Engineered platform to generate 3D cardiac tissues for modeling genetic cardiomyopathies

Studies to gain mechanistic understanding of heart dysfunction based on animal and traditional cell culture models have significant limitations. Animal models are low throughput and fail to recapitulate many aspects of human cardiac biology, and 2D culture models utilizing human induced pluripotent...

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Main Author: Luu, Rebeccah
Other Authors: Chen, Christopher S.
Language:en_US
Published: 2018
Subjects:
Online Access:https://hdl.handle.net/2144/30731
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spelling ndltd-bu.edu-oai-open.bu.edu-2144-307312019-01-08T15:44:27Z Engineered platform to generate 3D cardiac tissues for modeling genetic cardiomyopathies Luu, Rebeccah Chen, Christopher S. Biomedical engineering Genetic cardiomyopathy Induced pluripotent stem cell derived cardiomyocytes Tissue engineering Studies to gain mechanistic understanding of heart dysfunction based on animal and traditional cell culture models have significant limitations. Animal models are low throughput and fail to recapitulate many aspects of human cardiac biology, and 2D culture models utilizing human induced pluripotent stem cell derived cardiomyocytes (iPSC-CMs) are higher throughput but fail to incorporate one or more in vivo parameters, such as 3D architecture, electrical pacing and mechanical constraint. High throughput 3D tissue platforms could better recapitulate the in vivo microenvironment of cardiac tissue. Previous work from our group demonstrated an approach to build 3D cardiac microtissues based on photolithography-based fabrication of a MEMS device, but design limitations prevented further iterations. In this work, we used a 3D printing approach to engineer iPSC-CM-derived cardiac microtissues with different form factors. Microtissues generated in this platform increased in lifespan compared to the first-generation platform by more than 100%. When modeling mutations associated with genetic cardiomyopathy, functional and structural differences were observed between tissues composed of wild-type and mutant iPSC-CMs. These findings suggest that this micro-device platform can be potentially used for both mechanistic and drug discovery studies. 2020-07-02T00:00:00Z 2018-08-09T18:41:13Z 2018 2018-07-03T01:04:49Z Thesis/Dissertation https://hdl.handle.net/2144/30731 en_US
collection NDLTD
language en_US
sources NDLTD
topic Biomedical engineering
Genetic cardiomyopathy
Induced pluripotent stem cell derived cardiomyocytes
Tissue engineering
spellingShingle Biomedical engineering
Genetic cardiomyopathy
Induced pluripotent stem cell derived cardiomyocytes
Tissue engineering
Luu, Rebeccah
Engineered platform to generate 3D cardiac tissues for modeling genetic cardiomyopathies
description Studies to gain mechanistic understanding of heart dysfunction based on animal and traditional cell culture models have significant limitations. Animal models are low throughput and fail to recapitulate many aspects of human cardiac biology, and 2D culture models utilizing human induced pluripotent stem cell derived cardiomyocytes (iPSC-CMs) are higher throughput but fail to incorporate one or more in vivo parameters, such as 3D architecture, electrical pacing and mechanical constraint. High throughput 3D tissue platforms could better recapitulate the in vivo microenvironment of cardiac tissue. Previous work from our group demonstrated an approach to build 3D cardiac microtissues based on photolithography-based fabrication of a MEMS device, but design limitations prevented further iterations. In this work, we used a 3D printing approach to engineer iPSC-CM-derived cardiac microtissues with different form factors. Microtissues generated in this platform increased in lifespan compared to the first-generation platform by more than 100%. When modeling mutations associated with genetic cardiomyopathy, functional and structural differences were observed between tissues composed of wild-type and mutant iPSC-CMs. These findings suggest that this micro-device platform can be potentially used for both mechanistic and drug discovery studies. === 2020-07-02T00:00:00Z
author2 Chen, Christopher S.
author_facet Chen, Christopher S.
Luu, Rebeccah
author Luu, Rebeccah
author_sort Luu, Rebeccah
title Engineered platform to generate 3D cardiac tissues for modeling genetic cardiomyopathies
title_short Engineered platform to generate 3D cardiac tissues for modeling genetic cardiomyopathies
title_full Engineered platform to generate 3D cardiac tissues for modeling genetic cardiomyopathies
title_fullStr Engineered platform to generate 3D cardiac tissues for modeling genetic cardiomyopathies
title_full_unstemmed Engineered platform to generate 3D cardiac tissues for modeling genetic cardiomyopathies
title_sort engineered platform to generate 3d cardiac tissues for modeling genetic cardiomyopathies
publishDate 2018
url https://hdl.handle.net/2144/30731
work_keys_str_mv AT luurebeccah engineeredplatformtogenerate3dcardiactissuesformodelinggeneticcardiomyopathies
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