Zhang Yimei, Kou Xiaoxing, Jiang Nan, Liu Yan, Tay Franklin R, Zhou Yanheng
The Department of Orthodontics, Peking University School and Hospital of Stomatology, Beijing, China.
The Center of Laboratory, Peking University School and Hospital of Stomatology, Beijing, China.
J Dent. 2017 Feb;57:57-65. doi: 10.1016/j.jdent.2016.12.007. Epub 2016 Dec 12.
Malocclusion may be corrected nonsurgically by mechanical tooth movement. The plasma protein profiles of human subjects receiving the first phase of orthodontic treatment were examined to test the hypothesis that application of mechanical stresses to teeth induces systemic proteomic alterations.
Tandem mass tag-based liquid chromatography-mass spectrometry (LC-MS/MS) was used to examine systemic proteomic alterations in subjects undergoing controlled stress application (N=10) and in volunteers not receiving treatment (N=7) at 3 time intervals within 24h. Proteins differentially expressed by the tooth movement group were functionally analyzed with "Gene Ontology" (GO) and "Search Tool to Retrieve Interacting Genes/proteins" (STRING) softwares. Enzyme-Linked Immunosorbent Assay and Western-blot were used to validate the in vivo protein alterations. An in vitro model consisting of human periodontal ligament cells (hPDLCs) under compression was used to validate the force-responsive characteristics of galectin-3 binding protein (LGALS3BP).
Sixteen out of the 294 proteins identified by LC-MS/MS were differentially expressed in the plasma of subjects receiving controlled mechanical stresses for moving teeth. Those proteins were clustered in biological processes related to acute inflammatory response and vesicle-related transportation. Serotransferrin, fibronectin and LGALS3BP were processed for confirmation in vivo; LGALS3BP was significantly increased in the tooth movement group. In vitro secretion of LGALS3BP in PDLCs was force-responsive.
Regional application of mechanical stresses stimulates systemic proteomic changes. Because serum LGALS3BP is over-expressed in different systemic diseases, including cancer, further work is needed to examine how systemic up-regulation of LGALS3BP affects the progression of those diseases.
错牙合畸形可通过机械性牙齿移动进行非手术矫正。对接受正畸治疗第一阶段的人类受试者的血浆蛋白质谱进行检测,以验证对牙齿施加机械应力会引起全身蛋白质组学改变这一假设。
采用基于串联质量标签的液相色谱 - 质谱联用技术(LC-MS/MS),在24小时内的3个时间间隔,检测接受控制性应力施加的受试者(N = 10)和未接受治疗的志愿者(N = 7)的全身蛋白质组学变化。利用“基因本体论”(GO)和“检索相互作用基因/蛋白质的搜索工具”(STRING)软件,对牙齿移动组中差异表达的蛋白质进行功能分析。采用酶联免疫吸附测定法和蛋白质印迹法验证体内蛋白质的变化。使用由受压的人牙周膜细胞(hPDLCs)组成的体外模型,验证半乳糖凝集素 - 3结合蛋白(LGALS3BP)的力反应特性。
LC-MS/MS鉴定出的294种蛋白质中,有16种在接受控制性牙齿移动机械应力的受试者血浆中差异表达。这些蛋白质聚集在与急性炎症反应和囊泡相关运输有关的生物学过程中。对血清转铁蛋白、纤连蛋白和LGALS3BP进行体内验证;牙齿移动组中LGALS3BP显著增加。PDLCs中LGALS3BP的体外分泌具有力反应性。
局部施加机械应力会刺激全身蛋白质组学变化。由于血清LGALS3BP在包括癌症在内的不同全身性疾病中过度表达,因此需要进一步研究LGALS3BP的全身上调如何影响这些疾病的进展。