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首页> 外文期刊>Artificial cells, nanomedicine, and biotechnology. >PLCG2 promotes hepatocyte proliferation in vitro via NF-κB and ERK pathway by targeting bcl2 , myc and ccnd1
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PLCG2 promotes hepatocyte proliferation in vitro via NF-κB and ERK pathway by targeting bcl2 , myc and ccnd1

机译:PLCG2通过靶向bcl2,myc和ccnd1通过NF-κB和ERK途径体外促进肝细胞增殖

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摘要

Phospholipase Cγ2 (PLCG2) has been implicated in the regulation of cell proliferation, transformation, and tumor growth. In this study, we investigate the mechanism of PLCG2 action using a short interference RNA (siRNA) method. The effects of PLCG2 on rat liver BRL-3A cells treated siRNA were studied by 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide (MTT assay), bromodeoxyuridine (BrdU) labelling assay, flow cytometry method (FCM), quantitative real-time polymerase chain reaction (qRT-PCR) and western blot. The results showed when PLCG2 was reduced, cell vitality and proliferation rate were significantly decreased ( p ?.05 vs. control). FCM analysis showed that the number of cell division phase (G2?+?M) was declined ( p ?.05 vs. control). RT-PCR and western blot revealed that the expression of signalling related genes NF-κB, FOS, JUN and ELK, target genes BCL2, CCNB1 and CCND1 were remarkably down-regulated in cells treated with PLCG2 siRNAs. Based on these results, we conclude PLCG2 plays an important role in rat liver cell proliferation via ERK and NF-κB pathway by regulating the expression of BCl2, MYC and CCND1 .
机译:磷脂酶Cγ2(PLCG2)已参与细胞增殖,转化和肿瘤生长的调控。在这项研究中,我们使用短干扰RNA(siRNA)方法研究PLCG2作用的机制。用3-(4,5-二甲基-2-噻唑基)-2,5-二苯基-2-H-溴化四氮唑(MTT法),溴脱氧尿苷(BrdU)研究PLCG2对大鼠肝BRL-3A细胞处理的siRNA的影响)标记测定,流式细胞仪方法(FCM),定量实时聚合酶链反应(qRT-PCR)和Western印迹。结果显示,当PLCG2减少时,细胞活力和增殖速率显着降低(与对照组相比,p <?0.05)。 FCM分析表明细胞分裂期(G2β+ΔM)的数目减少了(与对照相比,p <Δ0.05)。 RT-PCR和western blot分析显示,PLCG2 siRNA处理后的细胞中信号相关基因NF-κB,FOS,JUN和ELK,靶基因BCL2,CCNB1和CCND1的表达明显下调。根据这些结果,我们得出结论,PLCG2通过调节BCl2,MYC和CCND1的表达,通过ERK和NF-κB途径在大鼠肝细胞增殖中起重要作用。

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