Mesenchymal stem cells loaded on 3D-printed gradient poly(ε-caprolactone)/methacrylated alginate composite scaffolds for cartilage tissue engineering

Author:

Cao Yanyan12,Cheng Peng3,Sang Shengbo1ORCID,Xiang Chuan3,An Yang4,Wei Xiaochun3,Shen Zhizhong1,Zhang Yixia5,Li Pengcui3

Affiliation:

1. Key Lab of Advanced Transducers and Intelligent Control System of the Ministry of Education, MicroNano System Research Center, College of Information and Computer, Taiyuan University of Technology, Taiyuan 030024, China

2. College of Information Science and Engineering, Hebei North University, Zhangjiakou 075000, China

3. Shanxi Key Laboratory of Bone and Soft Tissue Injury Repair, Department of Orthopedics, The Second Hospital of Shanxi Medical University, Taiyuan 030001, China

4. Department of Plastic Surgery, Peking University Third Hospital, Beijing 100191, China

5. Department of Biomedical Engineering, College of Biomedical Engineering, Taiyuan University of Technology, Taiyuan 030024, China

Abstract

Abstract Cartilage has limited self-repair ability due to its avascular, alymphatic and aneural features. The combination of three-dimensional (3D) printing and tissue engineering provides an up-and-coming approach to address this issue. Here, we designed and fabricated a tri-layered (superficial layer (SL), middle layer (ML) and deep layer (DL)) stratified scaffold, inspired by the architecture of collagen fibers in native cartilage tissue. The scaffold was composed of 3D printed depth-dependent gradient poly(ε-caprolactone) (PCL) impregnated with methacrylated alginate (ALMA), and its morphological analysis and mechanical properties were tested. To prove the feasibility of the composite scaffolds for cartilage regeneration, the viability, proliferation, collagen deposition and chondrogenic differentiation of embedded rat bone marrow mesenchymal stem cells (BMSCs) in the scaffolds were assessed by Live/dead assay, CCK-8, DNA content, cell morphology, immunofluorescence and real-time reverse transcription polymerase chain reaction. BMSCs-loaded gradient PCL/ALMA scaffolds showed excellent cell survival, cell proliferation, cell morphology, collagen II deposition and hopeful chondrogenic differentiation compared with three individual-layer scaffolds. Hence, our study demonstrates the potential use of the gradient PCL/ALMA construct for enhanced cartilage tissue engineering.

Funder

National Natural Science Foundation of China

National Key Research and Development Program

Shanxi Provincial Key Research and Development Project

Beijing Natural Science Foundation

Publisher

Oxford University Press (OUP)

Subject

Biomaterials

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