解剖学报 ›› 2016, Vol. 47 ›› Issue (4): 476-481.doi: 10.16098/j.issn.0529-1356.2016.04.007

• 细胞和分子生物学 • 上一篇    下一篇

β-神经生长因子基因克隆和诱导表达及其对PC12细胞的诱导分化作用

高杰1 严会文1 李红1 黄悦1 胡蓉1 苏敏1,2*   

  1. 1.贵州医科大学组织学胚胎学教研室,贵阳 550004; 2. 贵州医科大学贵州省细胞工程生物医药技术国家地方联合工程实验室, 贵州省再生医学重点实验室,贵阳 550004
  • 收稿日期:2015-12-07 修回日期:2016-02-05 出版日期:2016-08-06 发布日期:2016-08-06
  • 通讯作者: 苏敏 E-mail:summ30@163.com
  • 基金资助:

    贵州省优秀科技教育人才省长专项资金项目;贵州省科技厅-贵阳医学院联合基金

Inducing expression of β-neural growth factor and effect on PC12 cells

GAO Jie1 YAN Hui-wen1 LI Hong1 HUANG Yue1 HU Rong1 SU Min 1,2*   

  1. 1. Department of Histology and Embryology, Guizhou Medical University,Guiyang 550004,China; 2. National and Guizhou Joint Engineering Laboratory for Cell Engineering and Biomedicine Technique, Guizhou Province Key Laboratory of Regenerative Medicine, Guizhou Medical University, Guiyang 550004,China

  • Received:2015-12-07 Revised:2016-02-05 Online:2016-08-06 Published:2016-08-06
  • Contact: SU Min E-mail:summ30@163.com

摘要:

目的 构建β-神经生长因子(β-NGF)慢病毒表达载体pLVX-TRE3G-IRES-β-NGF,应用Tet-on 3G四环素诱导表达系统,探讨β-NGF在人胚肾(HEK293FT)细胞中的过表达情况,及其对大鼠肾上腺嗜铬细胞瘤(PC12)细胞分化的影响。方法 从SD大鼠脑组织提取总RNA,反转录成cDNA,利用分子生物学技术,克隆鼠β-NGF基因完整编码区,将β-NGF基因定向插入载体pLVX-TRE3G-IRES中。将重组载体pLVX-TRE3G-IRES-β-NGF和载体pLVXTet3G分别转染空白HEK293FT细胞,制备收获慢病毒,共转染HEK293FT细胞,同时用不同剂量强力霉素(Dox)诱导NGF表达(分为未转染组、0、100、500和1000μg/L Dox诱导表达组)。48h后收集细胞,免疫印迹法(Western blotting)检测各组细胞内βNGF表达情况。同时收集培养上清,1. ELISA检测各组上清内β-NGF的分泌量; 2. 制作条件培养基,加入PC12细胞培养基中进行诱导培养,观察PC12细胞诱导分化情况。 结果 双酶切和测序鉴定重组质粒pLVX-TRE3G-IRES-β-NGF序列和方向正确;β-NGF在转染细胞内被诱导表达,随着Dox剂量增加,表达量增强;β-NGF在培养基的上清内表达,表达量随Dox剂量增加而增多。诱导表达的条件培养基可诱导PC12细胞形态改变,表达神经元特异性烯醇化酶(NSE)蛋白。 结论 成功重组慢病毒载体 pLVX-TRE3G-IRES-β-NGF, 转染后β-NGF基因能够在HEK293FT细胞中表达和分泌,且该蛋白具有诱导PC12细胞向神经元样细胞分化的能力;运用Tet-On 3G四环素诱导表达系统,可成功诱导表达获得不同剂量β-NGF蛋白。

关键词: β-神经生长因子, PC12细胞, 强力霉素, 酶联免疫吸附法, 免疫印迹法, 大鼠

Abstract:

Objective To construct recombinant lentiviral vector carrying rat β-neural growth factor (β-NGF) gene by inducing expression of the Tet-on 3G tetracycline,and to observe its expression in HEK293FT cells and effects on PC12 cells. Methods Total RNA was extracted from rat brain as the template. By gene recombination technique,rat β-NGF gene was inserted into lentiviral vector as pLVX-TRE3G-IRES-β-NGF. The supernatant of virus including the recombinant vector of pLVX-TRE3G-IRES-β-NGF and pLVX-Tet3G was collected from packaging cells, respectively, and then cotransfected blank HEK293FT cells. The expression of β-NGF was induced with different doses of doxycycline (Dox) (divided into non-transfection group, 0, 100, 500 and 1000μg/L of Dox inducing group). Cells were collected and analyzed by Western blotting assay, 48 hours after. The supernatant was detected by ELISA assay for the secretion and used as conditional medium for PC12 cells. Results A band of β-NGF gene was about 726bp. After transfection, β-NGF protein was detected to express on 293FT cells and supernatant following the increase of Dox dose. The neuron-specific enolase (NSE) was expressed on PC12 cells after induced by conditional media. Conclusion That theβ-NGF gene was be expressed successfully on HEK 293FT cells by Tet-on 3G induced expression system, and the protein has effected on inducing PC12 cells differentiation into neuron-like cells.

Key words: β-Nerve growth factor, PC12 cell, Doxycycline, ELISA, Western blotting, Rat