School of Bio Sciences and Technology (SBST), Vellore Institute of Technology (VIT), Vellore 632014, Tamil Nadu, India.
Centre for Biomaterials, Cellular, and Molecular Theranostics (CBCMT), Vellore Institute of Technology (VIT), Vellore 632014, Tamil Nadu, India.
Int J Mol Sci. 2023 Jan 18;24(3):1912. doi: 10.3390/ijms24031912.
The culturing of cells in the laboratory under controlled conditions has always been crucial for the advancement of scientific research. Cell-based assays have played an important role in providing simple, fast, accurate, and cost-effective methods in drug discovery, disease modeling, and tissue engineering while mitigating reliance on cost-intensive and ethically challenging animal studies. The techniques involved in culturing cells are critical as results are based on cellular response to drugs, cellular cues, external stimuli, and human physiology. In order to establish in vitro cultures, cells are either isolated from normal or diseased tissue and allowed to grow in two or three dimensions. Two-dimensional (2D) cell culture methods involve the proliferation of cells on flat rigid surfaces resulting in a monolayer culture, while in three-dimensional (3D) cell cultures, the additional dimension provides a more accurate representation of the tissue milieu. In this review, we discuss the various methods involved in the development of 3D cell culture systems emphasizing the differences between 2D and 3D systems and methods involved in the recapitulation of the organ-specific 3D microenvironment. In addition, we discuss the latest developments in 3D tissue model fabrication techniques, microfluidics-based organ-on-a-chip, and imaging as a characterization technique for 3D tissue models.
在实验室中控制条件下培养细胞一直是推进科学研究的关键。基于细胞的测定法在药物发现、疾病建模和组织工程中提供简单、快速、准确和具有成本效益的方法方面发挥了重要作用,同时减少了对昂贵且具有伦理挑战性的动物研究的依赖。培养细胞所涉及的技术至关重要,因为结果基于细胞对药物、细胞信号、外部刺激和人体生理学的反应。为了建立体外培养物,细胞要么从正常或患病组织中分离出来,并允许在二维或三维空间中生长。二维(2D)细胞培养方法涉及细胞在平坦刚性表面上的增殖,从而产生单层培养物,而在三维(3D)细胞培养中,额外的维度更准确地再现了组织环境。在这篇综述中,我们讨论了开发 3D 细胞培养系统所涉及的各种方法,重点讨论了 2D 和 3D 系统之间的差异,以及再现器官特异性 3D 微环境所涉及的方法。此外,我们还讨论了 3D 组织模型制造技术、基于微流控的器官芯片以及作为 3D 组织模型特征化技术的成像方面的最新进展。