<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-08T14:02:51Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/92418" metadataPrefix="oai_dc">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/92418</identifier><datestamp>2024-01-12T02:23:00Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   <dc:title>Aging-Associated miR-217 Aggravates Atherosclerosis and Promotes Cardiovascular Dysfunction</dc:title>
   <dc:creator>García-Yébenes Mena, Virginia Pilar</dc:creator>
   <dc:creator>Ramiro, Almudena R.</dc:creator>
   <dc:subject>616.12-005</dc:subject>
   <dc:subject>Endothelial cell</dc:subject>
   <dc:subject>MicroRNAs</dc:subject>
   <dc:subject>Cardiovascular disease</dc:subject>
   <dc:subject>Aging</dc:subject>
   <dc:subject>Ciencias Biomédicas</dc:subject>
   <dc:subject>24 Ciencias de la Vida</dc:subject>
   <dc:description>Objective:microRNAs are master regulators of gene expression with essential roles in virtually all biological processes. miR-217 has been associated with aging and cellular senescence, but its role in vascular disease is not understood.
Approach and Results:We have used an inducible endothelium-specific knock-in mouse model to address the role of miR-217 in vascular function and atherosclerosis. miR-217 reduced NO production and promoted endothelial dysfunction, increased blood pressure, and exacerbated atherosclerosis in proatherogenic apoE−/− mice. Moreover, increased endothelial miR-217 expression led to the development of coronary artery disease and altered left ventricular heart function, inducing diastolic and systolic dysfunction. Conversely, inhibition of endogenous vascular miR-217 in apoE−/− mice improved vascular contractility and diminished atherosclerosis. Transcriptome analysis revealed that miR-217 regulates an endothelial signaling hub and downregulates a network of eNOS (endothelial NO synthase) activators, including VEGF (vascular endothelial growth factor) and apelin receptor pathways, resulting in diminished eNOS expression. Further analysis revealed that human plasma miR-217 is a biomarker of vascular aging and cardiovascular risk.
Conclusions:Our results highlight the therapeutic potential of miR-217 inhibitors in aging-related cardiovascular disease.</dc:description>
   <dc:description>Universidad Complutense de Madrid</dc:description>
   <dc:description>Asociación Española contra el Cáncer</dc:description>
   <dc:description>Depto. de Inmunología, Oftalmología y ORL</dc:description>
   <dc:description>Fac. de Medicina</dc:description>
   <dc:description>TRUE</dc:description>
   <dc:description>pub</dc:description>
   <dc:date>2024-01-11T08:18:04Z</dc:date>
   <dc:date>2024-01-11T08:18:04Z</dc:date>
   <dc:date>2020-10-03</dc:date>
   <dc:type>journal article</dc:type>
   <dc:type>VoR</dc:type>
   <dc:identifier>https://hdl.handle.net/20.500.14352/92418</dc:identifier>
   <dc:identifier>XXXX-XXXX</dc:identifier>
   <dc:identifier>10.1161/ATVBAHA.120.314333</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>RYC-2009-04503</dc:relation>
   <dc:relation>INVES18013GARC</dc:relation>
   <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
   <dc:rights>open access</dc:rights>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>American Heart Association</dc:publisher>
</oai_dc:dc></metadata></record></GetRecord></OAI-PMH>