Fabrication of scaffold-free tubular cardiac constructs using a Bio-3D printer

被引:118
作者
Arai, Kenichi [1 ]
Murata, Daiki [1 ]
Verissimo, Ana Raquel [1 ]
Mukae, Yosuke [2 ]
Itoh, Manabu [2 ]
Nakamura, Anna [1 ]
Morita, Shigeki [2 ]
Nakayama, Koichi [1 ]
机构
[1] Saga Univ, Fac Med, Dept Regenerat Med & Biomed Engn, Saga, Japan
[2] Saga Univ, Fac Med, Dept Thorac & Cardiovasc Surg, Saga, Japan
基金
日本学术振兴会;
关键词
PLURIPOTENT STEM-CELLS; HEART-TRANSPLANTATION; TISSUE; STIMULATION; MUSCLE; MOUSE;
D O I
10.1371/journal.pone.0209162
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
A major challenge in cardiac tissue engineering is the host's immune response to artificial materials. To overcome this problem, we established a scaffold-free system for assembling cell constructs using an automated Bio-3D printer. This printer has previously been used to fabricate other three-dimensional (3D) constructs, including liver, blood vessels, and cartilage. In the present study, we tested the function in vivo of scaffold-free cardiac tubular construct fabricated using this system. Cardiomyocytes derived from induced pluripotent stem cells (iCells), endothelial cells, and fibroblasts were combined to make the spheroids. Subsequently, tubular cardiac constructs were fabricated by Bio-3D printer placing the spheroids on a needle array. Notably, the spheroid fusion and beat rate in the constructs were observed while still on the needle array. After removal from the needle array, electrical stimulation was used to test responsiveness of the constructs. An increased beat rate was observed during stimulation. Importantly, the constructs returned to their initial beat rate after stimulation was stopped. In addition, histological analysis shows cellular reorganization occurring in the cardiac constructs, which may mimic that observed during organ transplantation. Taken together, our results indicate that these engineered cardiac tubular constructs, which address both the limited supply of donor tissues as well as the immune-induced transplant rejection, has potential to be used for both clinical and drug testing applications. To our knowledge, this is the first time that cardiac tubular constructs have been produced using optimized Bio-3D printing technique and subsequently tested for their use as cardiac pumps.
引用
收藏
页数:17
相关论文
共 37 条
[1]
Development of vascularized iPSC derived 3D-cardiomyocyte tissues by filtration Layer-by-Layer technique and their application for pharmaceutical assays [J].
Amano, Yuto ;
Nishiguchi, Akihiro ;
Matsusaki, Michiya ;
Iseoka, Hiroko ;
Miyagawa, Shigeru ;
Sawa, Yoshiki ;
Seo, Manabu ;
Yamaguchi, Takashi ;
Akashi, Mitsuru .
ACTA BIOMATERIALIA, 2016, 33 :110-121
[2]
Beauchamp P, 2015, TISSUE ENG PART C-ME, V21, P852, DOI [10.1089/ten.tec.2014.0376, 10.1089/ten.TEC.2014.0376]
[3]
Cell therapy, 3D culture systems and tissue engineering for cardiac regeneration [J].
Emmert, Maximilian Y. ;
Hitchcock, Robert W. ;
Hoerstrup, Simon P. .
ADVANCED DRUG DELIVERY REVIEWS, 2014, 69 :254-269
[4]
Physiologic force-frequency response in engineered heart muscle by electromechanical stimulation [J].
Godier-Furnemont, Amandine F. G. ;
Tiburcy, Malte ;
Wagner, Eva ;
Dewenter, Matthias ;
Laemmle, Simon ;
El-Armouche, Ali ;
Lehnart, Stephan E. ;
Vunjak-Novakovic, Gordana ;
Zimmermann, Wolfram-Hubertus .
BIOMATERIALS, 2015, 60 :82-91
[5]
High-Content Assay Multiplexing for Toxicity Screening in Induced Pluripotent Stem Cell-Derived Cardiomyocytes and Hepatocytes [J].
Grimm, Fabian Alexander ;
Iwata, Yasuhiro ;
Sirenko, Oksana ;
Bittner, Michael ;
Rusyn, Ivan .
ASSAY AND DRUG DEVELOPMENT TECHNOLOGIES, 2015, 13 (09) :529-546
[6]
Scaffold-Free Tubular Tissues Created by a Bio-3D Printer Undergo Remodeling and Endothelialization when Implanted in Rat Aortae [J].
Itoh, Manabu ;
Nakayama, Koichi ;
Noguchi, Ryo ;
Kamohara, Keiji ;
Furukawa, Kojirou ;
Uchihashi, Kazuyoshi ;
Toda, Shuji ;
Oyama, Jun-ichi ;
Node, Koichi ;
Morita, Shigeki .
PLOS ONE, 2015, 10 (09)
[7]
Tissue engineering by self-assembly of cells printed into topologically defined structures [J].
Jakab, Karoly ;
Norotte, Cyrille ;
Damon, Brook ;
Marga, Francoise ;
Neagu, Adrian ;
Besch-Williford, Cynthia L. ;
Kachurin, Anatoly ;
Church, Kenneth H. ;
Park, Hyoungshin ;
Mironov, Vladimir ;
Markwald, Roger ;
Vunjak-Novakovic, Gordana ;
Forgacs, Gabor .
TISSUE ENGINEERING PART A, 2008, 14 (03) :413-421
[8]
Myocardial tissue engineering [J].
Jawad, Hedeer ;
Lyon, Alex R. ;
Harding, Sian E. ;
Ali, Nadire N. ;
Boccaccini, Aldo R. .
BRITISH MEDICAL BULLETIN, 2008, 87 (01) :31-47
[9]
Current status of the implantable LVAD [J].
Kadakia, Sagar ;
Moore, Ryan ;
Ambur, Vishnu ;
Toyoda, Yoshiya .
GENERAL THORACIC AND CARDIOVASCULAR SURGERY, 2016, 64 (09) :501-508
[10]
Stage-Specific Optimization of Activin/Nodal and BMP Signaling Promotes Cardiac Differentiation of Mouse and Human Pluripotent Stem Cell Lines [J].
Kattman, Steven J. ;
Witty, Alec D. ;
Gagliardi, Mark ;
Dubois, Nicole C. ;
Niapour, Maryam ;
Hotta, Akitsu ;
Ellis, James ;
Keller, Gordon .
CELL STEM CELL, 2011, 8 (02) :228-240