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    <subfield code="a">10.1177/2050640617727180</subfield>
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    <subfield code="a">ART-2018-102262</subfield>
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    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Latorre, E.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-5797-3909</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Toll-like receptors 2 and 4 modulate intestinal IL-10 differently in ileum and colon</subfield>
  </datafield>
  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2018</subfield>
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  <datafield tag="506" ind1="0" ind2=" ">
    <subfield code="a">Access copy available to the general public</subfield>
    <subfield code="f">Unrestricted</subfield>
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  <datafield tag="520" ind1="3" ind2=" ">
    <subfield code="a">Background: Inflammatory bowel diseases are consequence of an intestinal homeostasis breakdown in which innate immune dysregulation is implicated. Toll-like receptor (TLR)2 and TLR4 are immune recognition receptors expressed in the intestinal epithelium, the first physical-physiological barrier for microorganisms, to inform the host of the presence of Gram-positive and Gram-negative organisms. Interleukin (IL)-10 is an essential anti-inflammatory cytokine that contributes to maintenance of intestinal homeostasis. Aim: Our main aim was to investigate intestinal IL-10 synthesis and release, and whether TLR2 and TLR4 are determinants of IL-10 expression in the intestinal tract. Methods: We used Caco-2 cell line as an enterocyte-like cell model, and also ileum and colon from mice deficient in TLR2, TLR4 or TLR2/4 to test the involvement of TLR signaling. Results: Intestinal epithelial cells are able to synthesize and release IL-10 and their expression is increased after TLR2 or TLR4 activation. IL-10 regulation seems to be tissue specific, with IL-10 expression in the ileum regulated by a compensation between TLR2 and TLR4 expression, whereas in the colon, TLR2 and TLR4 affect IL-10 expression independently. Conclusions: Intestinal epithelial cells could release IL-10 in response to TLR activation, playing an intestinal tissue-dependent and critical intestinal immune role.</subfield>
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    <subfield code="9">info:eu-repo/grantAgreement/ES/DGA/B61</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/MICINN-FEDER/BFU2010-18971</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/UZ/2014-BIO-03</subfield>
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    <subfield code="9">info:eu-repo/semantics/openAccess</subfield>
    <subfield code="a">All rights reserved</subfield>
    <subfield code="u">http://www.europeana.eu/rights/rr-f/</subfield>
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  <datafield tag="590" ind1=" " ind2=" ">
    <subfield code="a">3.453</subfield>
    <subfield code="b">2018</subfield>
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  <datafield tag="591" ind1=" " ind2=" ">
    <subfield code="a">GASTROENTEROLOGY &amp; HEPATOLOGY</subfield>
    <subfield code="b">33 / 84 = 0.393</subfield>
    <subfield code="c">2018</subfield>
    <subfield code="d">Q2</subfield>
    <subfield code="e">T2</subfield>
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  <datafield tag="592" ind1=" " ind2=" ">
    <subfield code="a">1.329</subfield>
    <subfield code="b">2018</subfield>
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  <datafield tag="593" ind1=" " ind2=" ">
    <subfield code="a">Oncology</subfield>
    <subfield code="c">2018</subfield>
    <subfield code="d">Q1</subfield>
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  <datafield tag="593" ind1=" " ind2=" ">
    <subfield code="a">Gastroenterology</subfield>
    <subfield code="c">2018</subfield>
    <subfield code="d">Q1</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Layunta, E.</subfield>
    <subfield code="0">(orcid)0000-0001-5573-6144</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Grasa, L.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-5306-9365</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Pardo, J.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-0154-0730</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">García, S.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-3970-5457</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Alcalde, A. I.</subfield>
    <subfield code="0">(orcid)0000-0002-9935-927X</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Mesonero, J. E.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-4758-3998</subfield>
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    <subfield code="1">1005</subfield>
    <subfield code="2">410</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Farmacología y Fisiolog.</subfield>
    <subfield code="c">Área Fisiología</subfield>
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    <subfield code="2">566</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Microb.Med.Pr.,Sal.Públ.</subfield>
    <subfield code="c">Área Inmunología</subfield>
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    <subfield code="1">1007</subfield>
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    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Medicina, Psiqu. y Derm.</subfield>
    <subfield code="c">Area Medicina</subfield>
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    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Bioq.Biolog.Mol. Celular</subfield>
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    <subfield code="g">6, 3 (2018), 446-453</subfield>
    <subfield code="p">United European Gastroenterol. j.</subfield>
    <subfield code="t">United European Gastroenterology Journal</subfield>
    <subfield code="x">2050-6406</subfield>
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