Shahin-Shamsabadi A, Selvaganapathy P R
School of Biomedical Engineering, McMaster University, Canada.
Department of Mechanical Engineering, McMaster University, Canada.
Mater Today Bio. 2020 Jul 28;7:100070. doi: 10.1016/j.mtbio.2020.100070. eCollection 2020 Jun.
Three-dimensional (3D) tissue models are superior to two-dimensional (2D) cell cultures in replicating natural physiological/pathological conditions by recreating the cellular and cell-matrix interactions more faithfully. Nevertheless, current 3D models lack either the rich multicellular environment or fail to provide appropriate biophysical stimuli both of which are required to properly recapitulate the dynamic microenvironment of tissues and organs. Here, we describe the rapid construction of multicellular, tubular tissue constructs termed Tissue-in-a-Tube using self-assembly process in tubular molds with the ability to incorporate a variety of biophysical stimuli such as electrical field, mechanical deformation, and shear force of the fluid flow. Unlike other approaches, this method is simple, requires only oxygen permeable silicone tubing that molds the tissue construct and thin stainless-steel pins inserted in it to anchor the construct and could be used to provide electrical and mechanical stimuli, simultaneously. The annular region between the tissue construct and the tubing is used for perfusion. Highly stable, macroscale, and robust constructs anchored to the pins form as a result of self-assembly of the extracellular matrix (ECM) and cells in the bioink that is filled into the tubing. We demonstrate patterning of grafts containing cell types in the constructs in axial and radial modes with clear interface and continuity between the layers. Different environmental factors affecting cell behavior such as compactness of the structure and size of the constructs can be controlled through parameters such as initial cell density, ECM content, tubing size, as well as the distance between anchor pins. Using connectors, network of tubing can be assembled to create complex macrostructured tissues (centimeters length) such as fibers that are bifurcated or columns with different axial thicknesses which can then be used as building blocks for biomimetic constructs or tissue regeneration. The method is versatile and compatible with various cell types including endothelial, epithelial, skeletal muscle cells, osteoblast cells, and neuronal cells. As an example, long mature skeletal muscle and neuronal fibers as well as bone constructs were fabricated with cellular alignment dictated by the applied electrical field. The versatility, speed, and low cost of this method is suited for widespread application in tissue engineering and regenerative medicine.
三维(3D)组织模型在更忠实地重现细胞与细胞外基质相互作用从而复制自然生理/病理条件方面优于二维(2D)细胞培养。然而,当前的3D模型要么缺乏丰富的多细胞环境,要么无法提供适当的生物物理刺激,而这两者都是正确概括组织和器官动态微环境所必需的。在此,我们描述了一种称为“管中组织”的多细胞管状组织构建体的快速构建方法,该方法利用管状模具中的自组装过程,能够纳入多种生物物理刺激,如电场、机械变形和流体流动的剪切力。与其他方法不同,此方法简单,仅需可透氧的硅胶管来塑造组织构建体以及插入其中的细不锈钢销来固定构建体,并且可用于同时提供电刺激和机械刺激。组织构建体与管子之间的环形区域用于灌注。由于填充到管子中的生物墨水内细胞外基质(ECM)和细胞的自组装,形成了高度稳定、宏观且坚固的固定在销上的构建体。我们展示了构建体中包含不同细胞类型的移植物在轴向和径向模式下的图案化,各层之间具有清晰的界面和连续性。通过诸如初始细胞密度、ECM含量、管子尺寸以及固定销之间的距离等参数,可以控制影响细胞行为的不同环境因素,如结构的致密性和构建体的大小。使用连接器,可以组装管网络以创建复杂的宏观结构组织(厘米级长度),如分叉的纤维或具有不同轴向厚度的柱体,然后可将其用作仿生构建体或组织再生的构建模块。该方法具有通用性,与包括内皮细胞、上皮细胞、骨骼肌细胞、成骨细胞和神经元细胞在内的各种细胞类型兼容。例如,利用施加的电场控制细胞排列,制造出了长的成熟骨骼肌和神经元纤维以及骨构建体。此方法的通用性、速度和低成本适合在组织工程和再生医学中广泛应用。