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A549细胞中锌响应蛋白质组分析及MTF-1调控的蛋白质的时间依赖性表达

Zn-responsive proteome profiling and time-dependent expression of proteins regulated by MTF-1 in A549 cells.

作者信息

Zhao Wen-jie, Song Qun, Wang Yan-hong, Li Ke-jin, Mao Li, Hu Xin, Lian Hong-zhen, Zheng Wei-juan, Hua Zi-chun

机构信息

State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry & Chemical Engineering and Center of Materials Analysis, Nanjing University, Nanjing, PR China.

State Key Laboratory of Pharmaceutical Biotechnology, School of Life Science, Nanjing University, Nanjing, PR China.

出版信息

PLoS One. 2014 Aug 27;9(8):e105797. doi: 10.1371/journal.pone.0105797. eCollection 2014.

Abstract

Zinc plays a critical role in many biological processes. However, it is toxic at high concentrations and its homeostasis is strictly regulated by metal-responsive transcription factor 1 (MTF-1) together with many other proteins to protect cells against metal toxicity and oxidative stresses. In this paper, we used high-resolution two-dimensional gel electrophoresis (2DE) to profile global changes of the whole soluble proteome in human lung adenocarcinoma (A549) cells in response to exogenous zinc treatment for 24 h. Eighteen differentially expressed proteins were identified by MALDI TOF/TOF and MASCOT search. In addition, we used Western blotting and RT-PCR to examine the time-dependent changes in expression of proteins regulated by MTF-1 in response to Zn treatment, including the metal binding protein MT-1, the zinc efflux protein ZnT-1, and the zinc influx regulator ZIP-1. The results indicated that variations in their mRNA and protein levels were consistent with their functions in maintaining the homeostasis of zinc. However, the accumulation of ZIP-1 transcripts was down-regulated while the protein level was up-regulated during the same time period. This may be due to the complex regulatory mechanism of ZIP-1, which is involved in multiple signaling pathways. Maximal changes in protein abundance were observed at 10 h following Zn treatment, but only slight changes in protein or mRNA levels were observed at 24 h, which was the time-point frequently used for 2DE analyses. Therefore, further study of the time-dependent Zn-response of A549 cells would help to understand the dynamic nature of the cellular response to Zn stress. Our findings provide the basis for further study into zinc-regulated cellular signaling pathways.

摘要

锌在许多生物过程中发挥着关键作用。然而,高浓度的锌具有毒性,其体内平衡由金属反应转录因子1(MTF-1)以及许多其他蛋白质严格调控,以保护细胞免受金属毒性和氧化应激的影响。在本文中,我们使用高分辨率二维凝胶电泳(2DE)来分析人肺腺癌(A549)细胞在接受24小时外源性锌处理后全可溶性蛋白质组的整体变化。通过基质辅助激光解吸电离飞行时间质谱(MALDI TOF/TOF)和MASCOT搜索鉴定出18种差异表达的蛋白质。此外,我们使用蛋白质印迹法和逆转录-聚合酶链反应(RT-PCR)来检测MTF-1调控的蛋白质在锌处理后随时间的表达变化,包括金属结合蛋白MT-1、锌流出蛋白ZnT-1和锌流入调节因子ZIP-1。结果表明,它们的mRNA和蛋白质水平的变化与其在维持锌体内平衡中的功能一致。然而,在同一时期,ZIP-1转录本的积累下调,而蛋白质水平上调。这可能是由于ZIP-1复杂的调控机制,它参与多种信号通路。在锌处理后10小时观察到蛋白质丰度的最大变化,但在24小时仅观察到蛋白质或mRNA水平的轻微变化,而24小时是常用于2DE分析的时间点。因此,进一步研究A549细胞对锌的时间依赖性反应将有助于理解细胞对锌应激反应的动态性质。我们的发现为进一步研究锌调节的细胞信号通路提供了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d05c/4146543/07c69b3c9897/pone.0105797.g001.jpg

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