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Endothelial cells LEENE on noncoding RNAs in diabetic vasculopathy
Long noncoding RNAs (lncRNAs) have emerged as key mediators of regulated gene expression in diverse biologic contexts, including cardiovascular disease. In this issue of the JCI, Tang, Luo, and colleagues explored the contributions of lncRNAs in diabetic vasculopathy. The authors identified the lncR...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Society for Clinical Investigation
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9888374/ https://www.ncbi.nlm.nih.gov/pubmed/36719373 http://dx.doi.org/10.1172/JCI167047 |
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author | Kallapur, Aneesh Sallam, Tamer |
author_facet | Kallapur, Aneesh Sallam, Tamer |
author_sort | Kallapur, Aneesh |
collection | PubMed |
description | Long noncoding RNAs (lncRNAs) have emerged as key mediators of regulated gene expression in diverse biologic contexts, including cardiovascular disease. In this issue of the JCI, Tang, Luo, and colleagues explored the contributions of lncRNAs in diabetic vasculopathy. The authors identified the lncRNA LEENE as a key mediator of angiogenesis and ischemic response. In a model of diabetic peripheral arterial disease, loss of LEENE led to impaired vascular perfusion, while its overexpression rescued the ischemic defect. The authors used unbiased chromatin affinity assays to decipher LEENE’s interactome and mode of action. These findings offer insights as to why patients with diabetes are uniquely susceptible to developing peripheral vascular disease and fill important gaps in our understanding of mechanisms that connect metabolic dysregulation with impaired angiogenesis. |
format | Online Article Text |
id | pubmed-9888374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Clinical Investigation |
record_format | MEDLINE/PubMed |
spelling | pubmed-98883742023-02-06 Endothelial cells LEENE on noncoding RNAs in diabetic vasculopathy Kallapur, Aneesh Sallam, Tamer J Clin Invest Commentary Long noncoding RNAs (lncRNAs) have emerged as key mediators of regulated gene expression in diverse biologic contexts, including cardiovascular disease. In this issue of the JCI, Tang, Luo, and colleagues explored the contributions of lncRNAs in diabetic vasculopathy. The authors identified the lncRNA LEENE as a key mediator of angiogenesis and ischemic response. In a model of diabetic peripheral arterial disease, loss of LEENE led to impaired vascular perfusion, while its overexpression rescued the ischemic defect. The authors used unbiased chromatin affinity assays to decipher LEENE’s interactome and mode of action. These findings offer insights as to why patients with diabetes are uniquely susceptible to developing peripheral vascular disease and fill important gaps in our understanding of mechanisms that connect metabolic dysregulation with impaired angiogenesis. American Society for Clinical Investigation 2023-02-01 /pmc/articles/PMC9888374/ /pubmed/36719373 http://dx.doi.org/10.1172/JCI167047 Text en © 2023 Kallapur1 et al. https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Commentary Kallapur, Aneesh Sallam, Tamer Endothelial cells LEENE on noncoding RNAs in diabetic vasculopathy |
title | Endothelial cells LEENE on noncoding RNAs in diabetic vasculopathy |
title_full | Endothelial cells LEENE on noncoding RNAs in diabetic vasculopathy |
title_fullStr | Endothelial cells LEENE on noncoding RNAs in diabetic vasculopathy |
title_full_unstemmed | Endothelial cells LEENE on noncoding RNAs in diabetic vasculopathy |
title_short | Endothelial cells LEENE on noncoding RNAs in diabetic vasculopathy |
title_sort | endothelial cells leene on noncoding rnas in diabetic vasculopathy |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9888374/ https://www.ncbi.nlm.nih.gov/pubmed/36719373 http://dx.doi.org/10.1172/JCI167047 |
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