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In Vivo Nanovector Delivery of a Heart-specific MicroRNA-sponge
Published on: June 15, 2018
Extracellular vesicular MicroRNA-27a* contributes to cardiac hypertrophy in chronic heart failure
Changhai Tian1, Guoku Hu2, Lie Gao1
1Department of Cellular and Integrative Physiology, University of Nebraska Medical Center, Omaha, NE 68198-5850, United States of America.
Abstract:
Under stress, the heart undergoes extensive remodeling resulting in cardiac fibrosis and hypertrophy, ultimately contributing to chronic heart failure (CHF). Alterations in microRNA levels are associated with dysfunctional gene expression profiles involved in the pathogenesis of heart failure. We previously showed that myocardial infarction-induced microRNA-enriched extracellular vesicles (EVs) contribute to the reduction in antioxidant enzymes by targeting Nrf2 signaling in CHF. MicroRNA-27a (miRNA-27a) is the predominant microRNA contained in cardiac fibroblast-derived EVs contributing to oxidative stress along with hypertrophic gene expression in cardiomyocytes. In the present study, we observed that miRNA-27a passenger strand (miRNA-27a*) was markedly upregulated in the non-infarcted area of the left ventricle of rats with CHF and encapsulated into EVs and secreted into the circulation. Bioinformatic analysis revealed that PDZ and LIM domain 5 (PDLIM5) is one of the major targets of miRNA-27a*, playing a major role in cardiac structure and function, and potentially contributing to the progression of cardiac hypertrophy. Our in vivo data demonstrate that PDLIM5 is down-regulated in the progression of heart failure, accompanied with the upregulation of hypertrophic genes and consistent with alterations in miRNA-27a*. Moreover, exogenous administration of miRNA27a* mimics inhibit PDLIM5 translation in cardiomyocytes whereas a miRNA27a* inhibitor enhanced PDLIM5 expression. Importantly, we confirmed that infarcted hearts have higher abundance of miRNA-27a* in EVs compared to normal hearts and further demonstrated that cultured cardiac fibroblasts secrete miRNA27a*-enriched EVs into the extracellular space in response to Angiotensin II stimulation, which inhibited PDLIM5 translation, leading to cardiomyocyte hypertrophic gene expression. In vivo studies suggest that the administration of a miRNA-27a* inhibitor in CHF rats partially blocks endogenous miR-27a* expression, prevents hypertrophic gene expression and improves myocardial contractility. These findings suggest that cardiac fibroblast-secretion of miRNA27a*-enriched EVs may act as a paracrine signaling mediator of cardiac hypertrophy that has potential as a novel therapeutic target.
Insights
Cardiac fibroblast extracellular vesicles (EVs) carrying microRNA-27a* promote heart hypertrophy by targeting PDLIM5. Inhibiting this microRNA-27a* in EVs may offer a novel therapeutic strategy for chronic heart failure (CHF).
Area of Science:
- Cardiovascular Biology
- Molecular Cardiology
- Extracellular Vesicle Biology
Background:
- Chronic heart failure (CHF) involves cardiac remodeling, fibrosis, and hypertrophy, often linked to altered microRNA (miRNA) levels.
- MicroRNA-enriched extracellular vesicles (EVs) from infarcted hearts contribute to heart failure pathogenesis by targeting key signaling pathways.
- Cardiac fibroblast-derived EVs containing miRNA-27a (miRNA-27a) are implicated in oxidative stress and cardiomyocyte hypertrophy.
Purpose of the Study:
- To investigate the role of miRNA-27a passenger strand (miRNA-27a*) in cardiac hypertrophy and its potential as a therapeutic target in chronic heart failure (CHF).
- To identify the molecular targets of miRNA-27a* and elucidate its mechanism of action in cardiac remodeling.
Main Methods:
- Analysis of miRNA-27a* and PDLIM5 expression in rat hearts with CHF.
- Bioinformatic analysis to predict miRNA-27a* targets.
- In vitro studies using cardiomyocytes and cardiac fibroblasts to assess the effects of miRNA-27a* mimics and inhibitors on PDLIM5 translation and hypertrophic gene expression.
- In vivo administration of a miRNA-27a* inhibitor in CHF rats to evaluate its therapeutic potential.
Main Results:
- miRNA-27a* was upregulated in the non-infarcted area of CHF rat hearts, encapsulated in EVs, and secreted into circulation.
- PDLIM5, a key regulator of cardiac structure, was identified as a target of miRNA-27a* and was downregulated in CHF.
- Cardiac fibroblasts secreted miRNA27a*-enriched EVs upon Angiotensin II stimulation, inhibiting PDLIM5 and promoting cardiomyocyte hypertrophy.
- In vivo administration of a miRNA-27a* inhibitor in CHF rats partially reversed these effects, improving myocardial contractility.
Conclusions:
- Cardiac fibroblast-derived EVs carrying miRNA-27a* act as paracrine mediators of cardiac hypertrophy.
- Targeting miRNA-27a* within EVs presents a novel therapeutic strategy for mitigating cardiac hypertrophy and potentially treating chronic heart failure.
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