Qiu Xiu-chun, Yu Cui-juan, Meng Yan-ling, Xu Yan-ming, Zhao Jing, Jin Ming, Wang Cheng-ji, Fan Qing-yu, Yang An-gang
Department of Biochemistry and Molecular Biology, Fourth Military Medical University, Xi'an 710032, China.
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2004 Jan;20(1):19-22.
To explore the expression of the truncated bid gene and its pro-apoptotic effect on Hela cells.
A full-length human bid gene was cloned by RT-PCR and confirmed by sequence analysis. By deleting the 60 amino acids of N-terminal the truncated bid (tbid) gene was obtained and then inserted into the eukaryotic expression vector pIRES2-EGFP. After the tbid gene was transfected into Hela cells under lipofectamine mediation, the effect of target gene expression on morphology and growth of Hela cells were observed under fluorescence and electron microscopes and analysed by TUNEL staining.
pIRES2-EGFP containing tbid gene was constructed successfully. After Hela cells were transfected with GFP expression vector of tbid gene, tbid was expressed which was followed by decreased cell fluorescence intensity, poor cell growth, and cell death. Cell shrinkage and nuclear condensation, typical apoptotic characteristics, were observed by electron microscope observation and Tunel staining.
The expression of tbid can effectively induce apoptosis of Hela cells.
探讨截短型bid基因的表达及其对Hela细胞的促凋亡作用。
通过RT-PCR克隆人bid基因全长,并经序列分析证实。删除N端60个氨基酸获得截短型bid(tbid)基因,然后将其插入真核表达载体pIRES2-EGFP。在脂质体介导下将tbid基因转染至Hela细胞后,在荧光显微镜和电子显微镜下观察目的基因表达对Hela细胞形态和生长的影响,并通过TUNEL染色进行分析。
成功构建了含tbid基因的pIRES2-EGFP。用tbid基因的GFP表达载体转染Hela细胞后,tbid表达,随后细胞荧光强度降低、细胞生长不良及细胞死亡。通过电子显微镜观察和Tunel染色观察到细胞皱缩和核固缩等典型凋亡特征。
tbid的表达可有效诱导Hela细胞凋亡。