Zemmyo Daiki, Yamamoto Masashi, Miyata Shogo
Graduate School of Science and Technology, Keio University, 3-14-1 Hiyoshi, Yokohama 223-8522, Japan.
Department of Mechanical Engineering, Faculty of Science and Technology, Keio University, 3-14-1 Hiyoshi, Yokohama 223-8522, Japan.
Micromachines (Basel). 2021 Nov 30;12(12):1486. doi: 10.3390/mi12121486.
Decellularized tissues are considered superior scaffolds for cell cultures, preserving the microstructure of native tissues and delivering many kinds of cytokines. High hydrostatic pressure (HHP) treatment could remove cells physically from biological tissues rather than chemical methods. However, there are some risks of inducing destruction or denaturation of extracellular matrices (ECMs) at an ultrahigh level of HHP. Therefore, efficient decellularization using moderate HHP is required to remove almost all cells simultaneously to suppress tissue damage. In this study, we proposed a novel decellularization method using a moderate HHP with supercooling pretreatment. To validate the decellularization method, a supercooling device was developed to incubate human dermal fibroblasts or collagen gels in a supercooled state. The cell suspension and collagen gels were subjected to 100, 150, and 200 MPa of HHP after supercooling pretreatment, respectively. After applying HHP, the viability and morphology of the cells and the collagen network structure of the gels were evaluated. The viability of cells decreased dramatically after HHP application with supercooling pretreatment, whereas the microstructures of collagen gels were preserved and cell adhesivity was retained after HHP application. In conclusion, it was revealed that supercooling pretreatment promoted the denaturation of the cell membrane to improve the efficacy of decellularization using static application of moderate HHP. Furthermore, it was demonstrated that the HHP with supercooling pretreatment did not degenerate and damage the microstructure in collagen gels.
去细胞组织被认为是细胞培养的优质支架,可保留天然组织的微观结构并释放多种细胞因子。高静水压(HHP)处理可通过物理方式而非化学方法从生物组织中去除细胞。然而,在超高HHP水平下存在诱导细胞外基质(ECM)破坏或变性的风险。因此,需要使用适度HHP进行高效去细胞处理,以几乎同时去除所有细胞,从而抑制组织损伤。在本研究中,我们提出了一种使用适度HHP并结合过冷预处理的新型去细胞方法。为验证该去细胞方法,开发了一种过冷装置,用于在过冷状态下孵育人皮肤成纤维细胞或胶原蛋白凝胶。细胞悬液和胶原蛋白凝胶在过冷预处理后分别承受100、150和200 MPa的HHP。施加HHP后,评估细胞的活力和形态以及凝胶的胶原网络结构。过冷预处理后施加HHP,细胞活力显著下降,而胶原蛋白凝胶的微观结构得以保留,且施加HHP后细胞粘附性得以维持。总之,研究表明过冷预处理促进细胞膜变性,从而提高使用静态适度HHP进行去细胞处理的效果。此外,还证明了过冷预处理的HHP不会使胶原蛋白凝胶中的微观结构变性和受损。