Dual functional construct containing kartogenin releasing microtissues and curcumin for cartilage regeneration

Stem Cell Research & Therapy

Negin Asgari¹  Fatemeh Bagheri²  Mohammad Hossein Ghanian³  Amir Mohammad Ghafari³  Mohamadreza Baghaban Eslaminejad⁴  Forogh Azam Sayahpour⁴ 

[1] Department of Biomedical Engineering, Faculty of Chemical Engineering, Tarbiat Modares University;Department of Biotechnology, Faculty of Chemical Engineering, Tarbiat Modares University;Department of Cell Engineering, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR;Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR;

关键词: Cell aggregates;    Microparticles;    Kartogenin;    Curcumin;    Cartilage tissue engineering;   

DOI  :  10.1186/s13287-020-01797-2

来源: DOAJ

【 摘 要 】

Abstract Background Regeneration of articular cartilage poses a tremendous challenge due to its limited self-repair capability and inflammation at the damaged site. To generate the desired structures that mimic the structure of native tissue, microtissues with repeated functional units such as cell aggregates have been developed. Multicellular aggregates of mesenchymal stem cells (MSCs) can be used as microscale building blocks of cartilage due to their potential for cell-cell contact, cell proliferation, and differentiation. Methods Chondrogenic microtissues were developed through incorporation of kartogenin-releasing poly (lactic-co-glycolic acid) (PLGA) microparticles (KGN-MP) within the MSC aggregates. The chondrogenic potential of KGN-MP treated MSC aggregates was proven in vitro by studying the chondrogenic markers at the RNA level and histological analysis. In order to address the inflammatory responses at the defect site, the microtissues were delivered in vivo via an injectable, anti-inflammatory hydrogel that contained gelatin methacryloyl (GelMA) loaded with curcumin (Cur). Results The KGN-MPs were fabricated to support MSCs during cartilage differentiation. According to real-time RT-PCR analysis, the presence of KGN in the aggregates led to the expression of cartilage markers by the MSCs. Both toluidine blue (TB) and safranin O (SO) staining demonstrated homogeneous glycosaminoglycan production throughout the KGN-MP incorporated MSC aggregates. The curcumin treatment efficiently reduced the expressions of hypertrophy markers by MSCs in vitro. The in vivo results showed that implantation of chondrogenic microtissues (KGN-MP incorporated MSC aggregates) using the curcumin loaded GelMA hydrogel resulted in cartilage tissue regeneration that had characteristic features close to the natural hyaline cartilage according to observational and histological results. Conclusions The use of this novel construct that contained chondrogenic cell blocks and curcumin is highly desired for cartilage regeneration. Graphical abstract

【 授权许可】

Unknown