<?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>2026-07-18T21:24:50Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/108453" metadataPrefix="rdf">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/108453</identifier><datestamp>2025-03-18T13:22:51Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><rdf:RDF xmlns:rdf="http://www.openarchives.org/OAI/2.0/rdf/" xmlns:ow="http://www.ontoweb.org/ontology/1#" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:ds="http://dspace.org/ds/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/rdf/ http://www.openarchives.org/OAI/2.0/rdf.xsd">
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      <dc:title>Role of Lamin A/C on dendritic cell function in antiviral immunity</dc:title>
      <dc:creator>Herrero-Fernandez, Beatriz</dc:creator>
      <dc:creator>Gómez Bris, Raquel</dc:creator>
      <dc:creator>Ortega-Zapero, Marina</dc:creator>
      <dc:creator>Saez, Angela</dc:creator>
      <dc:creator>Iborra Martín, Salvador</dc:creator>
      <dc:creator>Zorita, Virginia</dc:creator>
      <dc:creator>Quintas, Ana</dc:creator>
      <dc:creator>Vazquez, Enrique</dc:creator>
      <dc:creator>Dopazo, Ana</dc:creator>
      <dc:creator>Sánchez Madrid, Francisco</dc:creator>
      <dc:creator>Arribas, Silvia Magdalena</dc:creator>
      <dc:creator>González Granado, José María</dc:creator>
      <dc:description>Dendritic cells (DCs) play a crucial role in orchestrating immune responses, particularly in promoting IFNγ-producing-CD8 cytotoxic T lymphocytes (CTLs) and IFNγ-producing-CD4 T helper 1 (Th1) cells, which are essential for defending against viral infections. Additionally, the nuclear envelope protein lamin A/C has been implicated in T cell immunity. Nevertheless, the intricate interplay between innate and adaptive immunity in response to viral infections, particularly the role of lamin A/C in DC functions within this context, remains poorly understood. In this study, we demonstrate that mice lacking lamin A/C in myeloid LysM promoter-expressing cells exhibit a reduced capacity to induce Th1 and CD8 CTL responses, leading to impaired clearance of acute primary Vaccinia virus (VACV) infection. Remarkably, in vitro-generated granulocyte macrophage colony-stimulating factor bone marrow-derived DCs (GM-CSF BMDCs) show high levels of lamin A/C. Lamin A/C absence on GM-CSF BMDCs does not affect the expression of costimulatory molecules on the cell membrane but it reduces the cellular ability to form immunological synapses with naïve CD4 T cells. Lamin A/C deletion induces alterations in NFκB nuclear localization, thereby influencing NF-κB-dependent transcription. Furthermore, lamin A/C ablation modifies the gene accessibility of BMDCs, predisposing these cells to mount a less effective antiviral response upon TLR stimulation. This study highlights the critical role of DCs in interacting with CD4 T cells during antiviral responses and proposes some mechanisms through which lamin A/C may modulate DC function via gene accessibility and transcriptional regulation</dc:description>
      <dc:date>2024-09-30T07:09:33Z</dc:date>
      <dc:date>2024-09-30T07:09:33Z</dc:date>
      <dc:date>2024-09-12</dc:date>
      <dc:type>journal article</dc:type>
      <dc:identifier>Herrero-Fernández B, Ortega-Zapero M, Gómez-Bris R, et al. Role of lamin A/C on dendritic cell function in antiviral immunity. Cell Mol Life Sci. 2024;81(1):400. Published 2024 Sep 12. doi:10.1007/s00018-024-05423-9</dc:identifier>
      <dc:identifier>10.1007/s00018-024-05423-9</dc:identifier>
      <dc:identifier>https://hdl.handle.net/20.500.14352/108453</dc:identifier>
      <dc:identifier>https://doi.org/10.1007/s00018-024-05423-9</dc:identifier>
      <dc:identifier>https://link.springer.com/article/10.1007/s00018-024-05423-9</dc:identifier>
      <dc:identifier>https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11393282/</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:relation>info:eu-repo/grantAgreement/ISCIII/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020 (ISCIII)/PI20%2F00306/ES/INMUNOLOGIA, INMUNOPATOLOGIA Y TERAPIA EN ENFERMEDAD INFLAMATORIA INTESTINAL/</dc:relation>
      <dc:relation>info:eu-repo/grantAgreement/MCNU/PID2021/125415OB-I00</dc:relation>
      <dc:relation>info:eu-repo/grantAgreement/MCNU/PID-2020/120412RB-I00</dc:relation>
      <dc:relation>info:eu-repo/grantAgreement/CHRG/LCF/PR/ HR23/52430018</dc:relation>
      <dc:relation>info:eu-repo/grantAgreement/MCNU/FPU18/00895</dc:relation>
      <dc:relation>info:eu-repo/grantAgreement/ISCII/PI24/00146</dc:relation>
      <dc:relation>info:eu-repo/grantAgreement/MCNU/PEJ-2020-TL/BMD- 17604</dc:relation>
      <dc:relation>info:eu-repo/grantAgreement/CAM/LCF/PR/ HR23/52430018</dc:relation>
      <dc:relation>info:eu-repo/grantAgreement/MCNU/FPU19/01774</dc:relation>
      <dc:relation>info:eu-repo/grantAgreement/ISCII/PI20/00306</dc:relation>
      <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
      <dc:rights>open access</dc:rights>
      <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
      <dc:publisher>Springer Nature</dc:publisher>
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