Near-Field Direct Write Microfiber-Reinforced Collagen Hydrogel Scaffolds for Articular Cartilage Regeneration

IF 0.8 Q4 MATERIALS SCIENCE, BIOMATERIALS Nano Life Pub Date : 2021-07-27 DOI:10.1142/s1793984421410026
Zining Wang, Xinliang Ye, Yingxian Lin, Zhishan Tan, Yuming Liu, Jie Li, J. Yin, Dejian Zhu, Mingze Ma, Xiang Wang, B. Lu, Li Wang, Chong Wang
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Abstract

The demand for treating degenerative osteoarthritis is dramatically growing during the past decade due to the increasing aging population. Compared to arthroscopic debridement and injection of lubricating hydrogels, implantation of a cartilage tissue engineering scaffold with a customized architecture and excellent stem cell delivery ability has been deemed as a superior alternative to regenerate defected cartilage tissues. However, relatively low mechanical strength of cell-laden hydrogel limits its potential in treating diseased/defected cartilage or tissues with an anisotropic structure. In this study, a composite cell-laden scaffold composed of three-dimensional (3D) fibrous patterns which was made through near-field electrospinning direct write (NEDW) and mesenchymal stem cell (MSC)-laden collagen I (COL I) hydrogel was fabricated. The hydrogel acted as a favorable microenvironment to load cells and growth factors to facilitate chondrogenic differentiation while the 3D fibrous patterns made of poly(caprolactone)-reinforced hydrogels and provided the composite scaffolds with a precisely designed micro-architecture. Compared to hydrogel scaffold alone, the fabricated composite scaffold had significantly higher mechanical properties. The composite scaffolds were biocompatible and can accelerate the chondrogenic differentiation of MSCs by up-regulating the expression of SOX9, collagen II (COL II) and aggrecan (ACAN), when transforming growth factor (TGF)-[Formula: see text]1 was loaded in COL I hydrogel. However, the morphology of differentiated cells was not identical to that of the natural chondrocytes, suggesting that the modulation of initial MSC morphology is needed to pursue the target phenotype after the chondrogenic differentiation.
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近场直写微纤维增强胶原水凝胶支架用于关节软骨再生
在过去的十年里,由于人口老龄化的加剧,对治疗退行性骨关节炎的需求急剧增长。与关节镜下清创术和注射润滑水凝胶相比,植入具有定制结构和卓越干细胞递送能力的软骨组织工程支架被认为是再生缺损软骨组织的优越选择。然而,载有细胞的水凝胶相对较低的机械强度限制了其治疗病变/缺损软骨或具有各向异性结构的组织的潜力。在本研究中,通过近场静电纺丝直接写入(NEDW)和间充质干细胞(MSC)负载的I型胶原(COL I)水凝胶制备了由三维(3D)纤维图案组成的复合细胞负载支架。水凝胶作为负载细胞和生长因子的有利微环境,促进软骨分化,而由聚己内酯制成的3D纤维图案增强了水凝胶,并为复合支架提供了精确设计的微观结构。与单独的水凝胶支架相比,所制备的复合支架具有显著更高的力学性能。当转化生长因子(TGF)-[公式:见正文]1负载在COL I水凝胶中时,复合支架具有生物相容性,可以通过上调SOX9、COL II和聚集蛋白聚糖(ACAN)的表达来加速MSCs的软骨分化。然而,分化细胞的形态与天然软骨细胞的形态不同,这表明需要调节初始MSC形态,以在软骨分化后追求目标表型。
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来源期刊
Nano Life
Nano Life MATERIALS SCIENCE, BIOMATERIALS-
CiteScore
0.70
自引率
12.50%
发文量
14
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