| Literature DB >> 35021723 |
Xiaolin Li1, Sigen A1, Qian Xu1, Fatma Alshehri2, Ming Zeng3, Dezhong Zhou4, Jun Li5, Guangqian Zhou6, Wenxin Wang1.
Abstract
Cartilage-derived progenitor cells (CPCs) with the capability of self-renewal and multilineage differentiation have been identified as a suitable cell source for cartilage tissue regeneration. Despite decades of development in cell-delivery techniques, improved approaches are still required to maintain cell viability, provide a supportive environment, and implement appropriate cues to guide cartilage regeneration. This research work develops an injectable in situ gelation system as a cell carrier for CPCs to overcome cell-delivery drawbacks. The hydrogel was fabricated through a thiol-ene Michael addition reaction by cross-linking thiol-functionalized hyaluronic acid and hyperbranched poly(ethylene glycol) multi-acrylate macromer. The sol-gel transition, mechanical properties, microstructure, and degradation profile of the hydrogels were evaluated to ensure physical support, cell migration, and nutrient exchange within the system. Encapsulated CPCs maintained a high level of cell viability and proliferation property. Reverse transcription-quantitative real-time polymerase chain reaction confirmed that the extracellular matrix (ECM) secretion was enhanced under chondrogenic conditions. Moreover, the downregulated inflammation gene expression indicated the anti-inflammation ability of encapsulated CPCs. The study demonstrates that this rapid in situ forming hydrogel has excellent potential as a CPC delivery carrier by accelerating ECM production and retaining the phenotype and function of encapsulated CPCs.Entities:
Keywords: cartilage progenitor cells; cartilage regeneration; hyaluronic acid; hyperbranched PEG macromer; injectable hydrogel
Year: 2020 PMID: 35021723 DOI: 10.1021/acsabm.0c00294
Source DB: PubMed Journal: ACS Appl Bio Mater ISSN: 2576-6422