Shi Zeyu, Zhan Yaqi, Zhao Junxing, Wang Jinming, Ma Haili
College of Animal Science and Veterinary Medicine, Shanxi Agriculture University, Taigu, Jinzhong, Shanxi, (030800), China.
Biol Trace Elem Res. 2016 Oct;173(2):333-8. doi: 10.1007/s12011-016-0656-9. Epub 2016 Feb 23.
This study investigated the effects of sodium fluoride on the expression of p38MAPK signaling pathway-related genes and proteins in the spleen lymphocytes of mice, revealing the mechanism of the toxicity of fluoride to the immune system. The spleen lymphocytes, isolated from mice consuming different NaF doses (0, 50, 100, and 150 mg/L) for 60 days, were cultured in medium with bacteria lipopolysaccharide, and the cells' proliferation ability was analyzed through MTT; real-time PCR detected the change of MLK3/MKK6/p38MAPK/MSK1/ATF1 on mRNA, and the difference of protein expression of MKK6/p38MAPK were detected through the Western blotting. The results suggested that the proliferation ability of spleen lymphocytes isolated from mice consuming different NaF doses is lower, and the expression of genes and proteins of MKK6/p38MAPK showed a decreasing trend. These results demonstrate that fluoride can suppress the activation of p38MAPK pathway in mice spleen lymphocytes and further influences the function of the immune system.
本研究探讨了氟化钠对小鼠脾脏淋巴细胞中p38丝裂原活化蛋白激酶(p38MAPK)信号通路相关基因和蛋白表达的影响,揭示氟对免疫系统毒性作用的机制。从饮用不同剂量氟化钠(0、50、100和150mg/L)60天的小鼠中分离出脾脏淋巴细胞,在含有细菌脂多糖的培养基中培养,通过MTT法分析细胞增殖能力;实时定量聚合酶链反应(real-time PCR)检测MLK3/MKK6/p38MAPK/MSK1/ATF1 mRNA的变化,通过蛋白质免疫印迹法(Western blotting)检测MKK6/p38MAPK蛋白表达差异。结果表明,不同氟化钠剂量组小鼠脾脏淋巴细胞增殖能力降低,MKK6/p38MAPK基因和蛋白表达呈下降趋势。这些结果表明,氟可抑制小鼠脾脏淋巴细胞中p38MAPK通路的激活,进而影响免疫系统功能。