Liu Jie, Peng Na, Zeng Shunfu, Lu Yan, Wang Jian, Zhou Yue
Department of Orthopaedics, Xinqiao Hospital, the Third Military Medical University, Chongqing, 400037, PR China.
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2012 Feb;26(2):166-71.
To detect the expression of Bcl-2/adenovirus E1B 19-kDa-interacting protein 3 (BNIP3) in cell death induced by nutrition deprivation in nucleus pulposus cells so as to further understand the mechanism of death in nucleus pulposus cells.
Two adult Sprague Dawley rats, male or female, weighing 150-200 g, were involved in this experiment. The cells isolated from rat caudal disc were cultured under the condition of L-DMEM culture media, 10%FBS, and 21%O2 (control group) and under the condition of DMEM-free glucose culture media, no serum, and 1% 02 (experimental group). The expressions of BNIP3 gene and protein were detected by real-time fluorescent quantitative PCR, immunofluorescence staining, and Western blot. The cell apoptosis rate and mitochondrial membrane potential were measured by flow cytometry at 24, 48, and 72 hours after culture.
The expression of BNIP3 decreased in the control group; the expressions of BNIP3 showed an increasing tendency with time in the experimental group, and BNIP3 combined with mitochondria. Significant differences were observed in the expressions of BNIP3 gene and protein between 2 groups at the other time (P < 0.05) except that no significant difference was observed in the expression of BNIP3 gene at 24 hours (P > 0.05). The cell apoptosis rate and mitochondrial membrane potential were significantly lower in the experimental group than those in the control group (P < 0.05).
Upregulation of BNIP3 and translocation to mitochondria may be involved in nucleus pulposus cell death in nutrition deprivation.
检测Bcl-2/腺病毒E1B 19-kDa相互作用蛋白3(BNIP3)在髓核细胞营养剥夺诱导的细胞死亡中的表达,以进一步了解髓核细胞的死亡机制。
本实验选用2只体重150-200 g的成年Sprague Dawley大鼠,雌雄不限。将从大鼠尾椎间盘分离的细胞在L-DMEM培养基、10%胎牛血清和21%氧气条件下培养(对照组),以及在无葡萄糖的DMEM培养基、无血清和1%氧气条件下培养(实验组)。通过实时荧光定量PCR、免疫荧光染色和蛋白质印迹法检测BNIP3基因和蛋白的表达。在培养24、48和72小时后,通过流式细胞术测量细胞凋亡率和线粒体膜电位。
对照组中BNIP3的表达降低;实验组中BNIP3的表达随时间呈增加趋势,且BNIP3与线粒体结合。除24小时时BNIP3基因表达无显著差异(P>0.05)外,两组在其他时间的BNIP3基因和蛋白表达均有显著差异(P<0.05)。实验组的细胞凋亡率和线粒体膜电位显著低于对照组(P<0.05)。
BNIP3的上调和向线粒体的转位可能参与了营养剥夺时髓核细胞的死亡。