3Bs Research Group-Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, Zona Industrial da Gandra, S. Claudio do Barco, 4806-909 Caldas das Taipas, Guimarães, Portugal.
J Tissue Eng Regen Med. 2011 Oct;5(9):722-32. doi: 10.1002/term.372. Epub 2010 Dec 29.
Native articular cartilage is subjected to synovial fluid flow during normal joint function. Thus, it is believed that the morphogenesis of articular cartilage may be positively regulated by the application of similar stimulation in vitro. In the present study, the effect of fluid flow over the chondrogenic differentiation of human bone marrow-derived mesenchymal stem cells (hBM-MSCs) was investigated. We intended to find out whether the shear stress caused by perfusion of the medium through the constructs was capable of augmenting the differentiation process. Human BMSCs were isolated from bone marrow aspirates and were characterized by flow cytometry. After expansion, hBM-MSCs were seeded statically onto fibre mesh scaffolds, consisting of a blend of 50:50 chitosan:poly(butylene terephthalate adipate) (CPBTA). Constructs were cultured in a flow-perfusion bioreactor for 28 days, using complete medium for chondrogenesis supplemented by TGFβ3. An enhanced ECM deposition and collagen type II production was observed in the bioreactor samples when compared to the static controls. Moreover, it was observed that hBM-MSCs, in static cultures, take longer to differentiate. ECM accumulation in these samples is lower than in the bioreactor sections, and there is a significant difference in the expression of collagen type I. We found that the flow-induced shear stress has a beneficial effect on the chondrogenic differentiation of hMSCs.
在正常关节功能中,关节软骨会受到滑液的冲刷。因此,人们认为关节软骨的形态发生可能会受到体外类似刺激的正向调节。在本研究中,研究了流体流动对骨髓间充质干细胞(hBM-MSCs)软骨分化的影响。我们旨在探讨通过构建体中培养基的灌注产生的切变力是否能够增强分化过程。从骨髓抽吸物中分离出人 BMSCs,并通过流式细胞术进行鉴定。扩增后,hBM-MSCs 以静态方式接种到纤维网支架上,该支架由壳聚糖:聚对苯二甲酸丁二醇酯(CPBTA)50:50 的混合物组成。构建体在流灌注生物反应器中培养 28 天,使用补充 TGFβ3 的完整软骨形成培养基。与静态对照相比,在生物反应器样品中观察到增强的细胞外基质沉积和胶原 II 型产生。此外,观察到在静态培养中,hBM-MSCs 需要更长的时间来分化。这些样本中的细胞外基质积累低于生物反应器部分,并且胶原 I 型的表达存在显著差异。我们发现,流动诱导的切变力对 hMSCs 的软骨分化有有益的影响。