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Background: Electronic-cigarette (e-cig) usage, particularly in the youth population, is a growing concern. It is known that e-cig causes endothelial dysfunction, which is a risk factor for the development of cardiovascular diseases; however, the mechanisms involved remain unclear. We hypothesized that long noncoding RNAs (lncRNAs) may play a role in e-cig-induced endothelial dysfunction.
Methods: Here, we identified lncRNAs that are dysregulated in human induced pluripotent stem cell-derived endothelial cells (iPSC-ECs) following 24 h of e-cig aerosol extract treatment via microarray analysis. We performed Gene Ontology and Kyoto Encyclopedia of Genes and Genome (KEGG) pathway analyses of the dysregulated mRNAs following e-cig exposure and constructed co-expression networks of the top 5 upregulated lncRNAs and the top 5 downregulated lncRNAs and the mRNAs that are correlated with them. Furthermore, the functional effects of knocking down lncRNA lung cancer-associated transcript 1 (LUCAT1) on EC phenotypes were determined as it was one of the significantly upregulated lncRNAs following e-cig exposure based on our profiling.
Results: 183 lncRNAs and 132 mRNAs were found to be upregulated, whereas 297 lncRNAs and 413 mRNAs were found to be downregulated after e-cig exposure. We also observed that e-cig caused dysregulation of endothelial metabolism resulting in increased FAO activity, higher mitochondrial membrane potential, and decreased glucose uptake and glycolysis. These results suggest that e-cig alters EC metabolism by increasing FAO to compensate for energy deficiency in ECs. Finally, the knockdown of LUCAT1 prevented e-cig-induced EC dysfunction by maintaining vascular barrier, reducing reactive oxygen species level, and increasing migration capacity.
Conclusion: This study identifies an expression profile of differentially expressed lncRNAs and several potential regulators and pathways in ECs exposed to e-cig, which provide insights into the regulation of lncRNAs and mRNAs and the role of lncRNA and mRNA networks in ECs associated e-cig exposure.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8643021 | PMC |
http://dx.doi.org/10.1186/s13287-021-02654-6 | DOI Listing |
Semergen
December 2024
Servicio de Neumología, Hospital Universitario de Salamanca, Salamanca, España; Instituto Investigación Biosanitaria de Salamanca, Salamanca, España. Electronic address:
The use of electronic cigarettes and heated tobacco products is increasing among adolescents and young adults. Tobacco companies offer these devices to enhance the smoking experience by magnifying its attractive and minimizing the negatives associated with the consumption of conventional cigarettes. The objective of this review is to update the available knowledge on the impact of these devices, both from an individual perspective, in terms of their effects on health, and from a public health perspective due to direct exposure and the effects derived from the second and third hand emissions.
View Article and Find Full Text PDFHistol Histopathol
November 2024
Centar for Harm Reduction of Biological and Chemical Hazards, Department of Genetics, Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia.
Introduction: Periodontal ligament-derived mesenchymal stem cells (PDL-MSCs) are promising cells with crucial roles in maintaining and repairing periodontal tissue. However, their regenerative capacity can be influenced by various factors, including cigarette smoke and electronic nicotine delivery system (ENDS) aerosols. Smoking and vaping can impair their regenerative potential, and even though ENDS are perceived as safer tobacco products, there is a lack of evidence to guarantee this assumption.
View Article and Find Full Text PDFBehav Pharmacol
December 2024
Department of Biobehavioral Health, Penn State University, University Park, Pennsylvania, USA.
Cigarette smoking is at an all-time low. However, nicotine consumption has diversified with the introduction of commercial tobacco products that include Electronic Nicotine Delivery Systems. Nicotine is the main psychoactive component of tobacco and contributes to the addictive properties of tobacco products.
View Article and Find Full Text PDFSci Rep
December 2024
HMRI Cardiovascular Research Institute, Huntington Medical Research Institutes, 686 South Fair Oaks Avenue, Pasadena, CA, 91105, USA.
J Biochem Mol Toxicol
December 2024
Doctoral Program in Genetics and Molecular Biology, Universidade Federal do Rio Grande do Sul (UFRGS), CEP, Porto Alegre, Brazil.
Smoking, a major behavioral health burden, causes preventable and premature deaths globally. Nicotine, the addictive component present in tobacco products and Electronic cigarettes (E-cigarettes, vape), can bind to nicotinic acetylcholine receptors in the brain to trigger a dopamine release that reinforces smoking. Despite the widespread usage of nicotine, its mechanisms of toxicity, particularly in e-cigarettes, are poorly understood.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!