Reduction of neuropathy target esterase does not affect neuronal differentiation, but moderate expression induces neuronal differentiation in human neuroblastoma (SK-N-SH) cell line

被引:23
作者
Chang, PA
Chen, R
Wu, YJ [1 ]
机构
[1] Chinese Acad Sci, Mol Toxicol Lab, State Key Lab Integrated Management Pest Insects, Inst Zool, Beijing 100080, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
来源
MOLECULAR BRAIN RESEARCH | 2005年 / 141卷 / 01期
基金
中国国家自然科学基金;
关键词
neuropathy target esterase; neural differentiation; human neuroblastoma cell; RNA interference; organophosphate;
D O I
10.1016/j.molbrainres.2005.07.012
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Neuropathy target esterase (NTE) is inhibited and aged by organophosphorus compounds that induce delayed neuropathy in human and some sensitive animals. NTE has been proposed to play a role in neurite outgrowth and process elongation during neurodifferentiation. However, to date, there is no direct evidence of the relevance of NTE in neurodifferentiation under physiological conditions. In this study, we have investigated a possible role for NTE in the all-trans retinoic acid-induced differentiation of neuroblastoma cells. The functional inactivation of NTE by RNA interference indicated that reduction of NTE does not affect process outgrowth or differentiation of the cells, although moderate expression of NTE by expression of the NTE esterase domain accelerates the elongation of neurite processes. Mipafox, a neurotoxic organophosphate, was shown to block process outgrowth and differentiation in cells that have lowered NTE activity due to RNA interference, suggesting that mipafox may interact with other molecules to exert its effect in this context. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:30 / 38
页数:9
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