自愈水凝胶
软骨
软骨发生
化学
细胞外基质
弹性蛋白
去细胞化
组织工程
透明软骨
糖胺聚糖
II型胶原
体外
细胞生物学
体内
脚手架
软骨细胞
生物医学工程
生物物理学
解剖
生物化学
骨关节炎
病理
关节软骨
生物
高分子化学
医学
替代医学
生物技术
作者
Melissa K. McHale,Lori A. Setton,Ashutosh Chilkoti
出处
期刊:Tissue Engineering
[Mary Ann Liebert]
日期:2005-11-01
卷期号:11 (11-12): 1768-1779
被引量:282
标识
DOI:10.1089/ten.2005.11.1768
摘要
Genetically engineered elastin-like polypeptide (ELP) hydrogels offer unique promise as scaffolds for cartilage tissue engineering because of the potential to promote chondrogenesis and to control mechanical properties. In this study, we designed and synthesized ELPs capable of undergoing enzyme- initiated gelation via tissue transglutaminase, with the ultimate goal of creating an injectable, in situ cross-linking scaffold to promote functional cartilage repair. Addition of the enzyme promoted ELP gel formation and chondrocyte encapsulation in a biocompatible process, which resulted in cartilage matrix synthesis in vitro and the potential to contribute to cartilage mechanical function in vivo. A significant increase in the accumulation of sulfated glycosaminoglycans was observed, and histological sections revealed the accumulation of a cartilaginous matrix rich in type II collagen and lacking in type I collagen, indicative of hyaline cartilage formation. These results provide evidence of chondrocytic phenotype maintenance for cells in the ELP hydrogels in vitro. In addition, the dynamic shear moduli of ELP hydrogels seeded with chondrocytes increased from 0.28 to 1.7 kPa during a 4-week culture period. This increase in the mechanical integrity of cross-linked ELP hydrogels suggests restructuring of the ELP matrix by deposition of functional cartilage extracellular matrix components.
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