TY - JOUR
T1 - Cartilage-Derived Progenitor Cell-Laden Injectable Hydrogel-An Approach for Cartilage Tissue Regeneration
AU - Li, Xiaolin
AU - Sigen, A.
AU - Xu, Qian
AU - Alshehri, Fatma
AU - Zeng, Ming
AU - Zhou, Dezhong
AU - Li, Jun
AU - Zhou, Guangqian
AU - Wang, Wenxin
N1 - Publisher Copyright:
© 2020 American Chemical Society.
PY - 2020/8/17
Y1 - 2020/8/17
N2 - 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.
AB - 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.
KW - cartilage progenitor cells
KW - cartilage regeneration
KW - hyaluronic acid
KW - hyperbranched PEG macromer
KW - injectable hydrogel
UR - https://www.scopus.com/pages/publications/85090973574
U2 - 10.1021/acsabm.0c00294
DO - 10.1021/acsabm.0c00294
M3 - 文章
AN - SCOPUS:85090973574
SN - 2576-6422
VL - 3
SP - 4756
EP - 4765
JO - ACS Applied Bio Materials
JF - ACS Applied Bio Materials
IS - 8
ER -