Wang Yun, Li Qingshu, Jia Chao, Xie Chunyu, Song Yankun, Zhang Nan, Qu Yan
School of Nursing, Medical College of Qingdao University, Qingdao 266023, Shandong, China (Wang Y, Xie CY, Song YK, Zhang N); Department of Critical Care Medicine, Affiliated Qingdao Municipal Hospital of Qingdao University, Qingdao 266071, Shandong, China (Li QS, Jia C, Qu Y). Corresponding author: Qu Yan, Email:
Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2017 Mar;29(3):239-243. doi: 10.3760/cma.j.issn.2095-4352.2017.03.009.
To investigate the protective effects of lentivirus mediated Bcl-2-associated athanogene 1L (BAG-1L) over-expression on human neuroblastoma cells (SH-SY5Y) induced by hypoxia/re-oxygenation, and to study its effect on the phosphoinositide 3 kinase serine/threonine protein kinase (PI3K/AKT) pathway.
SH-SY5Y cells were cultured in vitro, and the cells at logarithmic phase were collected, and they were divided into recombined lentiviral infection group [infected by lentivirus containing BAG-1L and green fluorescent protein (GFP) gene], vector control group (infected by lentivirus containing GFP without BAG-1L gene) and cell control group (non-infection). Western Blot was used to detect the expression of BAG-1L in target cells after infection for 48 hours. SH-SY5Y cells were subjected to hypoxia for 8 hours and re-oxygenation for 24 hours, then the cell counting kit-8 (CCK-8) was used to detect the cell activity, and the apoptosis was detected by flow cytometry after allophycocyanin labeled annexin V/7-amino actinomycin D (Annexin V-APC/7-AAD) staining. Western Blot was used to detect the protein expressions of BAG-1L, heat shock protein 70 (HSP70), AKT and phosphorylated AKT (p-AKT).
After infection for 48 hours, exogenous BAG-1L protein bands were observed in recombined lentiviral infection group, but not observed in cell control group and vector control group. After hypoxia/re-oxygenation treatment, the cell viability in recombined lentiviral infection group was significantly higher than that in cell control group and vector control group (A value: 0.689±0.036 vs. 0.425±0.013, 0.400±0.012), apoptosis was significantly decreased [apoptosis rate: (26.97±1.82)% vs. (36.60±1.45)%, (35.77±3.74)%], the protein levels of BAG-1L, HSP70 and p-AKT were significantly increased [BAG-1L protein (gray value): 2.405±0.167 vs. 0.529±0.141, 0.601±0.099; HSP70 protein (gray value): 0.997±0.123 vs. 0.634±0.091, 0.584±0.106; p-AKT protein (gray value): 1.234±0.118 vs. 0.661±0.210, 0.712±0.199, all P < 0.01], but the protein level of AKT was slightly increased (gray value: 1.103±0.269 vs. 0.646±0.188, 0.791±0.326) without statistically significant differences (both P > 0.05). There was no significant difference in all parameters between cell control group and vector control group (all P > 0.05).
Lentivirus mediated BAG-1L gene over-expression can protect nerve cells against hypoxic injury and apoptosis, and the protective effect may be related to the activation increase of pathway on PI3K/AKT.
探讨慢病毒介导的Bcl-2相关抗凋亡基因1L(BAG-1L)过表达对缺氧/复氧诱导的人神经母细胞瘤细胞(SH-SY5Y)的保护作用,并研究其对磷酸肌醇3激酶丝氨酸/苏氨酸蛋白激酶(PI3K/AKT)通路的影响。
体外培养SH-SY5Y细胞,收集对数期细胞,分为重组慢病毒感染组(感染含BAG-1L和绿色荧光蛋白基因的慢病毒)、载体对照组(感染含绿色荧光蛋白而无BAG-1L基因的慢病毒)和细胞对照组(未感染)。采用蛋白质免疫印迹法检测感染48小时后靶细胞中BAG-1L的表达。将SH-SY5Y细胞进行8小时缺氧和24小时复氧处理,然后用细胞计数试剂盒-8(CCK-8)检测细胞活性,用别藻蓝蛋白标记的膜联蛋白V/7-氨基放线菌素D(Annexin V-APC/7-AAD)染色后通过流式细胞术检测细胞凋亡。采用蛋白质免疫印迹法检测BAG-1L、热休克蛋白70(HSP70)、AKT及磷酸化AKT(p-AKT)的蛋白表达。
感染48小时后,重组慢病毒感染组观察到外源性BAG-1L蛋白条带,而细胞对照组和载体对照组未观察到。缺氧/复氧处理后,重组慢病毒感染组细胞活力显著高于细胞对照组和载体对照组(A值:0.689±0.036比0.425±0.013、0.400±0.012),凋亡显著减少[凋亡率:(26.97±1.82)%比(36.60±1.45)%、(35.77±3.74)%],BAG-1L、HSP70及p-AKT蛋白水平显著升高[BAG-1L蛋白(灰度值):2.405±0.167比0.529±0.141、0.601±0.099;HSP70蛋白(灰度值):0.997±0.123比0.634±0.091、0.584±0.106;p-AKT蛋白(灰度值):1.234±0.118比0.661±0.210、0.712±0.199,均P<0.01],但AKT蛋白水平略有升高(灰度值:1.103±0.269比0.646±0.188、0.791±0.326),差异无统计学意义(均P>0.05)。细胞对照组和载体对照组各项参数比较差异均无统计学意义(均P>0.05)。
慢病毒介导的BAG-1L基因过表达可保护神经细胞免受缺氧损伤及凋亡,其保护作用可能与PI3K/AKT通路的激活增强有关。