Normandie University, UNICAEN, BIOTARGEN, 14000 Caen, France.
Center of Imaging and Research on Locomotor Affections in Equines, Ecole Vétérinaire d'Alfort, Université Paris-Est, 14430 Goustranville, France.
Int J Mol Sci. 2018 Feb 10;19(2):537. doi: 10.3390/ijms19020537.
Cartilage engineering is a new strategy for the treatment of cartilage damage due to osteoarthritis or trauma in humans. Racehorses are exposed to the same type of cartilage damage and the anatomical, cellular, and biochemical properties of their cartilage are comparable to those of human cartilage, making the horse an excellent model for the development of cartilage engineering. Human mesenchymal stem cells (MSCs) differentiated into chondrocytes with chondrogenic factors in a biomaterial appears to be a promising therapeutic approach for direct implantation and cartilage repair. Here, we characterized equine umbilical cord blood-derived MSCs (eUCB-MSCs) and evaluated their potential for chondrocyte differentiation for use in cartilage repair therapy. Our results show that isolated eUCB-MSCs had high proliferative capacity and differentiated easily into osteoblasts and chondrocytes, but not into adipocytes. A three-dimensional (3D) culture approach with the chondrogenic factors BMP-2 and TGF-β1 potentiated chondrogenic differentiation with a significant increase in cartilage-specific markers at the mRNA level (, , ) and the protein level (type II and IIB collagen) without an increase in hypertrophic chondrocyte markers ( and ) in normoxia and in hypoxia. However, these chondrogenic factors caused an increase in type I collagen, which can be reduced using small interfering RNA targeting . This study provides robust data on MSCs characterization and demonstrates that eUCB-MSCs have a great potential for cartilage tissue engineering.
软骨工程是一种治疗人类骨关节炎或创伤导致的软骨损伤的新策略。赛马也会受到同样类型的软骨损伤,其软骨的解剖学、细胞和生化特性与人软骨相似,这使得马成为软骨工程发展的优秀模型。在生物材料中,用软骨形成因子将人骨髓间充质干细胞 (MSCs) 分化为软骨细胞,似乎是一种很有前途的直接植入和软骨修复的治疗方法。在这里,我们对来自马脐带血的间充质干细胞 (eUCB-MSCs) 进行了特征描述,并评估了它们用于软骨修复治疗的软骨细胞分化潜力。我们的结果表明,分离的 eUCB-MSCs 具有高增殖能力,并且容易分化为成骨细胞和软骨细胞,但不会分化为脂肪细胞。在三维 (3D) 培养中加入软骨形成因子 BMP-2 和 TGF-β1,在常氧和低氧条件下,在 mRNA 水平(、和)和蛋白水平(II 型和 IIB 胶原)显著增加软骨特异性标志物的同时,促进软骨分化(),而不会增加肥大软骨细胞标志物(和)。然而,这些软骨形成因子会导致 I 型胶原增加,而使用针对的小干扰 RNA 可以减少 I 型胶原的增加。本研究提供了关于 MSC 特征描述的可靠数据,并证明 eUCB-MSCs 具有很大的软骨组织工程潜力。