Related Experiment Video
Updated: Dec 10, 2025

In Vivo Nanovector Delivery of a Heart-specific MicroRNA-sponge
Published on: June 15, 2018
MicroRNA-183 as a Novel Regulator Protects Against Cardiomyocytes Hypertrophy via Targeting TIAM1
Fu-Han Gong1, Xi-Lu Chen2, Quan Zhang3
1Department of Cardiology, Tongren Municipal People's Hospital, Tongren, China.
Background:
MicroRNAs serve as important regulators of the pathogenesis of cardiac hypertrophy. Among them, miR-183 is well documented as a novel tumor suppressor in previous studies, whereas it exhibits a downregulated expression in cardiac hypertrophy recently. The present study was aimed to examine the effect of miR-183 on cardiomyocytes hypertrophy.
Methods:
Angiotensin II (Ang II) was used for establishment of cardiac hypertrophy model in vitro. Neonatal rat ventricular cardiomyocytes transfected with miR-183 mimic or negative control were further utilized for the phenotype analysis. Moreover, the bioinformatics analysis and luciferase reporter assays were used for exploring the potential target of miR-183 in cardiomyocytes.
Results:
We observed a significant decreased expression of miR-183 in hypertrophic cardiomyocytes. Overexpression of miR-183 significantly attenuated the cardiomyocytes size morphologically and prohypertrophic genes expression. Moreover, we demonstrated that TIAM1 was a direct target gene of miR-183 verified by bioinformatics analysis and luciferase reporter assays, which showed a decreased mRNA and protein expression in the cardiomyocytes transfected with miR-183 upon Ang II stimulation. Additionally, the downregulated TIAM1 expression was required for the attenuated effect of miR-183 on cardiomyocytes hypertrophy.
Conclusions:
Taken together, these evidences indicated that miR-183 acted as a cardioprotective regulator for the development of cardiomyocytes hypertrophy via directly regulation of TIAM1.
Insights
MicroRNA-183 (miR-183) is downregulated in cardiac hypertrophy. Restoring miR-183 levels protects against heart cell enlargement by targeting TIAM1, offering a potential therapeutic strategy.
Area of Science:
- Cardiovascular Biology
- Molecular Cardiology
- Epigenetics
Background:
- MicroRNAs regulate cardiac hypertrophy pathogenesis.
- miR-183, known as a tumor suppressor, is downregulated in cardiac hypertrophy.
Purpose of the Study:
- To investigate the role of miR-183 in cardiomyocyte hypertrophy.
- To identify the molecular targets of miR-183 in the context of cardiac hypertrophy.
Main Methods:
- Cardiac hypertrophy model induced by Angiotensin II (Ang II) in vitro.
- Transfection of neonatal rat ventricular cardiomyocytes with miR-183 mimic.
- Bioinformatics analysis and luciferase reporter assays to identify miR-183 targets.
Main Results:
- miR-183 expression was significantly decreased in hypertrophic cardiomyocytes.
- Overexpression of miR-183 attenuated cardiomyocyte size and prohypertrophic gene expression.
- TIAM1 was identified as a direct target of miR-183, with its expression reduced by miR-183 mimic transfection.
Conclusions:
- miR-183 acts as a cardioprotective regulator in cardiac hypertrophy.
- The protective effect of miR-183 is mediated through direct regulation of TIAM1.
More Related Videos
08:22Tissue-specific miRNA Expression Profiling in Mouse Heart Sections Using In Situ Hybridization
Published on: September 15, 2018
09:16Suppression of Pro-fibrotic Signaling Potentiates Factor-mediated Reprogramming of Mouse Embryonic Fibroblasts into Induced Cardiomyocytes
Published on: June 3, 2018
Related Concept Videos
MicroRNAs
MicroRNAs
Cardiomyopathy III: Hypertrophic Cardiomyopathy
mTOR Signaling and Cancer Progression
The mTOR pathway or the...