Li Ping, Zhong Xue-yun, He Li-zhen, Lin Chen-li
Department of Pathology, Jinan University Medical College, Guangzhou, China.
Zhonghua Zhong Liu Za Zhi. 2007 Apr;29(4):245-8.
To investigate the biological effects of PTEN gene on the malignant glioma cell line SHG-44. Firstly, A recombinant eukaryotic expression plasmid containing PTEN gene fused with EGFP (enhanced green fluorescence protein) gene was constructed. Secondly, the expression of the recombinant vector in human glioma cells was detected.
(1) The human PTEN gene was amplified by RT-PCR and inserted into pEGFP-N1 that was selected by T-A subclone, and the recombinant expression vector was obtained. After the recombinant plasmids were transfected into glioma SHG-44 cells by cation polymex, expression of fusion protein was tested. (2) The stable transfected cells were selected by G418 and amplified. Light microscopy and growth curve were used to measure the effects of PTEN expression on cell morphology and proliferation. Expression of GFAP (glial fibillary acidic protein) was detected immunohistochemically.
(1) The positive recombinant was sequenced and demonstrated to have the same sequence as that of PTEN gene in GenBank. It was proved that the eukaryotic expression vector pEGFP-PTEN have been constructed successfully and expressed in SHG-44 cells. (2) The SHG-44 cell growth was changed obviously. The expression of GFAP was increased.
The construction of PTEN eukaryotic expression vector containing green fluorescence protein gene will lay the basis for carrying out further studies on the function of PTEN gene.
研究PTEN基因对恶性胶质瘤细胞系SHG-44的生物学作用。首先,构建一种含有与增强型绿色荧光蛋白(EGFP)基因融合的PTEN基因的重组真核表达质粒。其次,检测重组载体在人胶质瘤细胞中的表达。
(1)通过RT-PCR扩增人PTEN基因,并将其插入经T-A亚克隆筛选的pEGFP-N1中,获得重组表达载体。将重组质粒通过阳离子聚合物转染到胶质瘤SHG-44细胞中后,检测融合蛋白的表达。(2)用G418筛选稳定转染的细胞并进行扩增。用光镜和生长曲线来测定PTEN表达对细胞形态和增殖的影响。免疫组织化学法检测胶质纤维酸性蛋白(GFAP)的表达。
(1)对阳性重组体进行测序,结果显示其序列与GenBank中PTEN基因的序列相同。证明真核表达载体pEGFP-PTEN构建成功并在SHG-44细胞中表达。(2)SHG-44细胞的生长明显改变。GFAP的表达增加。
含绿色荧光蛋白基因的PTEN真核表达载体的构建将为进一步研究PTEN基因的功能奠定基础。