<?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>2026-06-08T04:20:05Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/92186" metadataPrefix="marc">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/92186</identifier><datestamp>2024-01-11T02:43:42Z</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">Valle Noguera, Ana</subfield>
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      <subfield code="a">Sancho Temiño, Lucía</subfield>
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      <subfield code="a">Castillo González, Raquel</subfield>
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      <subfield code="a">Villa Gómez, Cristina</subfield>
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      <subfield code="a">Gomez Sánchez, María José</subfield>
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      <subfield code="a">Ochoa Ramos, Anne</subfield>
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      <subfield code="a">González Granado, José María</subfield>
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      <subfield code="a">Cruz Adalia, Aranzazu</subfield>
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      <subfield code="c">2023-12-26</subfield>
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      <subfield code="a">Group 3 innate lymphoid cells (ILC3s) are vital for defending tissue barriers from invading pathogens. Hypoxia influences the production of intestinal ILC3-derived cytokines by activating HIF. Yet, the mechanisms gov- erning HIF-1a in ILC3s and other innate RORgt+ cells during in vivo infections are poorly understood. In our study, transgenic mice with specific Hif-1a gene inactivation in innate RORgt+ cells (RAG1KO HIF- 1a6Rorc) exhibit more severe colitis following Citrobacter rodentium infection, primarily due to the inability to upregulate IL-22. We find that HIF-1a6Rorc mice have impaired IL-22 production in ILC3s, while non- ILC3 innate RORgt+ cells, also capable of producing IL-22, remain unaffected. Furthermore, we show that IL-18, induced by Toll-like receptor 2, selectively triggers IL-22 in ILC3s by transcriptionally upregulating HIF-1a, revealing an oxygen-independent regulatory pathway. Our results highlight that, during late-stage C. rodentium infection, IL-18 induction in the colon promotes IL-22 through HIF-1a in ILC3s, which is crucial for protection against this pathogen.</subfield>
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      <subfield code="a">Valle-Noguera A, Sancho-Temiño L, Castillo-González R, Villa-Gómez C, Gomez-Sánchez MJ, Ochoa-Ramos A, Yagüe-Fernández P, Soler Palacios B, Zorita V, Raposo-Ponce B, González-Granado JM, Aragonés J, Cruz-Adalia A. IL-18-induced HIF-1α in ILC3s ameliorates the inflammation of C. rodentium-induced colitis. Cell Rep. 2023 Dec 26;42(12):113508. doi: 10.1016/j.celrep.2023.113508. Epub 2023 Nov 28. PMID: 38019650.</subfield>
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      <subfield code="a">2211-1247</subfield>
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      <subfield code="a">10.1016/j.celrep.2023.113508</subfield>
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      <subfield code="a">https://hdl.handle.net/20.500.14352/92186</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">https://www.sciencedirect.com/journal/cell-reports</subfield>
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      <subfield code="a">IL-18-induced HIF-1α in ILC3s ameliorates the inflammation of C. rodentium-induced colitis</subfield>
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