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Updated: Apr 19, 2026

NF-κB-dependent Luciferase Activation and Quantification of Gene Expression in Salmonella Infected Tissue Culture Cells
Published on: January 12, 2020
Noncoding RNAs regulate NF-κB signaling to modulate blood vessel inflammation
Henry S Cheng1, Makon-Sébastien Njock1, Nadiya Khyzha1
1Toronto General Research Institute, University Health Network Toronto, ON, Canada ; Department of Laboratory Medicine and Pathobiology, University of Toronto Toronto, ON, Canada ; Heart and Stroke/Richard Lewar Centre of Excellence in Cardiovascular Research Toronto, ON, Canada.
Insights
Vascular inflammation, driven by NF-κB signaling, contributes to atherosclerosis. MicroRNAs regulate this pathway, offering potential therapeutic targets for cardiovascular disease and aging.
Area of Science:
- Cardiovascular Biology
- Molecular Medicine
- Aging Research
Background:
- Cardiovascular diseases, including atherosclerosis, are major global health burdens.
- Atherosclerosis progression is linked to vascular inflammation and endothelial cell activation.
- The transcription factor NF-κB is central to endothelial inflammatory signaling, with enhanced activity during aging.
Purpose of the Study:
- To review the role of microRNAs in regulating vascular inflammation and NF-κB signaling.
- To explore the therapeutic potential of microRNA-based interventions for cardiovascular diseases.
- To discuss emerging roles of long noncoding RNAs and circulating microRNAs in vascular health.
Main Methods:
- Literature review of studies on microRNAs, NF-κB signaling, and vascular inflammation.
- Analysis of data from mouse models of vascular inflammation and atherosclerosis.
- Synthesis of current knowledge on noncoding RNA regulation in endothelial cells.
Main Results:
- Noncoding RNAs, especially microRNAs, significantly modulate the NF-κB signaling pathway in vascular inflammation.
- Dysregulation of these microRNAs is implicated in the pathogenesis of atherosclerosis.
- Aging exacerbates NF-κB activation, potentially mediated by altered noncoding RNA expression.
Conclusions:
- MicroRNAs are key regulators of vascular inflammation and NF-κB activity.
- Targeting microRNA pathways presents a promising therapeutic strategy for atherosclerosis and age-related cardiovascular disease.
- Further research into long noncoding RNAs and circulating microRNAs may reveal novel therapeutic avenues.
Abstract:
Cardiovascular diseases such as atherosclerosis are one of the leading causes of morbidity and mortality worldwide. The clinical manifestations of atherosclerosis, which include heart attack and stroke, occur several decades after initiation of the disease and become more severe with age. Inflammation of blood vessels plays a prominent role in atherogenesis. Activation of the endothelium by inflammatory mediators leads to the recruitment of circulating inflammatory cells, which drives atherosclerotic plaque formation and progression. Inflammatory signaling within the endothelium is driven predominantly by the pro-inflammatory transcription factor, NF-κB. Interestingly, activation of NF-κB is enhanced during the normal aging process and this may contribute to the development of cardiovascular disease. Importantly, studies utilizing mouse models of vascular inflammation and atherosclerosis are uncovering a network of noncoding RNAs, particularly microRNAs, which impinge on the NF-κB signaling pathway. Here we summarize the literature regarding the control of vascular inflammation by microRNAs, and provide insight into how these microRNA-based pathways might be harnessed for therapeutic treatment of disease. We also discuss emerging areas of endothelial cell biology, including the involvement of long noncoding RNAs and circulating microRNAs in the control of vascular inflammation.
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