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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.3389/fimmu.2017.01817</dc:identifier><dc:language>eng</dc:language><dc:creator>Núñez, D.</dc:creator><dc:creator>Comas, L.</dc:creator><dc:creator>Lanuza, P.M.</dc:creator><dc:creator>Sánchez-Martinez, D.</dc:creator><dc:creator>Pérez-Hernández, M.</dc:creator><dc:creator>Catalán, E.</dc:creator><dc:creator>Domingo, M.P.</dc:creator><dc:creator>Velázquez-Campoy, A.</dc:creator><dc:creator>Pardo, J.</dc:creator><dc:creator>Gálvez, E.M.</dc:creator><dc:title>A functional analysis on the interspecies interaction between mouse LFA-1 and human intercellular adhesion molecule-1 at the cell level</dc:title><dc:identifier>ART-2017-104253</dc:identifier><dc:description>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.</dc:description><dc:date>2017</dc:date><dc:source>http://zaguan.unizar.es/record/65321</dc:source><dc:doi>10.3389/fimmu.2017.01817</dc:doi><dc:identifier>http://zaguan.unizar.es/record/65321</dc:identifier><dc:identifier>oai:zaguan.unizar.es:65321</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/FSE</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO/BFU2016-78232-P</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO-FEDER/SAF2011-25390</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO/SAF2014-54763-C2-1-R</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO/SAF2014-54763-C2-2-R</dc:relation><dc:identifier.citation>Frontiers in Immunology 8, DEC (2017), 817 [12 pp]</dc:identifier.citation><dc:rights>by</dc:rights><dc:rights>http://creativecommons.org/licenses/by/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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