Enrichment of CD146 + Adipose-Derived Stem Cells in Combination with Articular Cartilage Extracellular Matrix Scaffold Promotes Cartilage Regeneration

• Published in: Theranostics 2019-01, Vol.9 (17), p.5105-5121
• Main Authors: Li, Xu, Guo, Weimin, Zha, Kangkang, Jing, Xiaoguang, Wang, Mingjie, Zhang, Yu, Hao, Chunxiang, Gao, Shuang, Chen, Mingxue, Yuan, Zhiguo, Wang, Zhenyong, Zhang, Xueliang, Shen, Shi, Li, Haojiang, Zhang, Bin, Xian, Hai, Zhang, Yuan, Sui, Xiang, Qin, Ling, Peng, Jiang, Liu, Shuyun, Lu, Shibi, Guo, Quanyi
• Format: Article
• Language: English
• Subjects: Adipose Tissue - cytology; Animals; Antibodies; Apoptosis; Arthritis; Bone marrow; Cartilage; Cartilage, Articular - metabolism; Cartilage, Articular - physiology; CD146 Antigen - genetics; CD146 Antigen - metabolism; Cells, Cultured; Extracellular matrix; Extracellular Matrix - chemistry; Extracellular Matrix - metabolism; Humans; Mesenchymal Stem Cell Transplantation - methods; Mesenchymal Stem Cells - cytology; Mesenchymal Stem Cells - metabolism; Proteins; Rabbits; Rats; Rats, Sprague-Dawley; Regeneration; Research Paper; Software; Stem cells; Tissue engineering; Tissue Engineering - methods; Tissue Scaffolds - chemistry; Umbilical cord
• ISSN: 1838-7640; 1838-7640
• DOI: 10.7150/thno.33904

Heterogeneity of mesenchymal stem cells (MSCs) influences the cell therapy outcome and the application in tissue engineering. Also, the application of subpopulations of MSCs in cartilage regeneration remains poorly characterized. CD146+ MSCs are identified as the natural ancestors of MSCs and the expression of CD146 are indicative of greater pluripotency and self-renewal potential. Here, we sorted a CD146 subpopulation from adipose-derived mesenchymal stem cells (ADSCs) for cartilage regeneration. : CD146 ADSCs were sorted using magnetic activated cell sorting (MACS). Cell surface markers, viability, apoptosis and proliferation were evaluated . The molecular signatures were analyzed by mRNA and protein expression profiling. By intra-articular injections of cells in a rat osteochondral defect model, we assessed the role of the specific subpopulation in cartilage microenvironment. Finally, CD146 ADSCs were combined with articular cartilage extracellular matrix (ACECM) scaffold for long term (3, 6 months) cartilage repair. : The enriched CD146 ADSCs showed a high expression of stem cell and pericyte markers, good viability, and immune characteristics to avoid allogeneic rejection. Gene and protein expression profiles revealed that the CD146 ADSCs had different cellular functions especially in regulation inflammation. In a rat model, CD146 ADSCs showed a better inflammation-modulating property in the early stage of intra-articular injections. Importantly, CD146 ADSCs exhibited good biocompatibility with the ACECM scaffold and the CD146 cell-scaffold composites produced less subcutaneous inflammation. The combination of CD146 ADSCs with ACECM scaffold can promote better cartilage regeneration in the long term. : Our data elucidated the function of the CD146 ADSC subpopulation, established their role in promoting cartilage repair, and highlighted the significance of cell subpopulations as a novel therapeutic for cartilage regeneration.