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Altered thymocyte development observed in EphA4-deficient mice courses with changes in both thymic epithelial and extracellular matrix organization

dc.contributor.authorGarcía Ceca Hernández, Javier
dc.contributor.authorMontero Herradón, Sara
dc.contributor.authorGonzález, Ana
dc.contributor.authorPlaza, Rosa
dc.contributor.authorZapata González, Agustín
dc.date.accessioned2023-06-22T12:28:12Z
dc.date.available2023-06-22T12:28:12Z
dc.date.issued2022-11-05
dc.descriptionCRUE-CSIC (Acuerdos Transformativos 2022)
dc.description.abstractEph receptors and their ligands, Ephrins, are involved in the thymocyte-thymic epithelial cell (TEC) interactions, key for the functional maturation of both thymocytes and thymic epithelium. Several years ago, we reported that the lack of EphA4, a Eph of the subfamily A, coursed with reduced proportions of double positive (DP) thymocytes apparently due to an altered thymic epithelial stroma [Munoz et al. in J Immunol 177:804–813, 2006]. In the present study, we reevaluate the lymphoid, epithelial, and extracellular matrix (ECM) phenotype of EphA4−/− mice grouped into three categories with respect to their proportions of DP thymocytes. Our results demonstrate a profound hypocellularity, specifc alterations of T cell diferentiation that afected not only DP thymocytes, but also double negative and single positive T cell subsets, as well as the proportions of positively and negatively selected thymocytes. In correlation, thymic histological organization changed markedly, especially in the cortex, as well as the proportions of both Ly51+UEA-1− cortical TECs and Ly51−UEA-1+ medullary TECs. The alterations observed in the expression of ECM components (Fibronectin, Laminin, Collagen IV), integrin receptors (VLA-4, VLA-6), chemokines (CXCL12, CCL25, CCL21) and their receptors (CXCR4, CCR7, CCR9) and in vitro transwell assays on the capacity of migration of WT and mutant thymocytes suggest that the lack of EphA4 alters T-cell diferentiation by presumably afecting cell adhesion between TECs and T-TEC interactions rather than by thymocyte migration.
dc.description.departmentDepto. de Biología Celular
dc.description.facultyFac. de Ciencias Biológicas
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Ciencia e Innovación (MICINN)
dc.description.sponsorshipInstituto de Salud Carlos III (ISCIII)
dc.description.sponsorshipComunidad de Madrid
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/75388
dc.identifier.doi10.1007/s00018-022-04610-w
dc.identifier.issn1420-682X
dc.identifier.officialurlhttps://doi.org/10.1007/s00018-022-04610-w
dc.identifier.relatedurlhttps://link.springer.com/article/10.1007/s00018-022-04610-w
dc.identifier.urihttps://hdl.handle.net/20.500.14352/72591
dc.issue.number11
dc.journal.titleCellular and Molecular Life Sciences
dc.language.isoeng
dc.page.final16
dc.page.initial1
dc.publisherSpringer Nature
dc.relation.projectID(RTI2018- 093938-B-I00)
dc.relation.projectID(RD16/0011/0002, Cell Therapy Network, TERCEL; RD21/0017/0010, RICORS TERAV)
dc.relation.projectIDAVANCELL-CM (S2017/BMD-3692)
dc.rightsAtribución 3.0 España
dc.rights.accessRightsopen access
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/es/
dc.subject.cdu577.27
dc.subject.cdu611.438
dc.subject.keywordThymus
dc.subject.keywordEph tyrosine kinase receptors
dc.subject.keywordThymic microenvironments
dc.subject.keywordCell migration
dc.subject.ucmInmunología
dc.subject.ucmBiología celular (Biología)
dc.subject.unesco2412 Inmunología
dc.subject.unesco2407 Biología Celular
dc.titleAltered thymocyte development observed in EphA4-deficient mice courses with changes in both thymic epithelial and extracellular matrix organization
dc.typejournal article
dc.volume.number79
dspace.entity.typePublication
relation.isAuthorOfPublication2545e0fb-d644-4012-8a8a-64144f4cb76b
relation.isAuthorOfPublication.latestForDiscovery2545e0fb-d644-4012-8a8a-64144f4cb76b

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