Alkaya Damla, Gurcan Cansu, Kilic Pelin, Yilmazer Acelya, Gurman Gunhan
1Ankara University Stem Cell Institute, Cevizlidere Mah., Ceyhun Atuf Kansu Cd. No: 169, Balgat, 06520 Ankara, Turkey.
2Department of Biomedical Engineering, Ankara University School of Engineering, Ankara, Turkey.
3 Biotech. 2020 Apr;10(4):161. doi: 10.1007/s13205-020-2134-5. Epub 2020 Mar 6.
Lately, cellular-based cartilage joint therapies have gradually gained more attention, which leads to next generation bioengineering approaches in the development of cell-based medicinal products for human use in cartilage repair. The greatest hurdles of chondrocyte-based cartilage bioengineering are: (i) preferring the cell source; (ii) differentiation and expansion processes; (iii) the time necessary for chondrocyte expansion pre-implantation; and (iv) fixing the chondrocyte count in accordance with the lesion surface area of the patient in question. The chondrocyte presents itself to be the focal starting material for research and development of bioengineered cartilage-based medicinal products which promise the regeneration and restoration of non-orthopedic cartilage joint defects. Even though chondrocytes seem to be the first choice, inevitable complications related to proliferation, dedifferentation and redifferentiation are probable. Detailed studies are a necessity to fully investigate detailed culturing conditions, the chondrogenic strains of well-defined phenotypes and evaluation of the methods to be used in biomaterial production. Despite a majority of the current methods which aid amelioration of joint functionality, they are insufficient in fully restoring the natural structure and composition of the joint cartilage. Hence current studies have trended towards gene therapy, mesenchymal stem cells and tissue engineering practices. There are many studies addressing the outcomes of chondrocytes in the clinical scene, and many vital biomaterials have been developed for structuring the bioengineered cartilage. This study aims to convey to the audience the practical significance of chondrocyte-based clinical applications.
近来,基于细胞的软骨关节疗法逐渐受到更多关注,这促使在开发用于人类软骨修复的细胞基药用产品时采用新一代生物工程方法。基于软骨细胞的软骨生物工程面临的最大障碍包括:(i)选择细胞来源;(ii)分化和扩增过程;(iii)植入前软骨细胞扩增所需的时间;以及(iv)根据相关患者的损伤表面积确定软骨细胞数量。软骨细胞是基于生物工程软骨的药用产品研发的关键起始材料,有望实现非整形外科软骨关节缺损的再生和修复。尽管软骨细胞似乎是首选,但与增殖、去分化和再分化相关的不可避免的并发症仍有可能发生。有必要进行详细研究,以全面调查详细的培养条件、明确表型的软骨生成菌株以及生物材料生产中使用的方法的评估。尽管目前的大多数方法有助于改善关节功能,但它们在完全恢复关节软骨的自然结构和组成方面仍存在不足。因此,目前的研究趋势已转向基因治疗、间充质干细胞和组织工程实践。有许多研究探讨了软骨细胞在临床中的应用结果,并且已经开发出许多重要的生物材料用于构建生物工程软骨。本研究旨在向读者传达基于软骨细胞的临床应用的实际意义。