koko体育app

欢迎来到《koko体育app 学报(医学版)》
胡秀秀, 刘北忠, 钟梁等. Ad-NLS-RARα对HL-60细胞增殖及ATRA诱导的HL-60细胞分化的影响及其机制[J]. koko体育app 学报(医学版), 2013, 44(6): 897-901.
引用本文: 胡秀秀, 刘北忠, 钟梁等. Ad-NLS-RARα对HL-60肿瘤血细胞增值能力及ATRA诱骗的HL-60肿瘤血细胞两极分化的作用简述管理机制[J]. 江西学校学报(临床医学版), 2013, 44(6): 897-901.
HU Xiu-xiu, LIU Bei-zhong, ZHONG Liang. et al. Effect of Recombinant Adenovirus Carrying NLS-RARα Gene on the Proliferation of HL-60 Cell and the[J]. Journal of Sichuan University (Medical Sciences), 2013, 44(6): 897-901.
Citation: HU Xiu-xiu, LIU Bei-zhong, ZHONG Liang. et al. Effect of Recombinant Adenovirus Carrying NLS-RARα Gene on the Proliferation of HL-60 Cell and the[J]. Journal of Sichuan University (Medical Sciences), 2013, 44(6): 897-901.

Ad-NLS-RARα对HL-60细胞增殖及ATRA诱导的HL-60细胞分化的影响及其机制

Effect of Recombinant Adenovirus Carrying NLS-RARα Gene on the Proliferation of HL-60 Cell and the

  • 摘要: 目的 将已构建验证成功的重组腺病毒Ad-NLS-RARα感染至HL-60细胞中,探讨其对HL-60细胞增殖及全反式维甲酸(ATRA)诱导的HL-60细胞分化的影响及机制。方法 将验证正确的腺病毒经Protamine sulfate辅助感染HL-60细胞,检测感染效率,用RT-PCR和Western blot检测目的基因在HL-60细胞中的表达情况。MTT法检测细胞增殖情况。病毒感染HL-60细胞24 h后,用2.5 μmol/L ATRA处理,流式细胞术(FCM)检测细胞表面分化抗原CD11b的表达。RT-PCR和Western blot检测C-MYC基因在mRNA和蛋白水平的表达。结果 在Protamine sulfate辅助感染作用下,重组腺病毒Ad-NLS-RARα和阴性对照腺病毒Ad-KZ对HL-60细胞的感染效率可达70%~80%。NLS-RARα基因的RT-PCR和Western blot结果显示,感染了重组腺病毒Ad-NLS-RARα的HL-60细胞的NLS-RARα基因的mRNA及蛋白表达水平明显增高(P<0.05)。MTT法检测表明感染了重组腺病毒Ad-NLS-RARα的细胞增殖能力增高 (P<0.05)。FCM检测结果显示,经ATRA处理后,感染Ad-NLS-RARα重组腺病毒的HL-60细胞,CD11b表达较阴性对照组和未感染组下调(P<0.05)。C-MYC基因的RT-PCR和Western blot检测结果表明,经ATRA 处理后,感染Ad-NLS-RARα重组腺病毒的细胞C-MYC基因的mRNA和蛋白水平均高于其他两组(P<0.05)。结论 重组腺病毒Ad-NLS-RARα可以促进HL-60细胞的增殖,并通过上调C-MYC基因的表达,抑制ATRA诱导的HL-60细胞分化。  
    Abstract: Objective To explore the effect and mechanism of recombined adenovirus carrying NLS-RARα gene on proliferation of HL-60 cells and the differentiation of HL-60 cells induced by ATRA. Methods HL-60 cells was infected with Ad-NLS-RARα and control virus Ad-KZ. The efficiency of infection was detected by FCM. The mRNA and protein levels of NLS-RARα were assessed by Real-time PCR (RT-PCR) and Western blot, respectively. MTT assay were applied to determine proliferation of HL-60 cells. Cell surface differentiation antigen CD11b of infected HL-60 cell induced by ATRA was examined by FCM. The mRNA and protein levels of C-MYC of infected HL-60 cell induced by ATRA were determined by Real-time PCR (RT-PCR) and Western blot assay. Results The efficiency of infection of Ad-NLS-RARα and Ad-KZ on HL-60 cell was 70%-80%. The mRNA and protein levels of NLS-RARα gene of HL-60 cells which infected with Ad-NLS-RARα were both obviously higher than that of the cells which infected with Ad-KZ and non-infected (P<0.05). The proliferation ability of HL-60 cell infected with Ad-NLS-RARα was significantly increased (P<0.05). The level of CD11b of HL-60 cell infected with Ad-NLS-RARα and induced by ATRA was clearly decreased than control groups (P<0.05). The mRNA and protein levels of C-MYC gene of HL-60 cells infected with Ad-NLS-RARα and induced by ATRA were both obviously higher than that of the cells which infected with Ad-KZ and non-infected (P<0.05). Conclusion The recombined adenovirus Ad-NLS-RARα can increase the proliferation ability of HL-60 cell, and inhibit the differentiation of HL-60 cell through reduce the expression level of C-MYC gene.  
© 2013 《koko体育app 学报(医学版)》编辑部 版权所有 cc

开放获取🤪 本文遵循知识共享署名—非商业性使用4.0国际许可协议(CC BY-NC 4.0),允许第三方对本刊发表的论文自由共享(即在任何媒介以任何形式复制、发行原文)、演绎(即修改、转换或以原文为基础进行创作),必须给出适当的署名,提供指向本文许可协议的链接,同时标明是否对原文作了修改;不得将本文用于商业目的。CC BY-NC 4.0许可协议详情请访问

/

返回文章
返回
var _hmt = _hmt || []; (function() { var hm = document.createElement("script"); hm.src = "https://hm.baidu.com/hm.js?90c4d9819bca8c9bf01e7898dd269864"; var s = document.getElementsByTagName("script")[0]; s.parentNode.insertBefore(hm, s); })(); !function(p){"use strict";!function(t){var s=window,e=document,i=p,c="".concat("https:"===e.location.protocol?"https://":"http://","sdk.51.la/js-sdk-pro.min.js"),n=e.createElement("script"),r=e.getElementsByTagName("script")[0];n.type="text/javascript",n.setAttribute("charset","UTF-8"),n.async=!0,n.src=c,n.id="LA_COLLECT",i.d=n;var o=function(){s.LA.ids.push(i)};s.LA?s.LA.ids&&o():(s.LA=p,s.LA.ids=[],o()),r.parentNode.insertBefore(n,r)}()}({id:"K9y7iMpaU8NS42Fm",ck:"K9y7iMpaU8NS42Fm"}); koko体育-koko体育app koko体育-koko体育网页版koko体育app koko体育-全站app下载(官网) m6米乐app|下载 m6米乐app|主頁欢迎您!!