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Lung microRNA Profiling Across the Estrous Cycle in Ozone-exposed Mice
Published on: January 7, 2019
MicroRNA Expression Is Altered in an Ovalbumin-Induced Asthma Model and Targeting miR-155 with Antagomirs Reveals
Maximilian W Plank1, Steven Maltby1, Hock L Tay1
1Centre for Asthma and Respiratory Diseases, School of Biomedical Sciences and Pharmacy, Faculty of Health, University of Newcastle and Hunter Medical Research Institute, Callaghan, NSW 2300, Australia.
Abstract:
MicroRNAs are post-transcriptional regulators of gene expression that are differentially regulated during development and in inflammatory diseases. A role for miRNAs in allergic asthma is emerging and further investigation is required to determine whether they may serve as potential therapeutic targets. We profiled miRNA expression in murine lungs from an ovalbumin-induced allergic airways disease model, and compared expression to animals receiving dexamethasone treatment and non-allergic controls. Our analysis identified 29 miRNAs that were significantly altered during allergic inflammation. Target prediction analysis revealed novel genes with altered expression in allergic airways disease and suggests synergistic miRNA regulation of target mRNAs. To assess the impacts of one induced miRNA on pathology, we targeted miR-155-5p using a specific antagomir. Antagomir administration successfully reduced miR-155-5p expression with high specificity, but failed to alter the disease phenotype. Interestingly, further investigation revealed that antagomir delivery has variable efficacy across different immune cell types, effectively targeting myeloid cell populations, but exhibiting poor uptake in lymphocytes. Our findings demonstrate that antagomir-based targeting of miRNA function in the lung is highly specific, but highlights cell-specificity as a key limitation to be considered for antagomir-based strategies as therapeutics.
Insights
MicroRNAs (miRNAs) are implicated in allergic asthma. Targeting miR-155-5p with antagomirs showed specificity but variable efficacy across immune cells, limiting therapeutic potential in lung disease models.
Area of Science:
- Molecular Biology
- Immunology
- Genetics
Background:
- MicroRNAs (miRNAs) regulate gene expression and are implicated in inflammatory diseases like allergic asthma.
- Understanding miRNA roles is crucial for developing novel therapeutic strategies.
Purpose of the Study:
- To profile miRNA expression in a murine model of allergic airways disease.
- To investigate the therapeutic potential of targeting specific miRNAs, such as miR-155-5p, using antagomirs.
Main Methods:
- Ovalbumin-induced allergic airways disease model in mice.
- miRNA expression profiling in lung tissue.
- Antagomir-mediated inhibition of miR-155-5p.
- Assessment of disease phenotype and antagomir delivery efficacy in immune cells.
Main Results:
- 29 miRNAs were significantly altered in allergic airways disease.
- Antagomir targeting of miR-155-5p reduced its expression specifically.
- Antagomir delivery showed variable efficacy, effectively targeting myeloid cells but not lymphocytes.
- No significant alteration in disease phenotype was observed despite miR-155-5p reduction.
Conclusions:
- Antagomir-based miRNA targeting in the lung is highly specific.
- Cell-specific delivery efficacy is a critical limitation for antagomir-based therapeutics.
- Further strategies are needed to overcome immune cell-specific barriers for effective miRNA-based therapies.
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