Notch Inhibition Enhances Cardiac Reprogramming by Increasing MEF2C Transcriptional Activity

Conversion of fibroblasts into functional cardiomyocytes represents a potential means of restoring cardiac function after myocardial infarction, but so far this process remains inefficient and little is known about its molecular mechanisms. Here we show that DAPT, a classical Notch inhibitor, enhanc...

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Vydáno v:Stem cell reports Ročník 8; číslo 3; s. 548 - 560
Hlavní autoři: Abad, Maria, Hashimoto, Hisayuki, Zhou, Huanyu, Morales, Maria Gabriela, Chen, Beibei, Bassel-Duby, Rhonda, Olson, Eric N.
Médium: Journal Article
Jazyk:angličtina
Vydáno: United States Elsevier Inc 14.03.2017
Elsevier
Témata:
Animals
Calcium Signaling - drug effects
cardiomyocytes
Cell Differentiation
cell-fate conversion
Cellular Reprogramming - drug effects
Cellular Reprogramming - genetics
DAPT
Diamines - pharmacology
direct cellular reprogramming
Electrophysiological Phenomena - drug effects
Gene Expression Profiling
Gene Expression Regulation, Developmental
heart regeneration
MEF2 Transcription Factors - metabolism
Mice
Myocytes, Cardiac - cytology
Myocytes, Cardiac - drug effects
Myocytes, Cardiac - metabolism
Notch signaling
Proto-Oncogene Proteins c-akt - genetics
Proto-Oncogene Proteins c-akt - metabolism
Receptors, Notch - metabolism
regenerative medicine
Sarcomeres - drug effects
Sarcomeres - metabolism
Signal Transduction
Thiazoles - pharmacology
Transcriptional Activation
Transcriptome
transdifferentiation
cardiomyocytes
direct cellular reprogramming
heart regeneration
Notch signaling
regenerative medicine
transdifferentiation
cell-fate conversion
DAPT
ISSN:2213-6711, 2213-6711
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Shrnutí:Conversion of fibroblasts into functional cardiomyocytes represents a potential means of restoring cardiac function after myocardial infarction, but so far this process remains inefficient and little is known about its molecular mechanisms. Here we show that DAPT, a classical Notch inhibitor, enhances the conversion of mouse fibroblasts into induced cardiac-like myocytes by the transcription factors GATA4, HAND2, MEF2C, and TBX5. DAPT cooperates with AKT kinase to further augment this process, resulting in up to 70% conversion efficiency. Moreover, DAPT promotes the acquisition of specific cardiomyocyte features, substantially increasing calcium flux, sarcomere structure, and the number of spontaneously beating cells. Transcriptome analysis shows that DAPT induces genetic programs related to muscle development, differentiation, and excitation-contraction coupling. Mechanistically, DAPT increases binding of the transcription factor MEF2C to the promoter regions of cardiac structural genes. These findings provide mechanistic insights into the reprogramming process and may have important implications for cardiac regeneration therapies. [Display omitted] •Notch activation is a barrier for GHMT-induced cardiac cell reprogramming•Notch blockade by DAPT improves GHMT-induced cardiac reprogramming•DAPT increases sarcomere organization, calcium flux, and beating in GHMT reprogramming•DAPT enhances transcriptional activity of MEF2C in GHMT reprogramming In this article, Olson and colleagues show that Notch signaling activation is a critical barrier for cardiac cell reprogramming. Notch signaling blockade by DAPT, a γ-secretase inhibitor, enhances fibroblast conversion to cardiomyocytes by increasing calcium flux, sarcomere structure, and beating. Mechanistically, Notch inhibition enhances the transcriptional activity of the cardiogenic transcription factor MEF2C, thereby enhancing expression of cardiac genes.
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ISSN:2213-6711
2213-6711
DOI:10.1016/j.stemcr.2017.01.025