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轴突运输蛋白质组学揭示了在损伤的坐骨神经中,翻译机器向损伤部位的迁移。

Axonal transport proteomics reveals mobilization of translation machinery to the lesion site in injured sciatic nerve.

机构信息

Department of Biological Chemistry, Weizmann Institute of Science, 76100 Rehovot, Israel.

出版信息

Mol Cell Proteomics. 2010 May;9(5):976-87. doi: 10.1074/mcp.M900369-MCP200. Epub 2009 Nov 14.

Abstract

Investigations of the molecular mechanisms underlying responses to nerve injury have highlighted the importance of axonal transport systems. To obtain a comprehensive view of the protein ensembles associated with axonal transport in injured axons, we analyzed the protein compositions of axoplasm concentrated at ligatures following crush injury of rat sciatic nerve. LC-MS/MS analyses of iTRAQ-labeled peptides from axoplasm distal and proximal to the ligation sites revealed protein ensembles transported in both anterograde and retrograde directions. Variability of replicates did not allow straightforward assignment of proteins to functional transport categories; hence, we performed principal component analysis and factor analysis with subsequent clustering to determine the most prominent injury-related transported proteins. This strategy circumvented experimental variability and allowed the extraction of biologically meaningful information from the quantitative neuroproteomics experiments. 299 proteins were highlighted by principal component analysis and factor analysis, 145 of which correlate with retrograde and 154 of which correlate with anterograde transport after injury. The analyses reveal extensive changes in both anterograde and retrograde transport proteomes in injured peripheral axons and emphasize the importance of RNA binding and translational machineries in the axonal response to injury.

摘要

对神经损伤反应背后的分子机制的研究强调了轴突运输系统的重要性。为了全面了解损伤轴突中与轴突运输相关的蛋白质复合物,我们分析了在大鼠坐骨神经挤压伤后结扎处浓缩的轴浆中的蛋白质组成。来自结扎部位远端和近端轴浆的 iTRAQ 标记肽的 LC-MS/MS 分析揭示了顺行和逆行运输的蛋白质复合物。由于重复的可变性不允许将蛋白质直接分配到功能运输类别中;因此,我们进行了主成分分析和因子分析,随后进行聚类,以确定最突出的与损伤相关的运输蛋白。这种策略避免了实验变异性,并从定量神经蛋白质组学实验中提取了有生物学意义的信息。主成分分析和因子分析突出了 299 种蛋白质,其中 145 种与逆行运输相关,154 种与损伤后的顺行运输相关。这些分析揭示了损伤外周轴突中顺行和逆行运输蛋白质组的广泛变化,并强调了 RNA 结合和翻译机制在轴突对损伤的反应中的重要性。

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