Journal
JOURNAL OF NANOBIOTECHNOLOGY
Volume 20, Issue 1, Pages -Publisher
BMC
DOI: 10.1186/s12951-021-01230-7
Keywords
Decellularized extracellular matrix; Peptide; Recruitment; Chondrogenesis; Cartilage regeneration
Funding
- National Key R&D Program of China [2019YFA0110600]
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The regeneration and repair of articular cartilage is challenging due to its poor intrinsic healing ability. In this study, a combination of bone marrow stem cells and a modified chondrocyte extracellular matrix were used to create a scaffold that successfully recruited endogenous stem cells and promoted cartilage repair in rabbits.
Background: The regeneration and repair of articular cartilage remains a major challenge for clinicians and scientists due to the poor intrinsic healing of this tissue. Since cartilage injuries are often clinically irregular, tissue-engineered scaffolds that can be easily molded to fill cartilage defects of any shape that fit tightly into the host cartilage are needed. Method: In this study, bone marrow mesenchymal stem cell (BMSC) affinity peptide sequence PFSSTKT (PFS)-modified chondrocyte extracellular matrix (ECM) particles combined with GeIMA hydrogel were constructed. Results: In vitro experiments showed that the pore size and porosity of the solid-supported composite scaffolds were appropriate and that the scaffolds provided a three-dimensional microenvironment supporting cell adhesion, proliferation and chondrogenic differentiation. In vitro experiments also showed that GeIMA/ECM-PFS could regulate the migration of rabbit BMSCs. Two weeks after implantation in vivo, the GeIMA/ECM-PFS functional scaffold system promoted the recruitment of endogenous mesenchymal stem cells from the defect site. GeIMA/ECM-PFS achieved successful hyaline cartilage repair in rabbits in vivo, while the control treatment mostly resulted in fibrous tissue repair. Conclusion: This combination of endogenous cell recruitment and chondrogenesis is an ideal strategy for repairing irregular cartilage defects.
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