Multidimensional assembly using layer-by-layer deposition for synchronized cardiac macro tissues

被引:3
|
作者
Jang, Yongjun [1 ]
Jung, Da Jung [2 ]
Choi, Seung-Cheol [3 ]
Lim, Do-Sun [3 ]
Kim, Jong-Hoon [4 ]
Jeoung, Gi Seok [2 ]
Kim, Jongseong [1 ]
Park, Yongdoo [1 ]
机构
[1] Korea Univ, Coll Med, Dept Biomed Sci, Seoul, South Korea
[2] Asan Med Ctr, Biomed Engn Res Ctr, Asan Inst Life Sci, Seoul, South Korea
[3] Korea Univ, Cardiovasc Ctr, Dept Cardiol, Anam Hosp, Seoul, South Korea
[4] Korea Univ, Coll Life Sci & Biotechnol, Dept Biotechnol, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
CELL-DERIVED CARDIOMYOCYTES; EXTRACELLULAR-MATRIX; SELF-ORGANIZATION; STEM; MATURATION; FABRICATION; MYOCARDIUM; CONSTRUCTS; COCULTURE; SCAFFOLDS;
D O I
10.1039/d0ra01577f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The fabrication of biomimetic structures for tissues and organs is emerging in the fields of biomedical engineering and precision medicine. While current progress in biomedical research provides a number of biofabrication methods, the construction of multi-dimensional cardiac tissue is highly challenging due to difficulties in the maturation and synchronization of cardiomyocytes (CMs) in conjunction with other types of cells, such as myofibroblasts and endothelial cells. Here, we show a simple fabrication methodology to construct multi-dimensional cardiac macro tissue (mCMT) by layer-by-layer (LBL) deposition of cells on micro patterned PDMS. mCMTs formed by LBL deposition of pluripotent stem cell (PSC)-derived cardiomyocytes and cardiac fibroblasts formed 3D patterned structures with synchronized beating characteristics. We also demonstrate that cardiac maturation factors such as the gene expression of MLC2v and cTNI and formation of sarcomeres in mCMTs were significantly enhanced by LBL deposition and growth factors during the maturation process. Fabrication of matured mCMTs with synchronized beating enables providing an efficient platform for evaluating the efficacy and toxicity of drug candidates. These results have important implications because mCMTs are applicable to diverse in vitro studies and drug screening methods that require tissue-like structures and functions in a physiological environment.
引用
收藏
页码:18806 / 18815
页数:10
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