Hemodynamic Forces Regulate Cardiac Regeneration-Responsive Enhancer Activity during Ventricle Regeneration

• Published in: International journal of molecular sciences Vol. 22; no. 8; p. 3945
• Main Authors: Geng, Fang, Ma, Jinmin, Li, Xueyu, Hu, Zhengyue, Zhang, Ruilin
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 11.04.2021; MDPI
• Subjects: Ablation; Animals; Binding sites; Cardiomyocytes; Gene expression; Heart; Heart Ventricles - metabolism; Hemodynamics; Myocardium - metabolism; Regeneration; Tissue engineering; Ventricular Function; Zebrafish; Zebrafish - genetics; Zebrafish - metabolism; regeneration-responsive enhancer; heart regeneration; Notch signaling; hemodynamics
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms22083945

Cardiac regenerative capacity varies widely among vertebrates. Zebrafish can robustly regenerate injured hearts and are excellent models to study the mechanisms of heart regeneration. Recent studies have shown that enhancers are able to respond to injury and regulate the regeneration process. However, the mechanisms to activate these regeneration-responsive enhancers (RREs) remain poorly understood. Here, we utilized transient and transgenic analysis combined with a larval zebrafish ventricle ablation model to explore the activation and regulation of a representative RRE. lepb-linked enhancer sequence (LEN) directed enhanced green fluorescent protein (EGFP) expression in response to larval ventricle regeneration and such activation was attenuated by hemodynamic force alteration and mechanosensation pathway modulation. Further analysis revealed that Notch signaling influenced the endocardial LEN activity as well as endogenous lepb expression. Altogether, our work has established zebrafish models for rapid characterization of cardiac RREs in vivo and provides novel insights on the regulation of LEN by hemodynamic forces and other signaling pathways during heart regeneration.