Qin Haihong, Shen Hui, Wang Fudi, Guo Junsheng
Department of Military Hygiene, Second Military Medical University, Shanghai 200433, China.
Wei Sheng Yan Jiu. 2004 Sep;33(5):562-4.
To study the homeostasis of zinc in central nervous system.
Expression of MT1/MT2/MT3 on various concentration of zinc exposure (0-150 micromol/L) was determined and their expression on 100 micromol/L zinc exposure after 0, 2, 4, 6 and 8 hours in primary culture rat hippocampal neurons was measured by real-time fluorescent quantitative RT-PCR.
Amount of MT3 mRNA was highest followed by MT1 mRNA, MT2 mRNA ranked third. Expression of MT1 and MT2 mRNA could be up-regulated significantly on 75-100 micromol/L zinc exposure, and then, reach to a plateau on 125-150 micromol/L. Their peak mRNA levels appeared at about 6 h after addition of zinc was added. However, the MT3 mRNA was decreased by about 60% after zinc was added 6 h later.
The results showed that not only the MT3 but also the MT1 and MT2 were involved in the regulation of zinc homeostasis in neurons, just like neuroglial cell do.
研究中枢神经系统中锌的稳态。
通过实时荧光定量逆转录聚合酶链反应测定原代培养大鼠海马神经元在不同浓度锌暴露(0 - 150微摩尔/升)下MT1/MT2/MT3的表达,并检测在100微摩尔/升锌暴露0、2、4、6和8小时后的表达情况。
MT3 mRNA量最高,其次是MT1 mRNA,MT2 mRNA排第三。在75 - 100微摩尔/升锌暴露时,MT1和MT2 mRNA的表达可显著上调,然后在125 - 150微摩尔/升时达到平台期。它们的mRNA峰值水平在添加锌后约6小时出现。然而,在添加锌6小时后,MT3 mRNA下降约60%。
结果表明,MT3以及MT1和MT2都参与神经元中锌稳态的调节,就像神经胶质细胞一样。