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1.400038 重庆,陆军军医大学(第三军医大学)第一附属医院骨科
2.401120 重庆,重庆医科大学附属第三医院骨与创伤中心
[周强,E-mail: zq_tlh@163.comZHOU Qiang, E-mail: zq_tlh@163.com
收稿:2019-12-13,
修回:2020-02-02,
纸质出版:2020-05-15
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张泽桐, 房朗, 甘翼博, 等. 水通道蛋白3在高渗环境诱导髓核细胞凋亡中的作用[J]. 第三军医大学学报, 2020,42(9):915-922.
Zetong ZHANG, Lang FANG, Yibo GAN, et al. Role of aquaporin-3 in hyperosmolarity-induced apoptosis of rat nucleus pulposus cells
张泽桐, 房朗, 甘翼博, 等. 水通道蛋白3在高渗环境诱导髓核细胞凋亡中的作用[J]. 第三军医大学学报, 2020,42(9):915-922. DOI: 10.16016/j.1000-5404.201912129.
Zetong ZHANG, Lang FANG, Yibo GAN, et al. Role of aquaporin-3 in hyperosmolarity-induced apoptosis of rat nucleus pulposus cells
目的
2
研究水通道蛋白3(aquaporin-3,AQP-3)在高渗透压诱导的大鼠髓核细胞(rat nucleus pulposus)凋亡中的作用。
方法
2
体外培养的大鼠髓核细胞,按330、550 mOsm/kg的渗透压分组,CCK-8检测髓核细胞增殖,流式细胞分析细胞凋亡率,Western blot和定量PCR检测凋亡相关分子Bcl-2、Bax和caspase3表达情况;使用免疫细胞化学、Western blot和定量PCR检测AQP-3的表达。利用过表达慢病毒提高AQP-3的表达,进一步观察AQP-3对高渗环境诱导凋亡的影响。
结果
2
相比于330 mOsm/kg渗透压,550 mOsm/kg高渗环境中髓核细胞培养12、24、48、72 h细胞增殖显著降低,髓核细胞凋亡率显著增加(
P
<
0.05),蛋白和mRNA表达结果显示Bcl-2表达明显降低(
P
<
0.05),Bax和cleaved caspase 3/caspase 3表达明显增加(
P
<
0.05)。相比于高渗环境中的空白对照髓核细胞,AQP-3过表达髓核细胞的凋亡率显著降低(
P
<
0.05),蛋白和mRNA表达结果显示Bcl-2表达明显增加(
P
<
0.05),Bax和cleaved caspase 3/caspase 3表达明显降低(
P
<
0.05)。
结论
2
高渗透压显著促进髓核细胞的凋亡并降低AQP-3的表达;过表达AQP-3可缓解高渗透压环境下髓核细胞凋亡。
Objective
2
To investigate the role of aquaporin-3 (AQP-3) in hyperosmolarity-induced apoptosis of cultured rat nucleus pulposus (NP) cells.
Methods
2
Rat NP cells were cultured under different osmotic pressures (330 and 550 mOsm/kg)
and the proliferation and apoptotic rate of the cells were determined using CCK-8 assay and flow cytometry
respectively. Western blotting and real-time quantitative PCR were used to detect the expression levels of apoptosis-related molecules (Bcl-2
Bax
cleaved caspase 3/caspase 3)
and immunocytochemistry
Western blotting and real-time quantitative PCR were used to detect the expression of AQP-3 in the cells. The effect of lentivirus-mediated AQP-3 overexpression on apoptosis of NP cells was investigated after hyperosmolar exposure.
Results
2
An osmotic pressure of 550 mOsm/kg
as compared with 330 mOsm/kg
significantly decreased NP cell proliferation
increased the
cell apoptotic rate
upregulated the expression of the pro-apoptotic molecules Bax and cleaved caspase 3/caspase 3 (
P
<
0.05)
and down-regulated the expression of the anti-apoptotic molecule Bcl-2 (
P
<
0.05). The cells with lentivirus-mediated AQP-3 overexpression showed an obviously lowered apoptotic rate following the hyperosmolar exposure and significantly reduced expression of Bax and cleaved caspase 3/caspase 3 (
P
<
0.05) with an enhanced expression of Bcl-2 (
P
<
0.05).
Conclusion
2
Hyperosmolar exposure significantly promotes apoptosis of NP cells and reduce the expression of AQP-3. AQP-3 overexpression can partly attenuate apoptosis of NP cells following a hyperosmolar exposure.
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