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A Change of Heart: Human Cardiac Tissue Engineering as a Platform for Drug Development

PURPOSE OF REVIEW: Human cardiac tissue engineering holds great promise for early detection of drug-related cardiac toxicity and arrhythmogenicity during drug discovery and development. We describe shortcomings of the current drug development pathway, recent advances in the development of cardiac ti...

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Autores principales: Bremner, Samantha B., Gaffney, Karen S., Sniadecki, Nathan J., Mack, David L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897733/
https://www.ncbi.nlm.nih.gov/pubmed/35247166
http://dx.doi.org/10.1007/s11886-022-01668-7
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author Bremner, Samantha B.
Gaffney, Karen S.
Sniadecki, Nathan J.
Mack, David L.
author_facet Bremner, Samantha B.
Gaffney, Karen S.
Sniadecki, Nathan J.
Mack, David L.
author_sort Bremner, Samantha B.
collection PubMed
description PURPOSE OF REVIEW: Human cardiac tissue engineering holds great promise for early detection of drug-related cardiac toxicity and arrhythmogenicity during drug discovery and development. We describe shortcomings of the current drug development pathway, recent advances in the development of cardiac tissue constructs as drug testing platforms, and the challenges remaining in their widespread adoption. RECENT FINDINGS: Human pluripotent stem cell-derived cardiomyocytes (hPSC-CMs) have been used to develop a variety of constructs including cardiac spheroids, microtissues, strips, rings, and chambers. Several ambitious studies have used these constructs to test a significant number of drugs, and while most have shown proper negative inotropic and arrhythmogenic responses, few have been able to demonstrate positive inotropy, indicative of relative hPSC-CM immaturity. SUMMARY: Several engineered human cardiac tissue platforms have demonstrated native cardiac physiology and proper drug responses. Future studies addressing hPSC-CM immaturity and inclusion of patient-specific cell lines will further advance the utility of such models for in vitro drug development.
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spelling pubmed-88977332022-03-07 A Change of Heart: Human Cardiac Tissue Engineering as a Platform for Drug Development Bremner, Samantha B. Gaffney, Karen S. Sniadecki, Nathan J. Mack, David L. Curr Cardiol Rep Regenerative Medicine (SM Wu, Section Editor) PURPOSE OF REVIEW: Human cardiac tissue engineering holds great promise for early detection of drug-related cardiac toxicity and arrhythmogenicity during drug discovery and development. We describe shortcomings of the current drug development pathway, recent advances in the development of cardiac tissue constructs as drug testing platforms, and the challenges remaining in their widespread adoption. RECENT FINDINGS: Human pluripotent stem cell-derived cardiomyocytes (hPSC-CMs) have been used to develop a variety of constructs including cardiac spheroids, microtissues, strips, rings, and chambers. Several ambitious studies have used these constructs to test a significant number of drugs, and while most have shown proper negative inotropic and arrhythmogenic responses, few have been able to demonstrate positive inotropy, indicative of relative hPSC-CM immaturity. SUMMARY: Several engineered human cardiac tissue platforms have demonstrated native cardiac physiology and proper drug responses. Future studies addressing hPSC-CM immaturity and inclusion of patient-specific cell lines will further advance the utility of such models for in vitro drug development. Springer US 2022-03-05 2022 /pmc/articles/PMC8897733/ /pubmed/35247166 http://dx.doi.org/10.1007/s11886-022-01668-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Regenerative Medicine (SM Wu, Section Editor)
Bremner, Samantha B.
Gaffney, Karen S.
Sniadecki, Nathan J.
Mack, David L.
A Change of Heart: Human Cardiac Tissue Engineering as a Platform for Drug Development
title A Change of Heart: Human Cardiac Tissue Engineering as a Platform for Drug Development
title_full A Change of Heart: Human Cardiac Tissue Engineering as a Platform for Drug Development
title_fullStr A Change of Heart: Human Cardiac Tissue Engineering as a Platform for Drug Development
title_full_unstemmed A Change of Heart: Human Cardiac Tissue Engineering as a Platform for Drug Development
title_short A Change of Heart: Human Cardiac Tissue Engineering as a Platform for Drug Development
title_sort change of heart: human cardiac tissue engineering as a platform for drug development
topic Regenerative Medicine (SM Wu, Section Editor)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897733/
https://www.ncbi.nlm.nih.gov/pubmed/35247166
http://dx.doi.org/10.1007/s11886-022-01668-7
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