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Epicardial SMARCA4 deletion exacerbates cardiac injury in myocardial infarction and is related to the inhibition of epicardial epithelial-mesenchymal transition.

Authors :
Ma, Xingyu
Zhao, Jianjun
Feng, Yi
Source :
Journal of Molecular & Cellular Cardiology. Jun2024, Vol. 191, p76-87. 12p.
Publication Year :
2024

Abstract

The reactivated adult epicardium produces epicardium-derived cells (EPDCs) via epithelial-mesenchymal transition (EMT) to benefit the recovery of the heart after myocardial infarction (MI). SMARCA4 is the core catalytic subunit of the chromatin re-modeling complex, which has the potential to target some reactivated epicardial genes in MI. However, the effects of epicardial SMARCA4 on MI remain uncertain. This study found that SMARCA4 was activated over time in epicardial cells following MI, and some of activated cells belonged to downstream differentiation types of EPDCs. This study used tamoxifen to induce lineage tracing and SMARCA4 deletion from epicardial cells in Wt1-CreER;Smarca4 fl/fl ;Rosa26-RFP adult mice. Epicardial SMARCA4 deletion reduces the number of epicardial cells in adult mice, which was related to changes in the activation, proliferation, and apoptosis of epicardial cells. Epicardial SMARCA4 deletion reduced collagen deposition and angiogenesis in the infarcted area, exacerbated cardiac injury in MI. The exacerbation of cardiac injury was related to the inhibition of generation and differentiation of EPDCs. The alterations in EPDCs were associated with inhibited transition between E -CAD and N-CAD during the epicardial EMT, coupled with the down-regulation of WT1, SNAIL1, and PDGF signaling. In conclusion, this study suggests that Epicardial SMARCA4 plays a critical role in cardiac injury caused by MI, and its regulatory mechanism is related to epicardial EMT. Epicardial SMARCA4 holds potential as a novel molecular target for treating MI. [Display omitted] • Lineage tracing and SMARCA4 deletion in epicardial cells were achieved using Wt1-CreER;Smarca4fl/fl;Rosa26-RFP mice. • Epicardial SMARCA4 deletion exacerbated cardiac injury in myocardial infarction. • Epicardial SMARCA4 deletion inhibited the generation and differentiation of EPDCs in myocardial infarction. • The effects of Epicardial SMARCA4 deletion on EPDCs were related to the obstruction of epicardial EMT. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00222828
Volume :
191
Database :
Academic Search Index
Journal :
Journal of Molecular & Cellular Cardiology
Publication Type :
Academic Journal
Accession number :
177375350
Full Text :
https://doi.org/10.1016/j.yjmcc.2024.05.001