Circular RNA IGF1R Promotes Cardiac Repair via Activating β-Catenin Signaling by Interacting with DDX5 in Mice after Ischemic Insults.
Tian-Kai ShanTong-Tong YangPeng JingYu-Lin BaoLiu-Hua ZhouTing ZhuXin-Ying ShiTian-Wen WeiSi-Bo WangLing-Feng GuJia-Wen ChenYe HeZe-Mu WangQi-Ming WangLi-Ping XieAi-Hua GuYang ZhaoYong JiHao WangLian-Sheng WangPublished in: Research (Washington, D.C.) (2024)
The potential of circular RNAs (circRNAs) as biomarkers and therapeutic targets is becoming increasingly evident, yet their roles in cardiac regeneration and myocardial renewal remain largely unexplored. Here, we investigated the function of circIGF1R and related mechanisms in cardiac regeneration. Through analysis of circRNA sequencing data from neonatal and adult cardiomyocytes, circRNAs associated with regeneration were identified. Our data showed that circIGF1R expression was high in neonatal hearts, decreased with postnatal maturation, and up-regulated after cardiac injury. The elevation was validated in patients diagnosed with acute myocardial infarction (MI) within 1 week. In human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) and myocardial tissue from mice after apical resection and MI, we observed that circIGF1R overexpression enhanced cardiomyocyte proliferation, reduced apoptosis, and mitigated cardiac dysfunction and fibrosis, while circIGF1R knockdown impeded endogenous cardiac renewal. Mechanistically, we identified circIGF1R binding proteins through circRNA precipitation followed by mass spectrometry. RNA pull-down Western blot and RNA immunoprecipitation demonstrated that circIGF1R directly interacted with DDX5 and augmented its protein level by suppressing ubiquitin-dependent degradation. This subsequently triggered the β-catenin signaling pathway, leading to the transcriptional activation of cyclin D1 and c-Myc. The roles of circIGF1R and DDX5 in cardiac regeneration were further substantiated through site-directed mutagenesis and rescue experiments. In conclusion, our study highlights the pivotal role of circIGF1R in facilitating heart regeneration and repair after ischemic insults. The circIGF1R/DDX5/β-catenin axis emerges as a novel therapeutic target for enhancing myocardial repair after MI, offering promising avenues for the development of regenerative therapies.
Keyphrases
- left ventricular
- stem cells
- acute myocardial infarction
- gene expression
- transcription factor
- cell proliferation
- type diabetes
- small molecule
- oxidative stress
- signaling pathway
- mesenchymal stem cells
- endothelial cells
- crispr cas
- epithelial mesenchymal transition
- skeletal muscle
- big data
- poor prognosis
- clinical trial
- metabolic syndrome
- acute coronary syndrome
- high glucose
- cell cycle
- high resolution
- long non coding rna
- artificial intelligence
- ms ms
- climate change
- ejection fraction
- adipose tissue
- machine learning
- drug induced
- high performance liquid chromatography
- protein protein
- wild type
- electronic health record
- liquid chromatography
- atrial fibrillation
- prognostic factors
- stress induced