<?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>2026-06-29T01:18:29Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/17925" metadataPrefix="marc">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/17925</identifier><datestamp>2024-09-16T15:50:44Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Valencia Mahón, Jaris</subfield>
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      <subfield code="a">Jiménez Pérez, Eva</subfield>
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      <subfield code="a">Martínez, Víctor G.</subfield>
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      <subfield code="a">Amo, Beatriz G. del</subfield>
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      <subfield code="a">Hidalgo, Laura</subfield>
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      <subfield code="a">Entrena Martínez, Ana</subfield>
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      <subfield code="a">Martínez Fernández De Sevilla, Lidia</subfield>
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      <subfield code="a">Río Gallegos, Francisco José Del</subfield>
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      <subfield code="a">Varas Fajardo, Alberto</subfield>
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      <subfield code="a">Vicente López, María Ángeles</subfield>
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      <subfield code="a">Sacedón Ayuso, Rosa</subfield>
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      <subfield code="c">2017</subfield>
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      <subfield code="a">Fibroblastic reticular cells (FRCs) are essential players during adaptive immune responses not only as a structural support for the encounter of antigen-presenting cells and naive T lymphocytes but also as a source of modulatory signals. However, little is known about this cell population in humans. To address the phenotypical and functional analysis of human FRCs here we established splenic (SP) and mesenteric lymph node (LN) CD45- CD31- CD90+ podoplanin+ myofibroblastic cell cultures.They shared the phenotypical characteristics distinctive of FRCs, including the expression of immunomodulatory factors and peripheral tissue antigens. Nevertheless, human FRCs also showed particular features, some differing from mouse FRCs, like the lack of nitric oxide synthase (NOS2) expression after interferon (IFN)γstimulation. Interestingly, SP-FRCs expressed higher levels of interleukin (IL)-6, BMP4, CCL2, CXCL12 and Notch molecules, and strongly adapted their functional profile to lipopolysaccharide (LPS), polyinosinic:polycytidylic acid (Poly I:C) and IFNγ stimulation. In contrast, we found higher expression of transforming growth factor (TGF)β and Activin A in LN-FRCs that barely responded via Toll-Like Receptor (TLR)3 and constitutively expressed retinaldehyde dehydrogenase 1 enzyme, absent in SP-FRCs. This study reveals human FRCs can be valuable models to increase our knowledge about the physiology of human secondary lymphoid organs in health and disease and to explore the therapeutic options of FRCs.</subfield>
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      <subfield code="a">Valencia Mahón, J., Jiménez Pérez, E., Martínez, V. G. et al. «Characterization of Human Fibroblastic Reticular Cells as Potential Immunotherapeutic Tools». Cytotherapy, vol. 19, n.o 5, mayo de 2017, pp. 640-53. DOI.org (Crossref), https://doi.org/10.1016/j.jcyt.2017.01.010.</subfield>
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      <subfield code="a">10.1016/j.jcyt.2017.01.010</subfield>
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      <subfield code="a">https://hdl.handle.net/20.500.14352/17925</subfield>
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      <subfield code="a">https//doi.org/10.1016/j.jcyt.2017.01.010</subfield>
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      <subfield code="a">http://www.tandfonline.com/toc/icyt20/current</subfield>
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      <subfield code="a">Characterization of human fibroblastic reticular cells as potential immunotherapeutic tools</subfield>
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