Huelter-Hassler Diana, Tomakidi Pascal, Steinberg Thorsten, Jung Britta A
Department of Orthodontics, University Medical Center Freiburg, Germany.
Faculty of Biology, University of Freiburg, Germany.
Eur J Orthod. 2017 Jun 1;39(3):251-257. doi: 10.1093/ejo/cjx012.
During orthodontic tooth movement (OTM), human periodontal ligament fibroblasts (hPDLFs) sense, and respond to mechanical forces. Since the molecular constituents involved in these processes are not fully elucidated, the objective of the present study was to identify further key molecules of the cellular strain response.
Primary hPDLFs were strained with a static equiaxial strain of 2.5 per cent for 15 minutes, 1 hour, 6 hours, and 24 hours. Western blot (WB) and indirect immunofluorescence (IIF) analyses were performed to investigate the quantity and activation state of proteins involved in mechanotransduction, namely extracellular signal-regulated kinase (ERK) 1/2 and yes-associated protein (YAP). On the cell behavioural level, proliferation was assessed by the marker of proliferation KI-67.
In response to the applied strain, an early decline of phosphorylated and thus activated ERK1/2 was observed, followed by a mild recovery. Furthermore, both WB and IIF analyses revealed a modulation of nuclear YAP localisation. Concomitant with the modulation of YAP, the applied strain evoked an early increase in nuclear KI-67 amount, followed by a continuous decrease.
Consecutive studies will focus on scrutinising the suggested relationship between YAP and proliferation in response to static strain.
Our findings provide evidence of ERK1/2 and YAP being biomechanically responsive molecular players in the context of OTM, among which YAP rather than ERK1/2 seems to be mechanistically interrelated with proliferation. Furthermore, the molecular and cell behavioural strain-induced early modulations may point to an involvement of the investigated molecules in the initial and the following lag phase of OTM.
在正畸牙齿移动(OTM)过程中,人牙周膜成纤维细胞(hPDLFs)感知并响应机械力。由于参与这些过程的分子成分尚未完全阐明,本研究的目的是进一步确定细胞应变反应的关键分子。
将原代hPDLFs用2.5%的静态等轴应变拉伸15分钟、1小时、6小时和24小时。进行蛋白质免疫印迹(WB)和间接免疫荧光(IIF)分析,以研究参与机械转导的蛋白质,即细胞外信号调节激酶(ERK)1/2和Yes相关蛋白(YAP)的数量和激活状态。在细胞行为水平上,通过增殖标志物KI-67评估增殖情况。
响应施加的应变,观察到磷酸化并因此被激活的ERK1/2早期下降,随后有轻微恢复。此外,WB和IIF分析均显示核YAP定位发生了变化。与YAP的变化同时,施加的应变引起核KI-67量早期增加,随后持续下降。
后续研究将集中于仔细研究YAP与静态应变响应中增殖之间的推测关系。
我们的研究结果证明ERK1/2和YAP在OTM背景下是生物力学响应分子,其中YAP而非ERK1/2似乎在机制上与增殖相关。此外,分子和细胞行为的应变诱导早期调节可能表明所研究的分子参与了OTM的初始阶段和随后的滞后阶段。