位置:成果数据库 > 期刊 > 期刊详情页
腺病毒介导的野生型PTEN抑制活化肝星状细胞系HSC—T6增殖的机制
  • ISSN号:1007-3418
  • 期刊名称:《中华肝脏病杂志》
  • 时间:0
  • 分类:R730.264[医药卫生—肿瘤;医药卫生—临床医学]
  • 作者机构:[1]河北联合大学附属医院消化内科,河北省唐山市063000, [2]河北医科大学第二医院消化内科, [3]河北省消化病重点实验室河北省消化病研究所
  • 相关基金:国家自然科学基金(30872513)
中文摘要:

目的通过检测腺病毒介导的野生型第10号染色体缺失的磷酸酶张力蛋白同源物基因(PTEN)对体外活化肝星状细胞(HSC)细胞周期的影响,探讨过表达的野生型PTEN抑制活化HSC增殖的可能机制。方法体外培养肝星状细胞系HSC-T6,以腺病毒为载体将野生型PTEN基因瞬时转染活化HSC,实验分为空白对照组、Ad-GFP组和Ad-PTEN组。流式细胞术测定HSC细胞周期时相,Western blot及实时定量PCR检测HSC的PTEN表达量,Western blot检测HSC的细胞周期素D1(cyclin D1)和细胞周期素依赖性激酶4(CDK4)表达水平。多组间比较采用单因素方差分析,组间比较采用Tukey检验。结果携带野生型PTEN基因的腺病毒(AD-PTEN)成功转染HSC,Ad-FTEN组G0/G1期HSC细胞数(67.68%+2.75%)较对照组(53.01%±2.37%)及Ad-GFP组(53.85%±3.08%)明显增高(F=38.59,P〈0.01);S期HSC细胞数(14.42%±1.81%)较对照组(22.17%±1.99%)及Ad-GFP组(21.54%±1.74%)明显降低(F=18.85,P〈0.01);G2/M期HSC细胞数(17.90%±2.70%)较对照组(24.82%±3.81%)及Ad-GFP组(24.62%±3.15%)明显降低(F=7.17,P〈0.01)。腺病毒感染HSC后72h,Ad-PTEN组cyclin D1的相对表达量(1.12±0.07)较对照组(1.45±0.05)及Ad-GFP组(1.47±0.08)明显降低(F=42.86,P〈0.01),CDK4相对表达量(1.05±0.07)较对照组(1.41±0.03)及Ad-GFP组(1.43±0.06)也明显降低(F=67.01,P〈0.01)。结论过表达的野生型PTEN通过下调cyclin D1和CDK4的表达,明显抑制体外活化HSC细胞周期的G1/S期转化,阻滞HSC细胞周期时相于G0/G1期,进而抑制其增殖。

英文摘要:

Objective Using an adenoviral vector, the wild-type PTEN gene was transduced into activated hepatic stellate cell (HSC) culcured in vitro and cell cycle markers and were detect. Thereby, the potential mechanisms of inhibitory effect of the wild-type PTEN overexpression on the proliferation in activated HSC was investigated. Methods The wild type PTEN gene was transduced into activated HSC (HSC-T6) cultured in vitro mediated by adenoviral vector. PTEN expression in HSC was measured by Western blot and Real-time fluorescent quantitation PCR. Flow cytometry (FCM) was then used to detect cell cycle phase of activated HSC. And the expressions of cyclinD1 and cyclin dependent kinase 4 (CDK4)in HSC were determined by Western blot. Results The data showed that exogenous wild type PTEN gene was successfully transduced and expressed in activated HSC cultured in vitro. The over-expression of wild type PTEN resulted in the increased number of HSC at G0/G1 phase (P〈0.01), and the number of HSC at S phase and G2/M phase were decreased significantly, P〈0.01. Furthermore, there were decreased cyclinD1 and CDK4 expression in HSC infected with Ad-PTEN, P〈 0.01. Conclusion The over-expression of wild type PTEN inhibit transition of activated HSC in vitro from G1 to S phase and arrest cell cycle of them at G0/G1 phase via the down-regulated expressions of cyclinD 1 and CDK4, and then inhibit HSC proliferation.

同期刊论文项目
同项目期刊论文
期刊信息
  • 《中华肝脏病杂志》
  • 北大核心期刊(2011版)
  • 主管单位:中国科学技术协会
  • 主办单位:中华医学会
  • 主编:
  • 地址:重庆市渝中区临江路74号
  • 邮编:400010
  • 邮箱:chnhepa@online.cq.cn
  • 电话:023-63706512
  • 国际标准刊号:ISSN:1007-3418
  • 国内统一刊号:ISSN:50-1113/R
  • 邮发代号:78-56
  • 获奖情况:
  • 中国期刊方阵“双效”期刊
  • 国内外数据库收录:
  • 美国化学文摘(网络版),荷兰文摘与引文数据库,美国生物医学检索系统,日本日本科学技术振兴机构数据库,中国中国科技核心期刊,中国北大核心期刊(2004版),中国北大核心期刊(2008版),中国北大核心期刊(2011版),中国北大核心期刊(2014版)
  • 被引量:47128