去细胞化
间充质干细胞
细胞外基质
球体
软骨发生
间质细胞
细胞生物学
化学
基质(化学分析)
生物医学工程
细胞
医学
生物
病理
体外
生物化学
色谱法
作者
David H. Ramos‐Rodriguez,Shierly W. Fok,Connor J. Dorais,Andrea C. Filler,Micaela Caserta,J. Kent Leach
出处
期刊:Tissue Engineering Part A
[Mary Ann Liebert, Inc.]
日期:2024-11-18
被引量:1
标识
DOI:10.1089/ten.tea.2024.0267
摘要
Cartilage regeneration is hindered due to the low proliferative capacity of chondrocytes and the avascular nature of cartilaginous tissue. Mesenchymal stromal cells (MSCs) are widely studied for cartilage tissue engineering, and the aggregation of MSCs into high-density cell spheroids facilitates chondrogenic differentiation due to increased cell-cell contact. Despite the promise of MSCs, the field would benefit from improved strategies to regulate the chondrogenic potential of MSCs differentiated from induced pluripotent stem cells (iPSCs), which are advantageous for their capacity to yield large numbers of required cells. We previously demonstrated the ability of MSC-secreted extracellular matrix (ECM) to promote MSC chondrogenic differentiation, but the combinatorial effect of iPSC-derived MSC (iMSC) spheroids, iMSC-derived decellularized ECM (idECM), and other stimuli (e.g., oxygen tension and transforming growth factor [TGF]-β) on chondrogenic potential has not been described. Similar to MSCs, iMSCs secreted a collagen-rich ECM. When incorporated into spheroids, idECM increased spheroid diameter and promoted chondrogenic differentiation. The combination of idECM loading, chondrogenic media, and hypoxia enhanced glycosaminoglycan (GAG) content 1.6-fold (40.9 ± 4.6 ng vs. 25.6 ± 3.3 ng,
科研通智能强力驱动
Strongly Powered by AbleSci AI