Turku Bioscience Centre, University of Turku and Åbo Akademi University, FIN-20520 Turku, Finland.
Turku Bioscience Centre, University of Turku and Åbo Akademi University, FIN-20520 Turku, Finland
J Cell Sci. 2020 Jun 22;133(12):jcs242909. doi: 10.1242/jcs.242909.
Fibrillar adhesions are important structural and adhesive components in fibroblasts, and are required for fibronectin fibrillogenesis. While nascent and focal adhesions are known to respond to mechanical cues, the mechanoresponsive nature of fibrillar adhesions remains unclear. Here, we used ratiometric analysis of paired adhesion components to determine an appropriate fibrillar adhesion marker. We found that active α5β1-integrin exhibits the most definitive fibrillar adhesion localization compared to other proteins, such as tensin-1, reported to be in fibrillar adhesions. To elucidate the mechanoresponsiveness of fibrillar adhesions, we designed a cost-effective and reproducible technique to fabricate physiologically relevant stiffness gradients on thin polyacrylamide (PA) hydrogels, embedded with fluorescently labelled beads. We generated a correlation curve between bead density and hydrogel stiffness, thus enabling a readout of stiffness without the need for specialized knowhow, such as atomic force microscopy (AFM). We find that stiffness promotes growth of fibrillar adhesions in a tensin-1-dependent manner. Thus, the formation of these extracellular matrix-depositing structures is coupled to the mechanical parameters of the cell environment and may enable cells to fine-tune their matrix environment in response to changing physical conditions.
纤维状黏附是成纤维细胞中重要的结构和黏附组成部分,是纤维连接蛋白纤维形成所必需的。虽然已知原纤维黏附和焦点黏附对机械刺激有反应,但纤维状黏附的力学响应特性尚不清楚。在这里,我们使用配对黏附成分的比率分析来确定适当的纤维状黏附标记物。我们发现,与其他被报道存在于纤维状黏附中的蛋白质(如 ten-sin-1)相比,活性α5β1 整联蛋白表现出最明确的纤维状黏附定位。为了阐明纤维状黏附的力学响应性,我们设计了一种经济高效且可重复的技术,在嵌入荧光标记珠的薄聚丙烯酰胺(PA)水凝胶上制造生理相关的刚度梯度。我们生成了珠密度与水凝胶刚度之间的相关曲线,从而无需专门的专业知识(如原子力显微镜(AFM))即可实现刚度的读数。我们发现,刚度以 ten-sin-1 依赖的方式促进纤维状黏附的生长。因此,这些细胞外基质沉积结构的形成与细胞环境的力学参数相关联,并且可能使细胞能够根据物理条件的变化精细调节其基质环境。