Glucosamine/collagen assembled biomimetic nanofibrous mats via LBL deposition for cartilage engineering

细胞外基质 化学 静电纺丝 材料科学 生物物理学 软骨 氨基葡萄糖 粘附 化学工程 基质(化学分析) 糖胺聚糖 纳米技术 生物医学工程 聚合物 生物化学 解剖 有机化学 色谱法 工程类 生物 医学
作者
Guomin Wu,Xiao Ma,Yiding Wang,Liancheng Fan,Yining Wang,Hongbing Deng
出处
期刊:Applied Surface Science [Elsevier]
卷期号:540: 148335-148335 被引量:2
标识
DOI:10.1016/j.apsusc.2020.148335
摘要

In order to highly simulate the chondrocyte extracellular matrix, electrospinning and layer-by-layer (LBL) self-assembly techniques were applied in this study. Polycaprolactone (PCL) with good mechanical property was selected as the substrate, while D-glucosamine sulfate (GAS) and collagen type I (COL) with chondroprotective properties were coated on the surfaces of PCL nanofibers. The morphology, chemical and physical investigations suggested the successful deposition of GAS/COL, improved mechanical properties and significantly ameliorated surfaces hydrophilicity after LBL medication. The release of GAS/COL was proved to be slow and sustainable. Besides, CCK-8 assay and cell morphology observation manifested that LBL structured mats were more suitable for rat articular chondrocytes (rACs) adhesion and proliferation, while quantitative Real-Time polymerase chain reaction analysis and glycosaminoglycans (GAG) production measurement indicated the introduction of GAS/COL upregulated glucuronosyltransferase I (GlcAT-I) gene expression and GAG content in rACs. Additionally, LBL structured mats induced GlcAT-I expression and reduced interleukin‐1β (IL‐1β) and Matrix metalloproteinases 13 (MMP13) expression in IL‐1β-induced rACs. Moreover, subcutaneous model in SCID mice further confirmed that GAS/COL modified PCL mat could facilitate the GAG production and collagen type II expression of rACs.
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