Neural Engineering Area, The BioRobotics Institute, Scuola Superiore Sant'Anna, Pisa, Italy.
PLoS One. 2013 Aug 6;8(8):e70304. doi: 10.1371/journal.pone.0070304. Print 2013.
Recently, the effects of nanogratings have been investigated on PC12 with respect to cell polarity, neuronal differentiation, migration, maturation of focal adhesions and alignment of neurites.
METHODOLOGY/PRINCIPAL FINDINGS: A synergistic procedure was used to study the mechanism of alignment of PC12 neurites with respect to the main direction of nanogratings. Finite Element simulations were used to qualitatively assess the distribution of stresses at the interface between non-spread growth cones and filopodia, and to study their dependence on filopodial length and orientation. After modelling all adhesions under non-spread growth cone and filopodial protrusions, the values of local stress maxima resulted from the length of filopodia. Since the stress was assumed to be the main triggering cause leading to the increase and stabilization of filopodia, the position of the local maxima was directly related to the orientation of neurites. An analytic closed form equation was then written to quantitatively assess the average ridge width needed to achieve a given neuritic alignment (R(2) = 0.96), and the alignment course, when the ridge depth varied (R(2) = 0.97). A computational framework was implemented within an improved free Java environment (CX3D) and in silico simulations were carried out to reproduce and predict biological experiments. No significant differences were found between biological experiments and in silico simulations (alignment, p = 0.3571; tortuosity, p = 0.2236) with a standard level of confidence (95%).
CONCLUSIONS/SIGNIFICANCE: A mechanism involved in filopodial sensing of nanogratings is proposed and modelled through a synergistic use of FE models, theoretical equations and in silico simulations. This approach shows the importance of the neuritic terminal geometry, and the key role of the distribution of the adhesion constraints for the cell/substrate coupling process. Finally, the effects of the geometry of nanogratings were explicitly considered in cell/surface interactions thanks to the analytic framework presented in this work.
最近,人们研究了纳米光栅对 PC12 细胞极性、神经元分化、迁移、焦点黏附成熟和轴突排列的影响。
方法/主要发现:采用协同程序研究了 PC12 轴突沿纳米光栅主方向排列的机制。有限元模拟用于定性评估非扩展生长锥和丝状伪足界面处的应力分布,并研究其对丝状伪足长度和方向的依赖性。在对所有非扩展生长锥和丝状伪足下的黏附进行建模后,得到了由丝状伪足长度引起的局部最大应力值。由于假设应力是导致丝状伪足增加和稳定的主要触发因素,因此局部最大值的位置与轴突的方向直接相关。然后,写出一个解析封闭形式的方程来定量评估实现给定轴突排列所需的脊宽度(R^2=0.96),以及脊深度变化时的排列过程(R^2=0.97)。在改进的免费 Java 环境(CX3D)中实现了计算框架,并进行了计算机模拟以重现和预测生物实验。在置信水平为 95%时,生物实验和计算机模拟之间没有发现显著差异(排列,p=0.3571;扭曲,p=0.2236)。
结论/意义:通过协同使用有限元模型、理论方程和计算机模拟,提出并建模了一种丝状伪足感知纳米光栅的机制。这种方法表明了轴突末端几何形状的重要性,以及黏附约束分布对细胞/基底偶联过程的关键作用。最后,由于本工作中提出的分析框架,明确考虑了纳米光栅的几何形状对细胞/表面相互作用的影响。