Increased Chondrogenic Potential of Mesenchymal Cells From Adipose Tissue Versus Bone Marrow-Derived Cells in Osteoarthritic In Vitro Models

被引:31
|
作者
Pagani, Stefania [1 ]
Borsari, Veronica [2 ]
Veronesi, Francesca [1 ]
Ferrari, Andrea [1 ]
Cepollaro, Simona [1 ,3 ]
Torricelli, Paola [1 ]
Filardo, Giuseppe [4 ]
Fini, Milena [1 ]
机构
[1] Rizzoli Orthopaed Inst, Lab Preclin & Surg Studies, Via Barbiano 1-10, I-40136 Bologna, Italy
[2] Rizzoli Orthopaed Inst, Dept RIT Rizzoli, Lab Biocompatibil Technol Innovat & Adv Therapies, Bologna, Italy
[3] Univ Bologna, Dept Med & Surg Sci, Bologna, Italy
[4] Univ Bologna, Rizzoli Orthopaed Inst, Biomech Lab Clin 2, Bologna, Italy
关键词
NECROSIS-FACTOR-ALPHA; SYNOVIAL-FLUID; STEM-CELLS; CARTILAGE REGENERATION; RHEUMATOID-ARTHRITIS; KNEE OSTEOARTHRITIS; CHONDROCYTES; DEGENERATION; DIFFERENTIATION; INFLAMMATION;
D O I
10.1002/jcp.25651
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Primarily, to compare the behavior of human mesenchymal stem cells (MSCs) derived from bone marrow (hBMSCs) and adipose tissue (hADSCs) in an osteoarthritic (OA) microenvironment; secondly, to investigate the reaction of these cell types in two alternative in vitro culture systems, obtained by using TNF alpha and/or IL1 beta as inflammation mediators, or by using synovial fluid harvested by OA patients (OSF) to simulate the complex inflamed knee microenvironment. 3D micromass cultures of hBMSCs or hADSCs were grown in chondrogenic medium (CTR), in the presence of TNF alpha and/or IL1 beta, or synovial fluid from OA patients. After 1 month of culture, the chondrogenic differentiation of micromasses was evaluated by gene expression, matrix composition, and organization. Both hMSCs types formed mature micromasses in CTR, but a better response of hADSCs to the inflammatory environment was documented by micromass area and Bern score evaluations. The addition of OSF elicited a milder reaction than with TNF alpha and/or IL1 beta by both cell types, probably due to the presence of both catabolic and protective factors. In particular, SOX9 and ACAN gene expression and GAG synthesis were more abundant in hADSCs than hBMSCs when cultured in OSF. The expression of MMP1 was increased for both hMSCs in inflammatory conditions, but in particular by hBMSCs. hADSCs showed an increased chondrogenic potential in inflammatory culture systems, suggesting a better response of hADSCs in theOAenvironment, thus underlining the importance of appropriate in vitro models to study MSCs and potential advantages of using these cells for future clinical applications. (C) 2016 Wiley Periodicals, Inc.
引用
收藏
页码:1478 / 1488
页数:11
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