Decellularized extracellular matrix bioinks and the external stimuli to enhance cardiac tissue development in vitro

被引:114
作者
Das, Sanskrita [1 ]
Kim, Seok-Won [2 ]
Choi, Yeong-Jin [2 ,3 ]
Lee, Sooyeon [1 ]
Lee, Se-Hwan [1 ]
Kong, Jeong-Sik [4 ]
Park, Hun-Jun [5 ]
Cho, Dong-Woo [2 ]
Jang, Jinah [1 ,2 ,4 ]
机构
[1] Pohang Univ Sci & Technol POSTECH, Dept Creat IT Engn, 77 Cheongam Ro, Pohang 37673, Kyungbuk, South Korea
[2] Pohang Univ Sci & Technol POSTECH, Dept Mech Engn, 77 Cheongam Ro, Pohang 37673, Kyungbuk, South Korea
[3] KIMS, Dept Adv Biomat Res, Mat Proc Innovat Res Div, 797 Changwon Daero, Changwon Si 51508, Gyeongsangnam D, South Korea
[4] Pohang Univ Sci & Technol POSTECH, Sch Interdisciplinary Biosci & Bioengn, 77 Cheongam Ro, Pohang 37673, Kyungbuk, South Korea
[5] Catholic Univ Korea, Div Cardiovasc Med, Coll Med, Cardiovasc Ctr,Seoul St Marys Hosp, 222 Banpodaero, Seoul 06591, South Korea
基金
新加坡国家研究基金会;
关键词
Engineered heart tissue; Decellularized extracellular matrix; 3D bioprinting; Bioink; External stimuli; STEM-CELLS; FUNCTIONAL IMPROVEMENT; ENGINEERED MYOCARDIUM; MECHANICAL-PROPERTIES; SUBSTRATE STIFFNESS; HEART; COLLAGEN; DIFFERENTIATION; PROLIFERATION; SARCOMERE;
D O I
10.1016/j.actbio.2019.04.026
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Engineered heart tissue (EHT) has ample potential as a model for in vitro tissue modeling or tissue regeneration. Using 3D cell printing technology, various hydrogels have been utilized as bioinks to fabricate EHT to date. However, its efficacy has remained limited due to poor functional properties of the cultured cardiomyocytes stemming from a lack of proper microenvironmental cues. Specifically, the surrounding matrix plays a key role in modulating cardiomyocyte differentiation and maturation. Recently, the use of heart tissue-derived extracellular matrix (hdECM) bioink has come to be seen as one of the most promising candidates due to its functional and structural similarities to native tissue. Here, we demonstrated a correlation between the synthesis of cardiomyocyte-specific proteins and the surrounding microenvironment irrespective of the similar material chemistry. Primary cardiomyocytes isolated from neonatal rats were encapsulated in different composition and concentration of bioinks (hdECM and collagen). The bioinks were sequentially printed using an extrusion-based 3D bioprinter and cultured either statically or dynamically. Qualitative and quantitative evaluation revealed enhanced maturation of cardiomyocytes in hdECM, unlike the collagen group under similar culture conditions. Specifically, 3D-printed EHT using a low concentration of hdECM promoted early differentiation of cardiomyocytes. Hence, the present study provides experimental insights regarding the establishment of a 3D-printed cardiac tissue model, highlighting that the matrix and the culture microenvironment can be decisive factors for cell-material interactions that affect cardiomyocyte maturation. Statement of Significance The regulation of signal transduction and responses to extracellular matrices (ECMs) is of particular relevance in tissue maturation. In particular, there is a clear need to understand the structural and phenotypical modulation in cardiomyocytes with respect to the surrounding microenvironment. Exploration of the key regulators, such as the compositional and the biophysical properties of bioinks associated directly with cell-cell and cell-matrix interactions would assist with the fabrication of cardiac tissue constructs with enhanced functionality. Hence, we documented the synergistic effects of surrounding matrices and culture conditions on the maturation of cardiomyocytes. Additionally, we highlighted the potential of using 3D bioprinting techniques to fabricate uniformly aligned cardiac constructs for mid- to high-throughput drug testing platforms that have great reproducibility and versatility. (C) 2019 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:188 / 200
页数:13
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