Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2020 Apr;10(4):161.
doi: 10.1007/s13205-020-2134-5. Epub 2020 Mar 6.

Where is human-based cellular pharmaceutical R&D taking us in cartilage regeneration?

Affiliations
Review

Where is human-based cellular pharmaceutical R&D taking us in cartilage regeneration?

Damla Alkaya et al. 3 Biotech. 2020 Apr.

Abstract

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.

Keywords: Autologous chondrocyte implantation; Cartilage bioengineering; Cartilage isolation; Chondrocyte; Chondrocyte characterization; Chondrocyte isolation.

PubMed Disclaimer

Conflict of interest statement

Conflict of interestThe authors have no conflicts of interest to declare. This research did not receive any specific grant from funding agencies in the public, commercial, or not-for profit sectors. Pelin Kilic, Damla Alkaya and Cansu Grucan performed the literature search and data analysis, and all authors had the idea for the article and thereafter drafted and critically revised the work.

Figures

Fig. 1
Fig. 1
Different cell sources with the ability to differentiate into chondrocytes
Fig. 2
Fig. 2
Combined strategies including biomolecules and scaffolds

References

    1. Adkisson HD, Milliman C, Zhang X, Mauch K, Maziarz RT, Streeter PR. Immune evasion by neocartilage-derived chondrocytes: implications for biologic repair of joint articular cartilage. Stem Cell Res. 2010;4(1):57–68. doi: 10.1016/j.scr.2009.09.004. - DOI - PubMed
    1. Amini AR, Laurencin CT, Nukavarapu SP. Bone tissue engineering: recent advances and challenges. Crit Rev Biomed Eng. 2012;40(5):363–408. doi: 10.1615/critrevbiomedeng.v40.i5.10. - DOI - PMC - PubMed
    1. Angele P, Kujat R, Nerlich M, Yoo J, Goldberg V, Johnstone B. Engineering of osteochondral tissue with bone marrow mesenchymal progenitor cells in a derivatized hyaluronan-gelatin composite sponge. Tissue Eng. 1999;5(6):545–554. doi: 10.1089/ten.1999.5.545. - DOI - PubMed
    1. Arakaki K, Kitamura N, Fujiki H, Kurokawa T, Iwamoto M, Ueno M, Kanaya F, Osada Y, Gong JP, Yasuda K. Artificial cartilage made from a novel double-network hydrogel: in vivo effects on the normal cartilage and ex vivo evaluation of the friction property. J Biomed Mater Res A. 2010;93(3):1160–1168. doi: 10.1002/jbm.a.32613. - DOI - PubMed
    1. Archer CW, Francis-West P. The chondrocyte. Int J Biochem Cell Biol. 2003;35(4):401–404. doi: 10.1016/s1357-2725(02)00301-1. - DOI - PubMed

LinkOut - more resources