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Characterization of cardiac metabolism in iPSC-derived cardiomyocytes: lessons from maturation and disease modeling

BACKGROUND: Induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) have emerged as a powerful tool for disease modeling, though their immature nature currently limits translation into clinical practice. Maturation strategies increasingly pay attention to cardiac metabolism because of its pi...

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Autores principales: Vučković, Sofija, Dinani, Rafeeh, Nollet, Edgar E., Kuster, Diederik W. D., Buikema, Jan Willem, Houtkooper, Riekelt H., Nabben, Miranda, van der Velden, Jolanda, Goversen, Birgit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9308297/
https://www.ncbi.nlm.nih.gov/pubmed/35870954
http://dx.doi.org/10.1186/s13287-022-03021-9
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author Vučković, Sofija
Dinani, Rafeeh
Nollet, Edgar E.
Kuster, Diederik W. D.
Buikema, Jan Willem
Houtkooper, Riekelt H.
Nabben, Miranda
van der Velden, Jolanda
Goversen, Birgit
author_facet Vučković, Sofija
Dinani, Rafeeh
Nollet, Edgar E.
Kuster, Diederik W. D.
Buikema, Jan Willem
Houtkooper, Riekelt H.
Nabben, Miranda
van der Velden, Jolanda
Goversen, Birgit
author_sort Vučković, Sofija
collection PubMed
description BACKGROUND: Induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) have emerged as a powerful tool for disease modeling, though their immature nature currently limits translation into clinical practice. Maturation strategies increasingly pay attention to cardiac metabolism because of its pivotal role in cardiomyocyte development and function. Moreover, aberrances in cardiac metabolism are central to the pathogenesis of cardiac disease. Thus, proper modeling of human cardiac disease warrants careful characterization of the metabolic properties of iPSC-CMs. METHODS: Here, we examined the effect of maturation protocols on healthy iPSC-CMs applied in 23 studies and compared fold changes in functional metabolic characteristics to assess the level of maturation. In addition, pathological metabolic remodeling was assessed in 13 iPSC-CM studies that focus on hypertrophic cardiomyopathy (HCM), which is characterized by abnormalities in metabolism. RESULTS: Matured iPSC-CMs were characterized by mitochondrial maturation, increased oxidative capacity and enhanced fatty acid use for energy production. HCM iPSC-CMs presented varying degrees of metabolic remodeling ranging from compensatory to energy depletion stages, likely due to the different types of mutations and clinical phenotypes modeled. HCM further displayed early onset hypertrophy, independent of the type of mutation or disease stage. CONCLUSIONS: Maturation strategies improve the metabolic characteristics of iPSC-CMs, but not to the level of the adult heart. Therefore, a combination of maturation strategies might prove to be more effective. Due to early onset hypertrophy, HCM iPSC-CMs may be less suitable to detect early disease modifiers in HCM and might prove more useful to examine the effects of gene editing and new drugs in advanced disease stages. With this review, we provide an overview of the assays used for characterization of cardiac metabolism in iPSC-CMs and advise on which metabolic assays to include in future maturation and disease modeling studies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-022-03021-9.
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spelling pubmed-93082972022-07-24 Characterization of cardiac metabolism in iPSC-derived cardiomyocytes: lessons from maturation and disease modeling Vučković, Sofija Dinani, Rafeeh Nollet, Edgar E. Kuster, Diederik W. D. Buikema, Jan Willem Houtkooper, Riekelt H. Nabben, Miranda van der Velden, Jolanda Goversen, Birgit Stem Cell Res Ther Review BACKGROUND: Induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) have emerged as a powerful tool for disease modeling, though their immature nature currently limits translation into clinical practice. Maturation strategies increasingly pay attention to cardiac metabolism because of its pivotal role in cardiomyocyte development and function. Moreover, aberrances in cardiac metabolism are central to the pathogenesis of cardiac disease. Thus, proper modeling of human cardiac disease warrants careful characterization of the metabolic properties of iPSC-CMs. METHODS: Here, we examined the effect of maturation protocols on healthy iPSC-CMs applied in 23 studies and compared fold changes in functional metabolic characteristics to assess the level of maturation. In addition, pathological metabolic remodeling was assessed in 13 iPSC-CM studies that focus on hypertrophic cardiomyopathy (HCM), which is characterized by abnormalities in metabolism. RESULTS: Matured iPSC-CMs were characterized by mitochondrial maturation, increased oxidative capacity and enhanced fatty acid use for energy production. HCM iPSC-CMs presented varying degrees of metabolic remodeling ranging from compensatory to energy depletion stages, likely due to the different types of mutations and clinical phenotypes modeled. HCM further displayed early onset hypertrophy, independent of the type of mutation or disease stage. CONCLUSIONS: Maturation strategies improve the metabolic characteristics of iPSC-CMs, but not to the level of the adult heart. Therefore, a combination of maturation strategies might prove to be more effective. Due to early onset hypertrophy, HCM iPSC-CMs may be less suitable to detect early disease modifiers in HCM and might prove more useful to examine the effects of gene editing and new drugs in advanced disease stages. With this review, we provide an overview of the assays used for characterization of cardiac metabolism in iPSC-CMs and advise on which metabolic assays to include in future maturation and disease modeling studies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-022-03021-9. BioMed Central 2022-07-23 /pmc/articles/PMC9308297/ /pubmed/35870954 http://dx.doi.org/10.1186/s13287-022-03021-9 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Vučković, Sofija
Dinani, Rafeeh
Nollet, Edgar E.
Kuster, Diederik W. D.
Buikema, Jan Willem
Houtkooper, Riekelt H.
Nabben, Miranda
van der Velden, Jolanda
Goversen, Birgit
Characterization of cardiac metabolism in iPSC-derived cardiomyocytes: lessons from maturation and disease modeling
title Characterization of cardiac metabolism in iPSC-derived cardiomyocytes: lessons from maturation and disease modeling
title_full Characterization of cardiac metabolism in iPSC-derived cardiomyocytes: lessons from maturation and disease modeling
title_fullStr Characterization of cardiac metabolism in iPSC-derived cardiomyocytes: lessons from maturation and disease modeling
title_full_unstemmed Characterization of cardiac metabolism in iPSC-derived cardiomyocytes: lessons from maturation and disease modeling
title_short Characterization of cardiac metabolism in iPSC-derived cardiomyocytes: lessons from maturation and disease modeling
title_sort characterization of cardiac metabolism in ipsc-derived cardiomyocytes: lessons from maturation and disease modeling
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9308297/
https://www.ncbi.nlm.nih.gov/pubmed/35870954
http://dx.doi.org/10.1186/s13287-022-03021-9
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