Caddeo Silvia, Boffito Monica, Sartori Susanna
Department of Mechanical and Aerospace Engineering, Politecnico di Torino, Turin, Italy.
Department of Oral Cell Biology, Academic Center for Dentistry Amsterdam, Amsterdam, Netherlands.
Front Bioeng Biotechnol. 2017 Jul 26;5:40. doi: 10.3389/fbioe.2017.00040. eCollection 2017.
In the tissue engineering (TE) paradigm, engineering and life sciences tools are combined to develop bioartificial substitutes for organs and tissues, which can in turn be applied in regenerative medicine, pharmaceutical, diagnostic, and basic research to elucidate fundamental aspects of cell functions or to identify mechanisms involved in aging processes and disease onset and progression. The complex three-dimensional (3D) microenvironment in which cells are organized allows the interaction between different cell types and between cells and the extracellular matrix, the composition of which varies as a function of the tissue, the degree of maturation, and health conditions. In this context, 3D models can more realistically reproduce a tissue or organ than two-dimensional (2D) models. Moreover, they can overcome the limitations of animal models and reduce the need for tests, according to the "3Rs" guiding principles for a more ethical research. The design of 3D engineered tissue models is currently in its development stage, showing high potential in overcoming the limitations of already available models. However, many issues are still opened, concerning the identification of the optimal scaffold-forming materials, cell source and biofabrication technology, and the best cell culture conditions (biochemical and physical cues) to finely replicate the native tissue and the surrounding environment. In the near future, 3D tissue-engineered models are expected to become useful tools in the preliminary testing and screening of drugs and therapies and in the investigation of the molecular mechanisms underpinning disease onset and progression. In this review, the application of TE principles to the design of 3D models will be surveyed, with a focus on the strengths and weaknesses of this emerging approach. In addition, a brief overview on the development of models of healthy and pathological bone, heart, pancreas, and liver will be presented.
在组织工程(TE)范式中,工程学和生命科学工具相结合,以开发用于器官和组织的生物人工替代物,这些替代物可反过来应用于再生医学、制药、诊断和基础研究,以阐明细胞功能的基本方面,或识别衰老过程以及疾病发生和发展所涉及的机制。细胞所处的复杂三维(3D)微环境允许不同细胞类型之间以及细胞与细胞外基质之间相互作用,细胞外基质的组成随组织、成熟程度和健康状况而变化。在这种情况下,3D模型比二维(2D)模型能更真实地再现组织或器官。此外,根据更具伦理的研究的“3R”指导原则,它们可以克服动物模型的局限性并减少试验需求。3D工程组织模型的设计目前正处于发展阶段,在克服现有模型的局限性方面显示出巨大潜力。然而,许多问题仍然存在,涉及最佳支架形成材料、细胞来源和生物制造技术的识别,以及最佳细胞培养条件(生化和物理线索),以精细复制天然组织及其周围环境。在不久的将来,3D组织工程模型有望成为药物和疗法初步测试和筛选以及疾病发生和发展背后分子机制研究的有用工具。在这篇综述中,将探讨TE原理在3D模型设计中的应用,重点关注这种新兴方法的优缺点。此外,还将简要概述健康和病理状态下的骨、心脏、胰腺和肝脏模型的发展情况。