Reorganization of Metabolism during Cardiomyogenesis Implies Time-Specific Signaling Pathway Regulation

Understanding the cell differentiation process involves the characterization of signaling and regulatory pathways. The coordinated action involved in multilevel regulation determines the commitment of stem cells and their differentiation into a specific cell lineage. Cellular metabolism plays a rele...

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Main Authors: María Julia Barisón, Isabela Tiemy Pereira, Anny Waloski Robert, Bruno Dallagiovanna
Format: Article
Language:English
Published: MDPI AG 2021-01-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/22/3/1330
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author María Julia Barisón
Isabela Tiemy Pereira
Anny Waloski Robert
Bruno Dallagiovanna
author_facet María Julia Barisón
Isabela Tiemy Pereira
Anny Waloski Robert
Bruno Dallagiovanna
author_sort María Julia Barisón
collection DOAJ
description Understanding the cell differentiation process involves the characterization of signaling and regulatory pathways. The coordinated action involved in multilevel regulation determines the commitment of stem cells and their differentiation into a specific cell lineage. Cellular metabolism plays a relevant role in modulating the expression of genes, which act as sensors of the extra-and intracellular environment. In this work, we analyzed mRNAs associated with polysomes by focusing on the expression profile of metabolism-related genes during the cardiac differentiation of human embryonic stem cells (hESCs). We compared different time points during cardiac differentiation (pluripotency, embryoid body aggregation, cardiac mesoderm, cardiac progenitor and cardiomyocyte) and showed the immature cell profile of energy metabolism. Highly regulated canonical pathways are thoroughly discussed, such as those involved in metabolic signaling and lipid homeostasis. We reveal the critical relevance of retinoic X receptor (RXR) heterodimers in upstream retinoic acid metabolism and their relationship with thyroid hormone signaling. Additionally, we highlight the importance of lipid homeostasis and extracellular matrix component biosynthesis during cardiomyogenesis, providing new insights into how hESCs reorganize their metabolism during in vitro cardiac differentiation.
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spelling doaj.art-4d9aed3d3ab348d5ae86ae190689c46f2023-12-03T15:09:53ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-01-01223133010.3390/ijms22031330Reorganization of Metabolism during Cardiomyogenesis Implies Time-Specific Signaling Pathway RegulationMaría Julia Barisón0Isabela Tiemy Pereira1Anny Waloski Robert2Bruno Dallagiovanna3Basic Stem Cell Biology Laboratory, Instituto Carlos Chagas-FIOCRUZ-PR, Rua Professor Algacyr Munhoz Mader, 3775, Curitiba, PR 81350-010, BrazilBasic Stem Cell Biology Laboratory, Instituto Carlos Chagas-FIOCRUZ-PR, Rua Professor Algacyr Munhoz Mader, 3775, Curitiba, PR 81350-010, BrazilBasic Stem Cell Biology Laboratory, Instituto Carlos Chagas-FIOCRUZ-PR, Rua Professor Algacyr Munhoz Mader, 3775, Curitiba, PR 81350-010, BrazilBasic Stem Cell Biology Laboratory, Instituto Carlos Chagas-FIOCRUZ-PR, Rua Professor Algacyr Munhoz Mader, 3775, Curitiba, PR 81350-010, BrazilUnderstanding the cell differentiation process involves the characterization of signaling and regulatory pathways. The coordinated action involved in multilevel regulation determines the commitment of stem cells and their differentiation into a specific cell lineage. Cellular metabolism plays a relevant role in modulating the expression of genes, which act as sensors of the extra-and intracellular environment. In this work, we analyzed mRNAs associated with polysomes by focusing on the expression profile of metabolism-related genes during the cardiac differentiation of human embryonic stem cells (hESCs). We compared different time points during cardiac differentiation (pluripotency, embryoid body aggregation, cardiac mesoderm, cardiac progenitor and cardiomyocyte) and showed the immature cell profile of energy metabolism. Highly regulated canonical pathways are thoroughly discussed, such as those involved in metabolic signaling and lipid homeostasis. We reveal the critical relevance of retinoic X receptor (RXR) heterodimers in upstream retinoic acid metabolism and their relationship with thyroid hormone signaling. Additionally, we highlight the importance of lipid homeostasis and extracellular matrix component biosynthesis during cardiomyogenesis, providing new insights into how hESCs reorganize their metabolism during in vitro cardiac differentiation.https://www.mdpi.com/1422-0067/22/3/1330hESCcardiomyocytescardiac differentiationmetabolismRXR heterodimersthyroid hormone
spellingShingle María Julia Barisón
Isabela Tiemy Pereira
Anny Waloski Robert
Bruno Dallagiovanna
Reorganization of Metabolism during Cardiomyogenesis Implies Time-Specific Signaling Pathway Regulation
International Journal of Molecular Sciences
hESC
cardiomyocytes
cardiac differentiation
metabolism
RXR heterodimers
thyroid hormone
title Reorganization of Metabolism during Cardiomyogenesis Implies Time-Specific Signaling Pathway Regulation
title_full Reorganization of Metabolism during Cardiomyogenesis Implies Time-Specific Signaling Pathway Regulation
title_fullStr Reorganization of Metabolism during Cardiomyogenesis Implies Time-Specific Signaling Pathway Regulation
title_full_unstemmed Reorganization of Metabolism during Cardiomyogenesis Implies Time-Specific Signaling Pathway Regulation
title_short Reorganization of Metabolism during Cardiomyogenesis Implies Time-Specific Signaling Pathway Regulation
title_sort reorganization of metabolism during cardiomyogenesis implies time specific signaling pathway regulation
topic hESC
cardiomyocytes
cardiac differentiation
metabolism
RXR heterodimers
thyroid hormone
url https://www.mdpi.com/1422-0067/22/3/1330
work_keys_str_mv AT mariajuliabarison reorganizationofmetabolismduringcardiomyogenesisimpliestimespecificsignalingpathwayregulation
AT isabelatiemypereira reorganizationofmetabolismduringcardiomyogenesisimpliestimespecificsignalingpathwayregulation
AT annywaloskirobert reorganizationofmetabolismduringcardiomyogenesisimpliestimespecificsignalingpathwayregulation
AT brunodallagiovanna reorganizationofmetabolismduringcardiomyogenesisimpliestimespecificsignalingpathwayregulation