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    <subfield code="a">10.1177/2050640616663689</subfield>
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    <subfield code="a">Layunta, E.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0001-5573-6144</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Toll-like receptor 9 modifies intestinal serotonergic system.</subfield>
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    <subfield code="c">2016</subfield>
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    <subfield code="a">Introduction: Toll-like receptor 9 (TLR9) is expressed in intestinal epithelial cells, which recognize microbiota developing different responses 1. Several studies have shown that TLR9 seems to be involved in Inflammatory Bowel Diseases (IBD) due to an inappropriate defensive response against microorganisms 2. Moreover, intestinal serotonergic system is also altered in IBD, where extracellular serotonin (5–HT) levels are increased 3. 5-HT bioavailability is mainly regulated by the serotonin transporter (SERT), expressed in enterocytes 4. Aims &amp; Methods: The aim of the present study was to analyse whether TLR9 activation affects SERT expression and activity, and expression of other elements from the serotonergic system (TPH1, TPH2 and 5-HT receptors). Human enterocyte-like Caco-2 cells, and ileum and colon from TLR9-/- mice and Dextran Sulphate Sodium (DSS) mouse colitis model were used as experimental models. mRNA expression was determined by RT-qPCR, and protein expression by western blot...</subfield>
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    <subfield code="9">info:eu-repo/semantics/openAccess</subfield>
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    <subfield code="a">3.673</subfield>
    <subfield code="b">2016</subfield>
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    <subfield code="a">GASTROENTEROLOGY &amp; HEPATOLOGY</subfield>
    <subfield code="b">21 / 79 = 0.266</subfield>
    <subfield code="c">2016</subfield>
    <subfield code="d">Q2</subfield>
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    <subfield code="a">Oncology</subfield>
    <subfield code="c">2016</subfield>
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    <subfield code="a">Gastroenterology</subfield>
    <subfield code="c">2016</subfield>
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    <subfield code="a">Latorre, E.</subfield>
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    <subfield code="a">Forcén, R.</subfield>
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    <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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    <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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    <subfield code="a">Castro, M.</subfield>
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    <subfield code="a">Plaza, M.A.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-7412-2073</subfield>
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    <subfield code="a">Arruebo, M.P.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-2114-0577</subfield>
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    <subfield code="a">Mesonero, J.E.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
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    <subfield code="1">1005</subfield>
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    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Farmacología y Fisiolog.</subfield>
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    <subfield code="1">1008</subfield>
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    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Microb.Med.Pr.,Sal.Públ.</subfield>
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    <subfield code="g">4, Suppl. 1 (2016), A426-A426</subfield>
    <subfield code="p">United European Gastroenterol. j.</subfield>
    <subfield code="t">United European Gastroenterology Journal</subfield>
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