<?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>2026-08-05T11:42:07Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/10712" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/10712</identifier><datestamp>2024-09-27T08:04:57Z</datestamp><setSpec>com_20.500.12105_19604</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_19605</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">López, Esther</subfield>
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      <subfield code="a">Marinaro, Federica</subfield>
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      <subfield code="a">de Pedro, María de Los Ángeles</subfield>
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      <subfield code="a">Sánchez-Margallo, Francisco Miguel</subfield>
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      <subfield code="a">Gomez-Serrano, Maria</subfield>
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      <subfield code="a">Ponath, Viviane</subfield>
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      <subfield code="a">Pogge von Strandmann, Elke</subfield>
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      <subfield code="a">Jorge, Inmaculada</subfield>
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      <subfield code="a">Vazquez, Jesus</subfield>
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      <subfield code="a">Fernández-Pereira, Luis Miguel</subfield>
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      <subfield code="a">Crisóstomo, Verónica</subfield>
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      <subfield code="a">Alvarez, Veronica</subfield>
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      <subfield code="a">Casado, Javier G</subfield>
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      <subfield code="c">2020-06</subfield>
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      <subfield code="a">Experimental data demonstrated that the regenerative potential and immunomodulatory capacity of cardiosphere-derived cells (CDCs) is mediated by paracrine mechanisms. In this process, extracellular vesicles derived from CDCs (EV-CDCs) are key mediators of their therapeutic effect. Considering the future applicability of these vesicles in human diseases, an accurate preclinical-to-clinical translation is needed, as well as an exhaustive molecular characterization of animal-derived therapeutic products. Based on that, the main goal of this study was to perform a comprehensive characterization of proteins and miRNAs in extracellular vesicles from porcine CDCs as a clinically relevant animal model. The analysis was performed by identification and quantification of proteins and miRNA expression profiles. Our results revealed the presence of clusters of immune-related and cardiac-related molecular biomarkers in EV-CDCs. Additionally, considering that priming stem cells with inflammatory stimuli may increase the therapeutic potential of released vesicles, here we studied the dynamic changes that occur in the extracellular vesicles from IFNγ-primed CDCs. These analyses detected statistically significant changes in several miRNAs and proteins. Notably, the increase in interleukin 6 (IL6) protein, as well as the increase in mir-125b (that targets IL6 receptor) was especially relevant. These results suggest a potential involvement of EV-CDCs in the regulation of the IL6/IL6R axis, with implications in inflammatory-mediated diseases.</subfield>
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      <subfield code="a">Front Cell Dev Biol. 2020; 8:321</subfield>
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      <subfield code="a">Frontiers in cell and developmental biology</subfield>
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      <subfield code="a">32582685</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/10712</subfield>
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      <subfield code="a">The Immunomodulatory Signature of Extracellular Vesicles From Cardiosphere-Derived Cells: A Proteomic and miRNA Profiling.</subfield>
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