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

Author:

Wang Zining1,Ye Xinliang1,Lin Yingxian1,Tan Zhishan1,Liu Yuming1,Li Jie1,Yin Jiawen1,Zhu Dejian1,Ma Mingze2,Wang Xiang1,Lu Bingheng1,Wang Li1,Wang Chong1ORCID

Affiliation:

1. School of Mechanical Engineering, Dongguan University of Technology, No. 1 University Road Songshan, Lake Dongguan, Guangdong 523808, China

2. Department of Biomedical Engineering, Southern University of Science and Technology, Shenzhen, Guangdong 518055, China

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.

Funder

Collaborative Innovation Center for Water Treatment Technology and Materials

Natural Science Foundation of Guangdong Province, China

Natural Science Foundation of China

Foundation Research Project of Shenzhen, China

Department of Education of Guangdong Province, China

foundation and applied fund of guangdong province, china

Publisher

World Scientific Pub Co Pte Ltd

Subject

General Medicine

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