Yang K C, Liu L M, Li P, Dong L X, Zhou G Y, Tian Z Y, Luo C, Xia T, Wang A G, Zhang S
MOE Key Lab of Environment and Health, Department of Occupational and Environmental Health, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2019 Jan 20;37(1):1-6. doi: 10.3760/cma.j.issn.1001-9391.2019.01.001.
To investigate the effect of 2, 2', 4, 4'-tetrabromodiphenyl ether (PBDE-47) on the mitochondrial mass in rat adrenal pheochromocytoma (PC12) cells and the potential mechanisms. Highly differentiated PC12 cells were divided into control, 1, 10 or 20 μmol/L PBDE-47-treated groups and cultured for 24 h. Transmission electron microscopy was employed to observe the changes in mitochondrial morphology and quantity in PC12 cells. Flow cytometry was used to measure the fluorescence intensity of Nonyl Acridine Orange (NAO) , a fluorescent indicator of mitochondrial membrane cardiolipin, to reflect mitochondria mass. Western blotting was used to determine the expression levels of Mitofusion 1 (Mfn1) and Fission 1 (Fis1) proteins. To further explore the role of abnormal mitochondrial fusion and fission in PBDE-47-induced mitochondrial mass changes, PC12 cells were divided into control group, 5 μmol/L M1 treatment group, 20 μmol/L PBDE-47 treatment group and 5 μmol/L M1+20 μmol/L PBDE-47 combined treatment group and cultured for 24 h, then the fluorescence intensity of NAO and expression levels of Mfn1 and Fis1 proteins were detected. The control group showed numerous mitochondria with normal morphology, while the number of mitochondria decreased after PBDE-47 treatment. Especially, the disappeared cristae, swelling and vacuoles of mitochondria and decreased fluorescence intensity of NAO (<0.05) were observed in 10 and 20 μmol/L PBDE-47-treated groups. Meanwhile, the expression levels of Mfn1 and Fis1 proteins in the 10 and 20 μmol/L PBDE-47-treated groups were significantly decreased compared with control group (<0.05) . However, 5 μmol/L M1 co-treatment with 20 μmol/L PBDE-47 significantly increased the levels of Mfn1 and Fis1 proteins and fluorescence intensity of NAO compared with the 20 μmol/L PBDE-47 group (<0.05) . PBDE-47 can inhibit the mitochondrial fusion and fission process, thus leading to damage of mitochondria mass in PC12 cells.
研究2,2',4,4'-四溴二苯醚(PBDE-47)对大鼠肾上腺嗜铬细胞瘤(PC12)细胞线粒体质量的影响及其潜在机制。将高度分化的PC12细胞分为对照组、1、10或20 μmol/L PBDE-47处理组,培养24小时。采用透射电子显微镜观察PC12细胞线粒体形态和数量的变化。使用流式细胞术测量线粒体膜心磷脂荧光指示剂壬基吖啶橙(NAO)的荧光强度,以反映线粒体质量。采用蛋白质免疫印迹法检测线粒体融合蛋白1(Mfn1)和分裂蛋白1(Fis1)的表达水平。为进一步探讨线粒体融合和分裂异常在PBDE-47诱导的线粒体质量变化中的作用,将PC12细胞分为对照组、5 μmol/L M1处理组、20 μmol/L PBDE-47处理组和5 μmol/L M1+20 μmol/L PBDE-47联合处理组,培养24小时,然后检测NAO荧光强度以及Mfn1和Fis1蛋白的表达水平。对照组线粒体数量众多,形态正常,而PBDE-47处理后线粒体数量减少。特别是,在10和20 μmol/L PBDE-47处理组中观察到线粒体嵴消失、肿胀和空泡形成,且NAO荧光强度降低(<0.05)。同时,与对照组相比,10和20 μmol/L PBDE-47处理组中Mfn1和Fis1蛋白的表达水平显著降低(<0.05)。然而,与20 μmol/L PBDE-47组相比,5 μmol/L M1与20 μmol/L PBDE-47联合处理显著增加了Mfn1和Fis1蛋白水平以及NAO荧光强度(<0.05)。PBDE-47可抑制线粒体融合和分裂过程,从而导致PC12细胞线粒体质量受损。