Bioinspired onion epithelium-like structure promotes the maturation of cardiomyocytes derived from human pluripotent stem cells

被引:34
|
作者
Xu, Cong [1 ,2 ]
Wang, Li [1 ,2 ]
Yu, Yue [1 ,2 ]
Yin, Fangchao [1 ,2 ]
Zhang, Xiaoqing [1 ]
Jiang, Lei [1 ,2 ]
Qin, Jianhua [1 ,2 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Dept Biotechnol, Dalian, Peoples R China
[2] Univ Chinese Acad Sci, Beijing, Peoples R China
基金
对外科技合作项目(国际科技项目);
关键词
FUNCTIONAL MATURATION; HUMAN MYOCARDIUM; CULTURE MODEL; BETA-CATENIN; HEART; GENERATION; CONTRACTILITY; GROWTH; CHIP; CUES;
D O I
10.1039/c7bm00132k
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Organized cardiomyocyte alignment is critical to maintain the mechanical properties of the heart. In this study, we present a new and simple strategy to fabricate a biomimetic microchip designed with an onion epithelium-like structure and investigate the guided behavior of human induced pluripotent stem cell derived cardiomyocytes (hiPSC-CMs) on the substrate. The hiPSC-CMs were observed to be confined by the three dimensional surficial features morphologically, analogous to the in vivo microenvironment, and exhibited an organized anisotropic alignment on the onion epithelium-like structure with good beating function. The calcium imaging of hiPSC-CMs demonstrated a more mature Ca2+ spark pattern as well. Furthermore, the expression of sarcomere genes (TNNI3, MYH6 and MYH7), potassium channel genes (KCNE1 and KCNH2), and calcium channel genes (RYR2) was significantly up-regulated on the substrate with an onion epithelium-like structure instead of the surface without the structure, indicating a more matured status of cardiomyocytes induced by this structure. It appears that the biomimetic micro-patterned structure, analogous to in vivo cellular organization, is an important factor that might promote the maturation of hiPSC-CMs, providing new biological insights to guide hiPSC-CM maturation by biophysical factors. The established approach may offer an effective in vitro model for investigating cardiomyocyte differentiation, maturation and tissue engineering applications.
引用
收藏
页码:1810 / 1819
页数:10
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