1 μ/ml, 0.2 μ/ml, 0.4 μ/ml and 0.6 μ/ml) and apoptotic cells were detected by flow cytometry. Then, cells were harvested for the detection of mRNA and protein expression of caspase-3 and Bax by reverse transcription PCR and Western blot assay, respectively. Results: When compared with negative control group, the apoptosis index in 0.2 μ/ml MPO group, 0.4 μ/ml MPO group and 0.6 μ/ml MPO group increased markedly (P<0.05). When compared with negative control group, the mRNA expression of caspase-3 in 0.6 μ/ml MPO group and positive control group increased dramatically (P<0.05). When compared with negative control group, the protein expression of pre-caspase-3 and activated caspase-3 elevated significantly in 0.4 μ/ml MPO group, 0.6 μ/ml MPO group and positive control group (P<0.05). When compared with negative control group, the mRNA and protein expression of Bax elevated dramatically in 0.4 μ/ml MPO group, 0.6 μ/ml MPO group and positive control group (P<0.05). Conclusion: MPO at certain extents may induce the apoptosis of HUVEC-12. The MPO induced apoptosis of HUVEC-12 may be dependent on capase-3 signaling pathway, and Bax is also involved in the MPO induced apoptosis of HUVEC-12.
机译:目的:本研究旨在探讨髓过氧化物酶(MPO)诱导人脐静脉内皮细胞(HUVEC)凋亡的分子机制。方法:用不同浓度的髓过氧化物酶处理HUVEC-12细胞(0.1和0.1、0.2和0.4、0.6和0.6)。通过流式细胞仪检测。然后,收集细胞,分别通过逆转录PCR和蛋白质印迹法检测caspase-3和Bax的mRNA和蛋白表达。结果:与阴性对照组相比,细胞凋亡指数在0.2& MMP组,0.4&#x003b / ml MPO组和0.6&#x003bc / ml MPO组中显着增加(P< 0.05)。 )。与阴性对照组相比,MPA组和阳性对照组的caspase-3 mRNA表达在0.6和/ ml显着增加(P< 0.05)。与阴性对照组相比,MPA组在0.4& MPO组和阳性对照组在0.6&#x003bc / ml的前半胱天冬酶3和活化的caspase-3的蛋白表达显着升高(P&# x0003c; 0.05)。与阴性对照组相比,Bax的mRNA和蛋白表达在0.4和/ ml MPO组,0.6和/ ml MPO组和阳性对照组中显着升高(P< 0.05)。结论:MPO在一定程度上可诱导HUVEC-12凋亡。 MPO诱导的HUVEC-12凋亡可能依赖于capase-3信号通路,Bax也参与MPO诱导的HUVEC-12凋亡。

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