Effect of Dynamic Culture and Periodic Compression on Human Mesenchymal Stem Cell Proliferation and Chondrogenesis

被引:67
作者
Guo, Ting [1 ]
Yu, Li [2 ]
Lim, Casey G. [1 ]
Goodley, Addison S. [1 ]
Xiao, Xuan [3 ]
Placone, Jesse K. [1 ]
Ferlin, Kimberly M. [1 ]
Nguyen, Bao-Ngoc B. [1 ]
Hsieh, Adam H. [1 ]
Fisher, John P. [1 ]
机构
[1] Univ Maryland, Fischell Dept Bioengn, 3238 Jeong H Kim Engn Bldg, College Pk, MD 20742 USA
[2] Wuhan Univ, Zhongnan Hosp, Dept Orthoped, Wuhan 430072, Peoples R China
[3] Wuhan Univ, Renming Hosp, Dept Ophthalmol, Wuhan 430072, Peoples R China
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Mesenchymal stem cell; Chondrogenesis; Differentiation; Compression; Cartilage; Dynamic culture; TUBULAR PERFUSION SYSTEM; ARTICULAR-CARTILAGE; MATRIX PRODUCTION; PROGENITOR CELLS; EXPRESSION; CHONDROCYTES; BIOREACTOR; EXPANSION; PRESSURE; INTERFERES;
D O I
10.1007/s10439-015-1510-5
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
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.
引用
收藏
页码:2103 / 2113
页数:11
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