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    <subfield code="a">10.1016/j.celrep.2021.108757</subfield>
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    <subfield code="2">sideral</subfield>
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    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <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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    <subfield code="a">IL-22 promotes the formation of a MUC17 glycocalyx barrier in the postnatal small intestine during weaning</subfield>
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    <subfield code="c">2021</subfield>
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    <subfield code="a">The intestine is under constant exposure to chemicals, antigens, and microorganisms from the external environment. Apical aspects of transporting epithelial cells (enterocytes) form a brush-border membrane (BBM), shaped by packed microvilli coated with a dense glycocalyx. We present evidence showing that the glycocalyx forms an epithelial barrier that prevents exogenous molecules and live bacteria from gaining access to BBM. We use a multi-omics approach to investigate the function and regulation of membrane mucins exposed on the BBM during postnatal development of the mouse small intestine. Muc17 is identified as a major membrane mucin in the glycocalyx that is specifically upregulated by IL-22 as part of an epithelial defense repertoire during weaning. High levels of IL-22 at time of weaning reprogram neonatal postmitotic progenitor enterocytes to differentiate into Muc17-expressing enterocytes, as found in the adult intestine during homeostasis. Our findings propose a role for Muc17 in epithelial barrier function in the small intestine.</subfield>
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    <subfield code="a">CELL BIOLOGY</subfield>
    <subfield code="b">33 / 195 = 0.169</subfield>
    <subfield code="c">2021</subfield>
    <subfield code="d">Q1</subfield>
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    <subfield code="a">4.845</subfield>
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    <subfield code="a">Biochemistry, Genetics and Molecular Biology (miscellaneous)</subfield>
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    <subfield code="a">Jäverfelt, S.</subfield>
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    <subfield code="a">Dolan, B.</subfield>
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    <subfield code="a">Arike, L.</subfield>
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    <subfield code="a">Pelaseyed, T.</subfield>
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    <subfield code="1">1012</subfield>
    <subfield code="2">410</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Farmac.Fisiol.y Med.L.F.</subfield>
    <subfield code="c">Área Fisiología</subfield>
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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">34, 7 (2021), 108757 [24 pp.]</subfield>
    <subfield code="p">Cell Reports</subfield>
    <subfield code="t">Cell Reports</subfield>
    <subfield code="x">2211-1247</subfield>
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