Knockdown of TNF-α by DNAzyme gold nanoparticles as an anti-inflammatory therapy for myocardial infarction.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 26773660.
- Also identified by DOI 10.1016/j.biomaterials.2015.12.022 and PMC identifier 5564214.
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Abstract
In this study, we used deoxyribozyme (DNAzyme) functionalized gold nanoparticles (AuNPs) to catalytically silence tumor necrosis factor-α (TNF-α) in vivo as a potential therapeutic for myocardial infarction (MI). Using primary macrophages as a model, we demonstrated 50% knockdown of TNF-α, which was not attainable using Lipofectamine-based approaches. Local injection of DNAzyme conjugated to gold particles (AuNPs) in the rat myocardium yielded TNF-α knockdown efficiencies of 50%, which resulted in significant anti-inflammatory effects and improvement in acute cardiac function following MI. Our results represent the first example showing the use of DNAzyme AuNP conjugates in vivo for viable delivery and gene regulation. This is significant as TNF-α is a multibillion dollar drug target implicated in many inflammatory-mediated disorders, thus underscoring the potential impact of DNAzyme-conjugated AuNPs.
Medical subject headings
- Anti-Inflammatory Agents
- DNA, Catalytic
- Gene Knockdown Techniques
- Gold
- Metal Nanoparticles
- Myocardial Infarction
- Tumor Necrosis Factor-alpha