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作 者:吕文杰[1,2] 王洪涛[2] 黄芳[2] 王健[2] 王芃[2] 洪鎏[1] 周建光[2] 潘耀振[1] 李山虎[2]
机构地区:[1]贵州医科大学,贵州贵阳550001 [2]军事医学科学院生物工程研究所,北京100850
出 处:《生物技术通讯》2016年第1期27-31,共5页Letters in Biotechnology
基 金:国家自然科学基金(81470138;81372770;81372140)
摘 要:目的:构建过表达血清与糖皮质激素调节激酶3(SGK3)的质粒以及稳定表达SGK3的肝癌细胞系BEL-7402,研究其在去甾体激素胎牛血清(FBS)中的抗凋亡能力。方法:PCR扩增SGK3基因,将扩增产物连接到p CDH载体,构建出p CDH-SGK3的慢病毒载体质粒,将其同空白对照p CDH-NC分别与慢病毒包装载体共转入293T细胞,包装成慢病毒p CHD-SGK3和p CDH-NC;将构建的慢病毒感染肝癌细胞BEL-7402并用嘌呤霉素筛选,Western印迹检测SGK3的表达;观察细胞在FBS及去甾体激素FBS中的生长情况。结果:包装出p CDH-SGK3重组慢病毒,此慢病毒感染肝癌细胞系BEL-7402后获得表达;CCK8实验表明过表达SGK3可促进肝癌细胞的生长,BEL-7042细胞中有雄激素的表达,去甾体激素FBS中细胞生长受到抑制,过表达SGK3可增强肝癌细胞在去甾体激素血清中的抗凋亡能力。结论:在肝癌细胞BEL-7402中过表达SGK3可促进细胞生长,可增强细胞在去甾体激素FBS中的抗凋亡能力。Objective: To construct the vector carrying serum and glucorticoid regulated kinase 3(SGK3) coding sequence and to build BEL-7402 cell line stably overexpressing SGK3 protein, to study the anti-apoptosis ability of this cell line growing in charcoal stripped fetal bovine serum(FBS). Methods: SGK3 gene was amplified by PCR and then linked to vector pCDH to construct the lentivirus vector of pCDH-SGK3. Vector pCDH-SGK3 and its empty vector pCDH-NC were respectively co-transfeeted into cells 293T with packaging carriers to produce len- tivirus-SGK3 and lentivirus-NC. Cells BEL-7402 were infected with produced lentivirus and filtered with puromy- cin. The expression level of SGK3 was tested by Western blot. Cell was cultured in DMEM with 10% FBS and 10% charcoal striped FBS respectively. Results: The vector carrying SGK3 coding sequence was successfully con- structed and BEL-7402 cell line stably overexpressing SGK3 protein was constructed. SGK3 could enhance the growth of cell BEL-7402, androgen receptor and the ability of anti-apoptosis cultured in the DMEM with 10% charcoal striped FBS. Conclusion: Overexpression of SGK3 in hepatocellular carcinoma cell could enhance its growth and the ability of anti-apoptosis cultured in the DMEM with 10% charcoal striped FBS.
关 键 词:血清与糖皮质激素调节激酶3 肝癌 BEL-7402细胞 去甾体激素胎牛血清
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