Thavandiran, N and Dubois, N and Mikryukov, A and Massé, S and Beca, B and Simmons, CA and Deshpande, VS and McGarry, JP and Chen, CS and Nanthakumar, K and Keller, GM and Radisic, M and Zandstra, PW (2013) Design and formulation of functional pluripotent stem cell-derived cardiac microtissues. Proc Natl Acad Sci U S A, 110. E4698-E4707.Full text not available from this repository.
Access to robust and information-rich human cardiac tissue models would accelerate drug-based strategies for treating heart disease. Despite significant effort, the generation of high-fidelity adult-like human cardiac tissue analogs remains challenging. We used computational modeling of tissue contraction and assembly mechanics in conjunction with microfabricated constraints to guide the design of aligned and functional 3D human pluripotent stem cell (hPSC)-derived cardiac microtissues that we term cardiac microwires (CMWs). Miniaturization of the platform circumvented the need for tissue vascularization and enabled higher-throughput image-based analysis of CMW drug responsiveness. CMW tissue properties could be tuned using electromechanical stimuli and cell composition. Specifically, controlling self-assembly of 3D tissues in aligned collagen, and pacing with point stimulation electrodes, were found to promote cardiac maturation-associated gene expression and in vivo-like electrical signal propagation. Furthermore, screening a range of hPSC-derived cardiac cell ratios identified that 75% NKX2 Homeobox 5 (NKX2-5)+ cardiomyocytes and 25% Cluster of Differentiation 90 OR (CD90)+ nonmyocytes optimized tissue remodeling dynamics and yielded enhanced structural and functional properties. Finally, we demonstrate the utility of the optimized platform in a tachycardic model of arrhythmogenesis, an aspect of cardiac electrophysiology not previously recapitulated in 3D in vitro hPSC-derived cardiac microtissue models. The design criteria identified with our CMW platform should accelerate the development of predictive in vitro assays of human heart tissue function.
|Uncontrolled Keywords:||arrhythmia disease model cardiac toxicity heart regeneration microfabrication tissue engineering Antigens, Thy-1 Biomechanical Phenomena Cellular Microenvironment Electric Stimulation Finite Element Analysis Homeodomain Proteins Humans Myocardium Pluripotent Stem Cells Tissue Engineering Transcription Factors|
|Divisions:||Div C > Materials Engineering|
|Depositing User:||Cron Job|
|Date Deposited:||07 Mar 2014 11:25|
|Last Modified:||11 Aug 2014 01:09|
Actions (login required)