A bioresponsive hydrogel tuned to chondrogenesis of human mesenchymal stem cells

被引:102
作者
Bahney, Chelsea S. [1 ,2 ]
Hsu, Chih-Wei [3 ]
Yoo, Jung U. [1 ]
West, Jennifer L. [3 ]
Johnstone, Brian [1 ,2 ]
机构
[1] Oregon Hlth & Sci Univ, Dept Orthopaed & Rehabil, Portland, OR 97239 USA
[2] Oregon Hlth & Sci Univ, Dept Cell & Dev Biol, Portland, OR 97239 USA
[3] Rice Univ, Dept Bioengn, Houston, TX USA
关键词
biodegradable scaffold; cartilage tissue engineering; matrix metalloproteinase; poly(ethylene glycol) diacrylate; matrilysin; HYALURONIC-ACID HYDROGELS; IN-VITRO CHONDROGENESIS; POLY(ETHYLENE GLYCOL); EXTRACELLULAR-MATRIX; ARTICULAR-CARTILAGE; CONTROLLED DIFFERENTIATION; TISSUE REGENERATION; AMINO PROPEPTIDE; DEGRADATION; MATRILYSIN;
D O I
10.1096/fj.10-165514
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cartilage tissue engineering aims to replace damaged or diseased tissue with a functional regenerate that restores joint function. Scaffolds are used to deliver cells and facilitate tissue development, but they can also interfere with the structural assembly of the cartilage matrix. Biodegradable scaffolds have been proposed as a means to improve matrix deposition and the biomechanical properties of neocartilage. The challenge is designing scaffolds with appropriate degradation rates, ideally such that scaffold degradation is proportional to matrix deposition. In this study, we developed a bioresponsive hydrogel with cell-mediated degradation aligned to the chondrogenic differentiation of human mesenchymal stem cells (hMSCs). We identified matrix metalloproteinase 7 (MMP7) as an enzyme with a temporal expression pattern that corresponded with cartilage development. By embedding MMP7 peptide substrates within a poly(ethylene glycol) diacrylate backbone, we built MMP7-sensitive hydrogels with distinct degradation rates. When MMP7-sensitive scaffolds were compared with nondegradable scaffolds in vitro, photoencapsulated hMSCs produced neocartilage constructs with more extensive collagenous matrices, as demonstrated through immunohistochemistry and biochemical quantification of matrix molecules. Furthermore, these changes translated into an increased dynamic compressive modulus. This work presents a practical strategy for designing biomaterials uniquely tuned to individual biological processes.-Bahney, C. S., Hsu, C.-W., Yoo, J. U., West, J. L., Johnstone, B. A bioresponsive hydrogel tuned to chondrogenesis of human mesenchymal stem cells. FASEB J. 25, 1486-1496 (2011). www.fasebj.org
引用
收藏
页码:1486 / 1496
页数:11
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