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首页> 外文期刊>Genetics and Molecular Research >Overexpression of HSP27 in cultured human aortic smooth muscular cells reduces apoptosis induced by low-frequency and low-energy ultrasound by inhibition of an intrinsic pathway
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Overexpression of HSP27 in cultured human aortic smooth muscular cells reduces apoptosis induced by low-frequency and low-energy ultrasound by inhibition of an intrinsic pathway

机译:HSP27在培养的人主动脉平滑肌细胞中的过表达通过抑制内在途径减少了低频和低能超声诱导的凋亡

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We investigated in vitro the effect of low-frequency and low-energy ultrasound (LFLEU) on apoptosis of an overexpressed HSP27 human aortic smooth muscle cell (HASMC) line. A frequency of 42.6 kHz was used in all experiments. HASMC were exposed to ultrasound and cell viability was evaluated by MTT reduction. Overexpressed HSP27-HASMC was constructed on a pcDNA3.1 vector. Apoptosis was determined 24 h after treatment by flow cytometry; gene display was evaluated with Affimax chips, and HSP27 mRNA and protein expression levels were measured by RT-PCR and Western blotting. The apoptosis rate (at 30 s) was significantly lower in HASMC transfected with HSP27 (7.14 ± 1.73%), compared with cells transfected with a mock plasmid (17.31 ± 2.72%) or a control group (14.23 ± 2.77%), indicating a protective function for apoptosis induced by LFLEU. Gene display analysis showed that caspase-9 expression in HSP27 cell lines was downregulated and caspase-3 upregulated. However, RT-PCR and Western blotting analysis indicated that both caspase-9 and caspase-3 were inhibited at both the mRNA and protein levels. We suggest that overexpressed HSP27 is capable of protecting the LFLEU from apoptosis and that the pathway for this protection is via downregulated caspase-9 and caspase-3 expression.
机译:我们体外研究了低频和低能量超声(LFLEU)对过表达的HSP27人主动脉平滑肌细胞(HASMC)细胞凋亡的影响。在所有实验中均使用42.6 kHz的频率。将HASMC暴露于超声中,并通过MTT降低评估细胞活力。在pcDNA3.1载体上构建了过表达的HSP27-HASMC。在处理后24小时通过流式细胞仪测定细胞凋亡。使用Affimax芯片评估基因展示,并通过RT-PCR和Western blotting测量HSP27 mRNA和蛋白表达水平。与用模拟质粒(17.31±2.72%)或对照组(14.23±2.77%)转染的细胞相比,经HSP27转染的HASMC中(30 s)的凋亡率显着降低(7.14±1.73%)。对LFLEU诱导的凋亡的保护作用。基因显示分析表明,HSP27细胞系中的caspase-9表达下调,而caspase-3表达上调。但是,RT-PCR和蛋白质印迹分析表明caspase-9和caspase-3在mRNA和蛋白质水平上均受到抑制。我们建议过表达的HSP27能够保护LFLEU免受凋亡,并且这种保护的途径是通过下调caspase-9和caspase-3表达。

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