Iijima Mizuki, Sato Mitsuki, Wakabayashi Hoshi, Kojima Kaori, Togashi Kanata, Oishi Shogo, Misu Takumi, Mukai Masaru, Miyajima Hiroki, Maruo Shoji, Iijima Kazutoshi
Graduate School of Engineering Science, Yokohama National University, 79-5 Tokiwadai, Hodogaya-ku, Yokohama 240-8501, Japan.
Faculty of Engineering, Yokohama National University, 79-5 Tokiwadai, Hodogaya-ku, Yokohama 240-8501, Japan.
ACS Biomater Sci Eng. 2025 May 12;11(5):2875-2887. doi: 10.1021/acsbiomaterials.4c02156. Epub 2025 Apr 18.
Various tissues have oriented collagen structures that confer mechanical strength and stability. However, creating models that precisely mimic the size and direction of these tissues remains challenging. In the present study, we developed a collagen tissue with multiscale and multidirectional controlled orientation using fluidic devices prepared using three-dimensional (3D) printing technology. Two types of fluidic channels were fabricated: a one-directional "horizontal orientation model" and vertical protrusions added to create a two-directional "vertical/horizontal orientation model". A type I collagen solution, mixed with or without cells, was introduced into the fluidic channel and gelled. As a result, in the horizontal orientation model, collagen fibrils and fibers were oriented by the flow. Both the fibroblasts and stem cells were aligned parallel to the flow along the collagen structure. In the vertical/horizontal orientation model, both the horizontal and vertical parts confirmed the orientation of collagen fibrils, fibers, and fibroblasts in both directions. Observation of the model at the nanoscale level using scanning electron microscopy (SEM) can explain the collagen orientation mechanism at the molecular and fibril levels. Prior to full gelation, collagen molecules and fibrils align parallel to the flow owing to the influence of flow and channel wall effects. This wall effect, starting from the outer channel wall, creates a gelated collagen "wall" toward the inside of the channel. Collagen fibrils aggregate into collagen fibers. In our experiments focusing on collagen contraction, the cell orientation was also described. As cells proliferate in response to the contact guidance of collagen fibrils and fiber orientation, focal adhesions and F-actin are activated and organize anisotropic traction forces that, in turn, drive cell orientation. Therefore, our method enables the customization of models with the desired tissue-specific orientations, thereby advancing future possibilities in tissue engineering.
各种组织具有定向的胶原蛋白结构,赋予其机械强度和稳定性。然而,创建精确模拟这些组织大小和方向的模型仍然具有挑战性。在本研究中,我们使用三维(3D)打印技术制备的流体装置,开发了一种具有多尺度和多方向可控取向的胶原蛋白组织。制造了两种类型的流体通道:一种单向的“水平取向模型”,并添加了垂直突起以创建双向的“垂直/水平取向模型”。将含有或不含细胞的I型胶原蛋白溶液引入流体通道并凝胶化。结果,在水平取向模型中,胶原原纤维和纤维由流动定向。成纤维细胞和干细胞均沿胶原蛋白结构与流动方向平行排列。在垂直/水平取向模型中,水平和垂直部分均证实了胶原原纤维、纤维和成纤维细胞在两个方向上的取向。使用扫描电子显微镜(SEM)在纳米尺度水平观察该模型,可以解释分子和原纤维水平的胶原蛋白取向机制。在完全凝胶化之前,由于流动和通道壁效应的影响,胶原分子和原纤维与流动方向平行排列。这种壁效应从通道外壁开始,向通道内部形成凝胶化的胶原蛋白“壁”。胶原原纤维聚集成胶原纤维。在我们关注胶原蛋白收缩的实验中,也描述了细胞取向。随着细胞响应胶原原纤维和纤维取向的接触导向而增殖,粘着斑和F-肌动蛋白被激活并组织各向异性的牵引力,进而驱动细胞取向。因此,我们的方法能够定制具有所需组织特异性取向的模型,从而推动组织工程的未来发展。