Sakamoto Yusuke, Buchanan Rachel M, Sanchez-Adams Johannah, Guilak Farshid, Sacks Michael S
Center for Cardiovascular Simulation, Institute for Computational Engineering and Sciences, Department of Biomedical Engineering, The University of Texas at Austin, Austin, TX 78712.
Departments of Orthopaedic Surgery, Duke University Medical Center, Durham, NC 27710;Departments of Biomedical Engineering, Duke University Medical Center, Durham, NC 27710.
J Biomech Eng. 2017 Feb 1;139(2):0210071-02100713. doi: 10.1115/1.4035557.
The function of the heart valve interstitial cells (VICs) is intimately connected to heart valve tissue remodeling and repair, as well as the onset and progression of valvular pathological processes. There is yet only very limited knowledge and extant models for the complex three-dimensional VIC internal stress-bearing structures, the associated cell-level biomechanical behaviors, and how they change under varying activation levels. Importantly, VICs are known to exist and function within the highly dynamic valve tissue environment, including very high physiological loading rates. Yet we have no knowledge on how these factors affect VIC function. To this end, we extended our previous VIC computational continuum mechanics model (Sakamoto, et al., 2016, "On Intrinsic Stress Fiber Contractile Forces in Semilunar Heart Valve Interstitial Cells Using a Continuum Mixture Model," J. Mech. Behav. Biomed. Mater., 54(244-258)). to incorporate realistic stress-fiber geometries, force-length relations (Hill model for active contraction), explicit α-smooth muscle actin (α-SMA) and F-actin expression levels, and strain rate. Novel micro-indentation measurements were then performed using cytochalasin D (CytoD), variable KCl molar concentrations, both alone and with transforming growth factor β1 (TGF-β1) (which emulates certain valvular pathological processes) to explore how α-SMA and F-actin expression levels influenced stress fiber responses under quasi-static and physiological loading rates. Simulation results indicated that both F-actin and α-SMA contributed substantially to stress fiber force generation, with the highest activation state (90 mM KCL + TGF-β1) inducing the largest α-SMA levels and associated force generation. Validation was performed by comparisons to traction force microscopy studies, which showed very good agreement. Interestingly, only in the highest activation state was strain rate sensitivity observed, which was captured successfully in the simulations. These unique findings demonstrated that only VICs with high levels of αSMA expression exhibited significant viscoelastic effects. Implications of this study include greater insight into the functional role of α-SMA and F-actin in VIC stress fiber function, and the potential for strain rate-dependent effects in pathological states where high levels of α-SMA occur, which appear to be unique to the valvular cellular in vivo microenvironment.
心脏瓣膜间质细胞(VICs)的功能与心脏瓣膜组织的重塑和修复密切相关,同时也与瓣膜病理过程的发生和发展相关。然而,对于复杂的三维VIC内部应力承受结构、相关的细胞水平生物力学行为,以及它们在不同激活水平下如何变化,目前的了解还非常有限,现有的模型也很少。重要的是,已知VICs存在于高度动态的瓣膜组织环境中并在其中发挥作用,包括非常高的生理负荷率。然而,我们并不清楚这些因素如何影响VIC的功能。为此,我们扩展了之前的VIC计算连续介质力学模型(坂本等人,2016年,“使用连续介质混合模型研究半月形心脏瓣膜间质细胞中的内在应力纤维收缩力”,《生物医学材料力学行为杂志》,第54卷(第244 - 258页)),纳入了实际应力纤维几何形状、力 - 长度关系(主动收缩的希尔模型)、明确的α -平滑肌肌动蛋白(α - SMA)和F - 肌动蛋白表达水平以及应变率。然后使用细胞松弛素D(CytoD)、可变的KCl摩尔浓度,单独或与转化生长因子β1(TGF - β1)(模拟某些瓣膜病理过程)一起进行新型微压痕测量,以探索α - SMA和F - 肌动蛋白表达水平在准静态和生理负荷率下如何影响应力纤维反应。模拟结果表明,F - 肌动蛋白和α - SMA都对应力纤维力产生有很大贡献,最高激活状态(90 mM KCL + TGF - β1)诱导最高的α - SMA水平和相关力产生。通过与牵引力显微镜研究结果进行比较来进行验证,结果显示吻合度非常好。有趣的是,仅在最高激活状态下观察到应变率敏感性,并且在模拟中成功捕捉到了这一点。这些独特的发现表明只有具有高水平αSMA表达的VICs才表现出显著的粘弹性效应。这项研究的意义包括更深入了解α - SMA和F - 肌动蛋白在VIC应力纤维功能中的作用,以及在α - SMA水平较高的病理状态下应变率依赖性效应的可能性,这似乎是瓣膜细胞体内微环境所特有的。