Department of Sport Medicine and Rehabilitation Center, Shanghai University of Sport, Shanghai 200438, China.
Rehabilitation Research Laboratory 2rLab, Department of Business Economics Health and Social Care, University of Applied Sciences and Arts of Southern Switzerland, 6928 Manno, Switzerland.
Int J Mol Sci. 2019 Jan 29;20(3):564. doi: 10.3390/ijms20030564.
A quantitative proteomic analysis of the response to dry needling combined with static stretching treatment was performed in a rat model of active myofascial trigger points (MTrPs). 36 rats were divided into a model group (MG), a stretching group (SG) and a dry needling combined with stretching group (SDG). We performed three biological replicates to compare large-scale differential protein expression between groups by tandem mass tag (TMT) labeling technology based on nanoscale liquid chromatography mass spectrometry analysis (LC⁻MS/MS). Hierarchical clustering, Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment and protein-protein interaction network analyses were performed for the general characterization of overall enriched proteins. For validation of the results of TMT, the candidate proteins were verified by parallel reaction monitoring (PRM) analysis. 285 differentially expressed proteins between groups were identified and quantified. Tight junction pathway played a dominant role in dry needling combined with static stretching treatment for the rat model of active MTrPs. Three candidate proteins, namely actinin alpha 3, calsequestrin-1 and parvalbumin alpha, were further validated, consistent with the results of LC⁻MS/MS. This is the first proteomics-based study to report the therapeutic mechanism underlying dry needling and static stretching treatment for MTrPs. Further functional verification of the potential signaling pathways and the enriched proteins is warranted.
采用主动肌筋膜触发点(MTrP)大鼠模型,对干针结合静态拉伸治疗的反应进行了定量蛋白质组学分析。将 36 只大鼠分为模型组(MG)、拉伸组(SG)和干针结合拉伸组(SDG)。我们通过基于纳升液相色谱-串联质谱分析(LC-MS/MS)的串联质量标签(TMT)标记技术,进行了三个生物学重复,以比较组间大规模差异蛋白表达。进行层次聚类、基因本体(GO)、京都基因与基因组百科全书(KEGG)富集和蛋白质-蛋白质相互作用网络分析,以全面描述整体富集蛋白的特征。为了验证 TMT 结果,通过平行反应监测(PRM)分析验证了候选蛋白。鉴定并定量了 285 个组间差异表达蛋白。紧密连接通路在干针结合静态拉伸治疗主动 MTrP 大鼠模型中起主导作用。进一步验证了三个候选蛋白,即肌动蛋白α 3、钙网蛋白 1 和钙结合蛋白α,其结果与 LC-MS/MS 一致。这是第一项基于蛋白质组学的研究,报告了干针和静态拉伸治疗 MTrP 的治疗机制。有必要进一步验证潜在信号通路和富集蛋白的功能。