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            <subfield code="a">Núñez, D.</subfield>
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            <subfield code="a">A functional analysis on the interspecies interaction between mouse LFA-1 and human intercellular adhesion molecule-1 at the cell level</subfield>
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            <subfield code="c">2017</subfield>
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            <subfield code="a">The interaction between intercellular adhesion molecules (ICAM) and the integrin leukocyte function-associated antigen-1 (LFA-1) is crucial for the regulation of several physiological and pathophysiological processes like cell-mediated elimination of tumor or virus infected cells, cancer metastasis, or inflammatory and autoimmune processes. Using purified proteins it was reported a species restriction for the interaction of ICAM-1 and LFA-1, being mouse ICAM-1 able to interact with human LFA-1 but not human ICAM-1 with mouse LFA-1. However, in vivo results employing tumor cells transfected with human ICAM-1 suggest that functionally mouse LFA-1 can recognize human ICAM-1. In order to clarify the interspecies cross-reactivity of the ICAM-1/LFA-1 interaction, we have performed functional studies analyzing the ability of human soluble ICAM-1 and human/mouse LFA-1 derived peptides to inhibit cell aggregation and adhesion as well as cell-mediated cytotoxicity in both mouse and human systems. In parallel, the affinity of the interaction between mouse LFA-1-derived peptides and human ICAM-1 was determined by calorimetry assays. According to the results obtained, it seems that human ICAM-1 is able to interact with mouse LFA-1 on intact cells, which should be taking into account when using humanized mice and xenograft models for the study of immune-related processes.</subfield>
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            <subfield code="9">info:eu-repo/grantAgreement/ES/MINECO-FEDER/SAF2011-25390</subfield>
            <subfield code="9">info:eu-repo/grantAgreement/ES/MINECO/SAF2014-54763-C2-1-R</subfield>
            <subfield code="9">info:eu-repo/grantAgreement/ES/MINECO/SAF2014-54763-C2-2-R</subfield>
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            <subfield code="a">IMMUNOLOGY</subfield>
            <subfield code="b">30 / 155 = 0.194</subfield>
            <subfield code="c">2017</subfield>
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            <subfield code="a">Immunology and Allergy</subfield>
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            <subfield code="a">Immunology</subfield>
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        <datafield tag="700" ind1=" " ind2=" ">
            <subfield code="a">Comas, L.</subfield>
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            <subfield code="0">(orcid)0000-0001-7328-2094</subfield>
            <subfield code="a">Lanuza, P.M.</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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            <subfield code="a">Sánchez-Martinez, D.</subfield>
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            <subfield code="a">Pérez-Hernández, M.</subfield>
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            <subfield code="a">Catalán, E.</subfield>
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            <subfield code="a">Domingo, M.P.</subfield>
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            <subfield code="0">(orcid)0000-0001-5702-4538</subfield>
            <subfield code="a">Velázquez-Campoy, A.</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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            <subfield code="0">(orcid)0000-0003-0154-0730</subfield>
            <subfield code="a">Pardo, J.</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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            <subfield code="a">Gálvez, E.M.</subfield>
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            <subfield code="1">1008</subfield>
            <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">1002</subfield>
            <subfield code="2">060</subfield>
            <subfield code="a">Universidad de Zaragoza</subfield>
            <subfield code="b">Dpto. Bioq.Biolog.Mol. Celular</subfield>
            <subfield code="c">Área Bioquímica y Biolog.Mole.</subfield>
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            <subfield code="g">8, DEC (2017), 817 [12 pp]</subfield>
            <subfield code="p">Front. immunol.</subfield>
            <subfield code="t">Frontiers in Immunology</subfield>
            <subfield code="x">1664-3224</subfield>
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