From the ‡Center for Aging and Regeneration, Millennium Nucleus in Regenerative Biology, Faculty of Biological Sciences, P. Universidad Católica de Chile, Alameda 340, Santiago, Chile.
§Department of Chemistry, Michigan State University, East Lansing, Michigan 48824.
Mol Cell Proteomics. 2018 Apr;17(4):592-606. doi: 10.1074/mcp.RA117.000215. Epub 2018 Jan 22.
The capacity to regenerate the spinal cord after an injury is a coveted trait that only a limited group of nonmammalian organisms can achieve. In , this capacity is only present during larval or tadpole stages, but is absent during postmetamorphic frog stages. This provides an excellent model for comparative studies between a regenerative and a nonregenerative stage to identify the cellular and molecular mechanisms that explain this difference in regenerative potential. Here, we used iTRAQ chemistry to obtain a quantitative proteome of the spinal cord 1 day after a transection injury in regenerative and nonregenerative stage animals, and used sham operated animals as controls. We quantified a total of 6,384 proteins, with 172 showing significant differential expression in the regenerative stage and 240 in the nonregenerative stage, with an overlap of only 14 proteins. Functional enrichment analysis revealed that although the regenerative stage downregulated synapse/vesicle and mitochondrial proteins, the nonregenerative stage upregulated lipid metabolism proteins, and downregulated ribosomal and translation control proteins. Furthermore, STRING network analysis showed that proteins belonging to these groups are highly interconnected, providing interesting candidates for future functional studies. Data are available via ProteomeXchange with identifier PXD006993.
在受伤后能够再生脊髓是一种令人向往的特性,只有有限的非哺乳动物能够实现。在 ,这种能力仅存在于幼虫或蝌蚪阶段,而在变态后的青蛙阶段则不存在。这为比较研究再生和非再生阶段之间的差异提供了一个极好的模型,以确定解释这种再生潜力差异的细胞和分子机制。在这里,我们使用 iTRAQ 化学方法获得了再生和非再生阶段动物在横断损伤后 1 天的脊髓定量蛋白质组学图谱,并将假手术动物作为对照。我们总共定量了 6384 种蛋白质,其中 172 种在再生阶段有显著差异表达,240 种在非再生阶段有显著差异表达,只有 14 种蛋白质重叠。功能富集分析表明,尽管再生阶段下调了突触/囊泡和线粒体蛋白,但非再生阶段上调了脂质代谢蛋白,并下调了核糖体和翻译控制蛋白。此外,STRING 网络分析表明,属于这些组的蛋白质高度相互关联,为未来的功能研究提供了有趣的候选物。数据可通过 ProteomeXchange 以标识符 PXD006993 获得。