Foolen Jasper, Janssen-van den Broek Marloes W J T, Baaijens Frank P T
Department of Biomedical Engineering, Eindhoven University of Technology, PO Box 513, GEM-Z 4.117, 5600 MB Eindhoven, The Netherlands.
Department of Biomedical Engineering, Eindhoven University of Technology, PO Box 513, GEM-Z 4.117, 5600 MB Eindhoven, The Netherlands.
Acta Biomater. 2014 May;10(5):1876-85. doi: 10.1016/j.actbio.2013.12.001. Epub 2013 Dec 12.
Cells adapt in response to mechanical stimulation to ensure adequate tissue functioning. F-actin stress fibers provide a key element in the adaptation process. The high sensitivity and fast adaptation of the F-actin cytoskeleton to cyclic strain have been studied extensively in a 2-D environment; however, 3-D data are scarce. Our previous work showed that stress fibers organize perpendicular to cyclic stretching (stretch-avoidance) in three dimensions. However, stretch-avoidance was absent when cells populated a high density matrix. In this study our aim was to obtain more insight into the synergy between matrix density and the signaling pathways that govern stress fiber remodeling. Therefore we studied stress fiber organization in 3-D reconstituted collagen tissues (at low and high matrix density), subjected to cyclic stretch upon interference with molecular signaling pathways. In particular, the influence of the small GTPase Rho and its downstream effectors were studied. Only at low matrix density does stress fiber stretch avoidance show a stretch-magnitude-dependent response. The activity of matrix metalloproteinases (MMPs), Rho-kinase and myosin light chain kinase are essential for stress fiber reorientation. Although high matrix density restricts stress fiber reorientation, Rho activation can overcome this restriction, but only in the presence of active MMPs. Results from this study highlight a synergistic action between matrix remodeling and Rho signaling in cyclic-stretch-induced stress fiber organization in 3-D tissue.
细胞会对机械刺激做出适应性反应,以确保组织功能正常。F-肌动蛋白应力纤维在这一适应过程中起着关键作用。F-肌动蛋白细胞骨架对周期性应变的高敏感性和快速适应性已在二维环境中得到广泛研究;然而,三维数据却很匮乏。我们之前的研究表明,应力纤维在三维空间中垂直于周期性拉伸方向排列(拉伸回避)。然而,当细胞处于高密度基质中时,拉伸回避现象消失。在本研究中,我们的目的是更深入地了解基质密度与调控应力纤维重塑的信号通路之间的协同作用。因此,我们研究了在干扰分子信号通路后,三维重组胶原组织(低基质密度和高基质密度)中应力纤维的排列情况,该组织受到周期性拉伸。特别研究了小GTP酶Rho及其下游效应器的影响。只有在低基质密度下,应力纤维的拉伸回避才表现出与拉伸幅度相关的反应。基质金属蛋白酶(MMPs)、Rho激酶和肌球蛋白轻链激酶的活性对于应力纤维的重新定向至关重要。尽管高基质密度会限制应力纤维的重新定向,但Rho激活可以克服这种限制,但前提是存在活性MMPs。本研究结果突出了基质重塑与Rho信号在三维组织中周期性拉伸诱导的应力纤维组织形成过程中的协同作用。