瞬时转染金属硫蛋白-3基因诱导SH-SY5Y神经母细胞瘤细胞系差异蛋白表达。

Bo Zhou, Wei Yang, Jian-Guo Ji, Bing-Gen Ru
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摘要

金属硫蛋白-3(MT-3)又称生长抑制因子(GIF),主要表达于中枢神经系统(CNS)。它属于金属硫蛋白(MT)家族,但具有MT-1/MT-2等其他家族成员所不具有的一些独特性质。近年来,MT-3被认为是一种多用途蛋白,除了MT-3的共同作用外,还可能在中枢神经系统中发挥重要的神经调节和神经保护作用,但MT-3的主要功能及其多种功能的机制尚未阐明。本研究以人神经母细胞瘤细胞系SH-SY5Y为研究对象,基于比较蛋白质组学分析,研究瞬时转染MT-3基因对细胞整体蛋白的影响。在一个2D凝胶中,考马塞染色平均显示约750个斑点,其中17个蛋白质通过ImageMaster 2D Elite软件进行半定量分析显示出显着和可重复的变化。其中12个蛋白上调,5个蛋白下调。利用基质辅助激光解吸/电离飞行时间质谱技术,进一步鉴定出锌指蛋白、谷氨酸转运蛋白、增强蛋白等10个蛋白,它们参与中枢神经系统功能调节的几个重要通路。结果表明,MT-3可能通过调控这些蛋白的表达来发挥其独特的功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differential protein expression induced by transient transfection of metallothionein-3 gene in SH-SY5Y neuroblastoma cell line.

Metallothionein-3(MT-3), also known as growth inhibitory factor (GIF), is predominantly expressed in central nervous system (CNS). It belongs to the family of metallothionein(MT) but has several unique properties that are not shared by other family members such as MT-1/MT-2. In the past few years, MT-3 had been postulated to be a multipurpose protein which could play important neuromodulatory and neuroprotective roles in CNS besides the common roles of MTs. However, the primary function of MT-3 and the mechanism underlying its multiple functions were not elucidated so far. In present study, human neuroblastoma cell line SH-SY5Y was employed to study the overall cellular protein changes induced by transient transfection of MT-3 gene, based on comparative proteome analysis. Averagely about 750 spots were visualized by Coomassie staining in one 2D gel, in which 17 proteins were shown to display significant and reproducible changes by semiquantitative analysis with ImageMaster 2D Elite software. Among them, 12 proteins were up-regulated while other 5 proteins were down-regulated. Using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry, 10 proteins were further identified to be zinc finger protein, glutamate transporter, and enhancer protein, etc., which were involved in several important pathways regulating the functions of central nervous system. The results showed that MT-3 might exert its unique functions by regulating the expression of these proteins.

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