Chamber-Specific Protein Expression during Direct Cardiac Reprogramming
Forced expression of core cardiogenic transcription factors can directly reprogram fibroblasts to induced cardiomyocyte-like cells (iCMs) in vitro and in vivo. This cardiac reprogramming approach provides a proof of concept for induced heart regeneration by converting a fibroblast fate to a cardiomy...
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doaj-d39beaf7a8c94116b609c45c25a239972021-07-01T00:17:25ZengMDPI AGCells2073-44092021-06-01101513151310.3390/cells10061513Chamber-Specific Protein Expression during Direct Cardiac ReprogrammingZhentao Zhang0Jesse Villalpando1Wenhui Zhang2Young-Jae Nam3Department of Medicine, Division of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, TN 37232, USADepartment of Medicine, Division of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, TN 37232, USADepartment of Medicine, Division of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, TN 37232, USADepartment of Medicine, Division of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, TN 37232, USAForced expression of core cardiogenic transcription factors can directly reprogram fibroblasts to induced cardiomyocyte-like cells (iCMs) in vitro and in vivo. This cardiac reprogramming approach provides a proof of concept for induced heart regeneration by converting a fibroblast fate to a cardiomyocyte fate. However, it remains elusive whether chamber-specific cardiomyocytes can be generated by cardiac reprogramming. Therefore, we assessed the ability of the cardiac reprogramming approach for chamber specification in vitro and in vivo. We found that in vivo cardiac reprogramming post-myocardial infarction exclusively induces a ventricular-like phenotype, while a major fraction of iCMs generated in vitro failed to determine their chamber identities. Our results suggest that in vivo cardiac reprogramming may have an inherent advantage of generating chamber-matched new cardiomyocytes as a potential heart regenerative approach.https://www.mdpi.com/2073-4409/10/6/1513reprogrammingfibroblastcardiomyocytechamber |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Zhentao Zhang Jesse Villalpando Wenhui Zhang Young-Jae Nam |
spellingShingle |
Zhentao Zhang Jesse Villalpando Wenhui Zhang Young-Jae Nam Chamber-Specific Protein Expression during Direct Cardiac Reprogramming Cells reprogramming fibroblast cardiomyocyte chamber |
author_facet |
Zhentao Zhang Jesse Villalpando Wenhui Zhang Young-Jae Nam |
author_sort |
Zhentao Zhang |
title |
Chamber-Specific Protein Expression during Direct Cardiac Reprogramming |
title_short |
Chamber-Specific Protein Expression during Direct Cardiac Reprogramming |
title_full |
Chamber-Specific Protein Expression during Direct Cardiac Reprogramming |
title_fullStr |
Chamber-Specific Protein Expression during Direct Cardiac Reprogramming |
title_full_unstemmed |
Chamber-Specific Protein Expression during Direct Cardiac Reprogramming |
title_sort |
chamber-specific protein expression during direct cardiac reprogramming |
publisher |
MDPI AG |
series |
Cells |
issn |
2073-4409 |
publishDate |
2021-06-01 |
description |
Forced expression of core cardiogenic transcription factors can directly reprogram fibroblasts to induced cardiomyocyte-like cells (iCMs) in vitro and in vivo. This cardiac reprogramming approach provides a proof of concept for induced heart regeneration by converting a fibroblast fate to a cardiomyocyte fate. However, it remains elusive whether chamber-specific cardiomyocytes can be generated by cardiac reprogramming. Therefore, we assessed the ability of the cardiac reprogramming approach for chamber specification in vitro and in vivo. We found that in vivo cardiac reprogramming post-myocardial infarction exclusively induces a ventricular-like phenotype, while a major fraction of iCMs generated in vitro failed to determine their chamber identities. Our results suggest that in vivo cardiac reprogramming may have an inherent advantage of generating chamber-matched new cardiomyocytes as a potential heart regenerative approach. |
topic |
reprogramming fibroblast cardiomyocyte chamber |
url |
https://www.mdpi.com/2073-4409/10/6/1513 |
work_keys_str_mv |
AT zhentaozhang chamberspecificproteinexpressionduringdirectcardiacreprogramming AT jessevillalpando chamberspecificproteinexpressionduringdirectcardiacreprogramming AT wenhuizhang chamberspecificproteinexpressionduringdirectcardiacreprogramming AT youngjaenam chamberspecificproteinexpressionduringdirectcardiacreprogramming |
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1721349025010024448 |