Investigating cellulose derived glycosaminoglycan mimetic scaffolds for cartilage tissue engineering applications

被引:30
作者
Huang, G. Portocarrero [1 ]
Molina, A. [1 ]
Tran, N. [1 ]
Collins, G. [1 ]
Arinzeh, Treena Livingston [1 ]
机构
[1] New Jersey Inst Technol, Dept Biomed Engn, 614 Fenster Hall, Newark, NJ 07102 USA
基金
美国国家科学基金会;
关键词
cellulose sulfate; biomimetic; mesenchymal stem cells; electrospinning; transforming growth factor-beta; chondrogenesis; MESENCHYMAL STEM-CELLS; GROWTH-FACTOR-BETA; CHONDROITIN SULFATE; CROSS-LINKING; CHONDROGENIC DIFFERENTIATION; ARTICULAR-CARTILAGE; BONE-MARROW; IN-VITRO; COLLAGEN; GELATIN;
D O I
10.1002/term.2331
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Articular cartilage has a limited capacity to heal and, currently, no treatment exists that can restore normal hyaline cartilage. Creating tissue engineering scaffolds that more closely mimic the native extracellular matrix may be an attractive approach. Glycosaminoglycans, which are present in native cartilage tissue, provide signalling and structural cues to cells. This study evaluated the use of a glycosaminoglycan mimetic, derived from cellulose, as a potential scaffold for cartilage repair applications. Fully sulfated sodium cellulose sulfate (NaCS) was initially evaluated in soluble form as an additive to cell culture media. Human mesenchymal stem cell (MSC) chondrogenesis in pellet culture was enhanced with 0.01% NaCS added to induction media as demonstrated by significantly higher gene expression for type II collagen and aggrecan. NaCS was combined with gelatine to form fibrous scaffolds using the electrospinning technique. Scaffolds were characterized for fibre morphology, overall hydrolytic stability, protein/growth factor interaction and for supporting MSC chondrogenesis in vitro. Scaffolds immersed in phosphate buffered saline for up to 56days had no changes in swelling and no dissolution of NaCS as compared to day 0. Increasing concentrations of the model protein lysozyme and transforming growth factor-3 were detected on scaffolds with increasing concentrations of NaCS (p<0.05). MSC chondrogenesis was enhanced on the scaffold with the lowest NaCS concentration as seen with the highest collagen type II production, collagen type II immunostaining, and expression of cartilage-specific genes. These studies demonstrate the feasibility of cellulose sulfate as a scaffolding material for cartilage tissue engineering. Copyright (C) 2016 John Wiley & Sons, Ltd.
引用
收藏
页码:E592 / E603
页数:12
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