Department of Mechanical Engineering, Institute for Computational Mechanics, Technical University of Munich, Boltzmannstrasse 15, Garching 85748, Germany; Department of Mechanical Engineering, Institute of Continuum and Materials Mechanics, Hamburg University of Technology, Eissendorfer Strasse 42, Hamburg 21073, Germany.
Department of Biomedical Engineering, Yale University, 55 Prospect Street, New Haven, CT 06511.
J Biomech Eng. 2020 Jul 1;142(7). doi: 10.1115/1.4046201.
Soft biological tissues consist of cells and extracellular matrix (ECM), a network of diverse proteins, glycoproteins, and glycosaminoglycans that surround the cells. The cells actively sense the surrounding ECM and regulate its mechanical state. Cell-seeded collagen or fibrin gels, so-called tissue equivalents, are simple but powerful model systems to study this phenomenon. Nevertheless, few quantitative studies document the stresses that cells establish and maintain in such gels; moreover, most prior data were collected via uniaxial experiments whereas soft tissues are mainly subject to multiaxial loading in vivo. To begin to close this gap between existing experimental data and in vivo conditions, we describe here a computer-controlled bioreactor that enables accurate measurements of the evolution of mechanical tension and deformation of tissue equivalents under well-controlled biaxial loads. This device allows diverse studies, including how cells establish a homeostatic state of biaxial stress and if they maintain it in response to mechanical perturbations. It similarly allows, for example, studies of the impact of cell and matrix density, exogenous growth factors and cytokines, and different types of loading conditions (uniaxial, strip-biaxial, and biaxial) on these processes. As illustrative results, we show that NIH/3T3 fibroblasts establish a homeostatic mechanical state that depends on cell density and collagen concentration. Following perturbations from this homeostatic state, the cells were able to recover biaxial loading similar to homeostatic. Depending on the precise loads, however, they were not always able to fully maintain that state.
软生物组织由细胞和细胞外基质(ECM)组成,ECM 是一个由多种蛋白质、糖蛋白和糖胺聚糖组成的网络,围绕着细胞。细胞主动感知周围的 ECM,并调节其力学状态。细胞接种的胶原或纤维蛋白凝胶,即所谓的组织等效物,是研究这种现象的简单而强大的模型系统。然而,很少有定量研究记录细胞在这些凝胶中建立和维持的应力;此外,大多数先前的数据是通过单轴实验收集的,而软组织在体内主要受到多轴加载。为了开始弥合现有实验数据与体内条件之间的差距,我们在这里描述了一种计算机控制的生物反应器,该反应器能够在精确控制的双轴载荷下准确测量组织等效物的机械张力和变形的演变。该设备允许进行各种研究,包括细胞如何建立双轴应力的平衡状态,以及它们是否在响应力学扰动时保持这种状态。同样,它允许例如研究细胞和基质密度、外源性生长因子和细胞因子以及不同类型的加载条件(单轴、条带双轴和双轴)对这些过程的影响。作为说明性结果,我们表明 NIH/3T3 成纤维细胞建立了一种依赖于细胞密度和胶原浓度的平衡力学状态。在从这种平衡状态受到干扰后,细胞能够恢复类似于平衡的双轴加载。然而,取决于精确的载荷,它们并不总是能够完全维持这种状态。