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hVDR原核表达及其与重金属镉、 铅的结合活性
引用本文:焦健,张照斌,胡建英,王金水. hVDR原核表达及其与重金属镉、 铅的结合活性[J]. 环境科学, 2010, 31(10): 2469-2474
作者姓名:焦健  张照斌  胡建英  王金水
作者单位:1. 河南工业大学粮油食品学院,郑州,450052;北京大学城市与环境学院,北京,100871
2. 北京大学城市与环境学院,北京,100871
3. 河南工业大学粮油食品学院,郑州,450052
基金项目:国家自然科学基金项目(20877003,20837003)
摘    要:

关 键 词:人维生素D受体;原核表达;重金属;结合效应;镉;铅   骨代谢
收稿时间:2009-11-24
修稿时间:2010-01-16

Prokaryotic Expression of Human Vitamin D Receptor (hVDR) and Its Binding Activities to Cd and Pb
JIAO Jian,ZHANG Zhao-bin,HU Jian-ying and WANG Jin-shui. Prokaryotic Expression of Human Vitamin D Receptor (hVDR) and Its Binding Activities to Cd and Pb[J]. Chinese Journal of Environmental Science, 2010, 31(10): 2469-2474
Authors:JIAO Jian  ZHANG Zhao-bin  HU Jian-ying  WANG Jin-shui
Affiliation:School of Food Science and Technology, Henan University of Technology, Zhengzhou 450052, China. jiaojian1111@yahoo.com.cn
Abstract:Human vitamin D receptor (hVDR) is a potential receptor channel for heavy metals to affect bone metabolism, while to date there is no report about the binding activity between heavy metals and hVDR. This study established a prokaryotic expression of hVDR system, by cloned hVDR-LBD into pGEX-4T-1 vector. Then according to the principle that the nuclear receptor binding with its ligand can be combined with nuclear receptor coactivator 2-bacterial alkaline phosphatase fusion protein (TIF2-BAP), we established a method of p-nitrophenylphosphate-alkaline phosphatase to analyse the effects of chemical on the binding activity between hVDR and TIF2-BAP. Using this method, we studied the binding activities between hVDR and TIF2-BAP after exposure of cadmium and lead. The results showed that the binding activities significantly increased to 3.95 and 4.39 times that of the control after exposure of 100 micromol/L and 1 000 micromol/L cadmium chloride (CdCl2), and the binding activities significantly increased to 2.29 and 3.52 times that of the control after exposure of 100 micromol/L and 1 000 micromol/L lead acetate (PbAc2), respectively. These results indicate that cadmium and lead can mimic the activity of 1,25-(OH)2D3, disrupt the normal function of hVDR receptor channel, which may be the underlying mechanism of abnormal bone metabolism and osteoporosis caused by cadmium and lead.
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