Guo Ting, Yu Li, Lim Casey G, Goodley Addison S, Xiao Xuan, Placone Jesse K, Ferlin Kimberly M, Nguyen Bao-Ngoc B, Hsieh Adam H, Fisher John P
Fischell Department of Bioengineering, University of Maryland, 3238 Jeong H. Kim Engineering Building, College Park, MD, 20742, USA.
Department of Orthopedics, Zhongnan Hospital of Wuhan University, Wuhan, China.
Ann Biomed Eng. 2016 Jul;44(7):2103-13. doi: 10.1007/s10439-015-1510-5. Epub 2015 Nov 17.
We have recently developed a bioreactor that can apply both shear and compressive forces to engineered tissues in dynamic culture. In our system, alginate hydrogel beads with encapsulated human mesenchymal stem cells (hMSCs) were cultured under different dynamic conditions while subjected to periodic, compressive force. A customized pressure sensor was developed to track the pressure fluctuations when shear forces and compressive forces were applied. Compared to static culture, dynamic culture can maintain a higher cell population throughout the study. With the application of only shear stress, qRT-PCR and immunohistochemistry revealed that hMSCs experienced less chondrogenic differentiation than the static group. The second study showed that chondrogenic differentiation was enhanced by additional mechanical compression. After 14 days, alcian blue staining showed more extracellular matrix formed in the compression group. The upregulation of the positive chondrogenic markers such as Sox 9, aggrecan, and type II collagen were demonstrated by qPCR. Our bioreactor provides a novel approach to apply mechanical forces to engineered cartilage. Results suggest that a combination of dynamic culture with proper mechanical stimulation may promote efficient progenitor cell expansion in vitro, thereby allowing the culture of clinically relevant articular chondrocytes for the treatment of articular cartilage defects.
我们最近开发了一种生物反应器,它可以在动态培养中对工程组织施加剪切力和压缩力。在我们的系统中,包裹有人间充质干细胞(hMSCs)的藻酸盐水凝胶珠在不同的动态条件下培养,同时承受周期性的压缩力。开发了一种定制的压力传感器来跟踪施加剪切力和压缩力时的压力波动。与静态培养相比,动态培养在整个研究过程中可以维持更高的细胞数量。仅施加剪切应力时,qRT-PCR和免疫组织化学显示hMSCs经历的软骨生成分化比静态组少。第二项研究表明,额外的机械压缩可增强软骨生成分化。14天后,阿尔新蓝染色显示压缩组形成了更多的细胞外基质。qPCR证实了软骨生成阳性标志物如Sox 9、聚集蛋白聚糖和II型胶原的上调。我们的生物反应器提供了一种对工程软骨施加机械力的新方法。结果表明,动态培养与适当的机械刺激相结合可能会促进体外祖细胞的有效扩增,从而能够培养出临床上相关的关节软骨细胞用于治疗关节软骨缺损。