Bovine peripheral blood MSCs chemotax towards inflammation and embryo implantation stimuli

dc.contributor.authorCalle, Alexandra
dc.contributor.authorGutiérrez-Reinoso, Miguel Ángel
dc.contributor.authorRe, Michela Tatiana
dc.contributor.authorBlanco Murcia, Francisco Javier
dc.contributor.authorde la Fuente, Julio
dc.contributor.authorMonguió-Tortajada, Marta
dc.contributor.authorEnric Borràs, Francesc
dc.contributor.authorYáñez-Mó, María
dc.contributor.authorRamírez, Miguel Ángel
dc.date.accessioned2025-01-28T14:26:48Z
dc.date.available2025-01-28T14:26:48Z
dc.date.issued2020
dc.description.abstractMesenchymal stem cells (MSCs) have a great potential in regenerative medicine because of their multipotential and immunoregulatory capacities, while in early pregnancy they could participate in the immunotolerance of the mother towards the embryo. Peripheral blood constitutes an accessible source of MSCs. We successfully isolated peripheral blood MSC (pbMSCs) lines, with or without previous bone marrow mobilization. All pbMSCs lines obtained in both conditions presented classical MSC markers and properties, alkaline phosphatase activity and multipotent capacity to differentiate among adipogenic, osteogenic or chondrogenic lineages, and suppressed the proliferation of T cells. pbMSCs showed migratory capacity without cytokine stimulation while increasing their migration rate in the presence of inflammatory or embryo implantation stimuli. Interestingly, in contrast to MSCs derived from endometrial tissue, three pbMSCs lines also showed increased migration towards the IFN‐τ implantation cytokine. Moreover, the secretome produced by an early implantation stage embryonic trophectoderm cell line showed a chemoattractant effect in pbMSCs. Our results suggest that circulating MSCs are present in the peripheral blood under healthy conditions. The fact that both the inflammation and implantation signals induced pbMSCs chemotaxis highlights MSC heterogeneity and suggests that their migratory capacity may differ according to their tissue of origin and would suggest the possible active recruitment of MSCs from bone marrow during pregnancy to repress the immune response to prevent the embryo rejection by the maternal organism.
dc.description.departmentDepto. de Medicina y Cirugía Animal
dc.description.facultyFac. de Veterinaria
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Industria y Competitividad (España)
dc.description.sponsorshipMinisterio de Ciencia e Innovación (España)
dc.description.sponsorshipMinisterio de Transición Ecológica (España)
dc.description.sponsorshipFundación Biodiversidad
dc.description.statuspub
dc.identifier.citationCalle, Alexandra, et al. «Bovine Peripheral Blood MSCs Chemotax towards Inflammation and Embryo Implantation Stimuli». Journal of Cellular Physiology, vol. 236, n.o 2, febrero de 2021, pp. 1054-67. https://doi.org/10.1002/jcp.29915.
dc.identifier.doi10.1002/jcp.29915
dc.identifier.officialurlhttps://doi.org/10.1002/jcp.29915
dc.identifier.urihttps://hdl.handle.net/20.500.14352/116630
dc.issue.number2
dc.journal.titleJournal of Cellular Physiology
dc.language.isoeng
dc.page.final1067
dc.page.initial1054
dc.publisherWiley
dc.relation.projectIDPID2019‐107145RB‐I00
dc.relation.projectID731014
dc.relation.projectIDPRCV00820
dc.relation.projectIDAGL2015‐70140‐R
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.accessRightsrestricted access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.cdu61
dc.subject.keywordCell migration
dc.subject.keywordEmbryo implantation
dc.subject.keywordGranulocyte colony‐stimulating factor
dc.subject.keywordImmunoregulation
dc.subject.keywordPeripheral blood mesenchymal stem cells
dc.subject.ucmCiencias Biomédicas
dc.subject.unesco32 Ciencias Médicas
dc.titleBovine peripheral blood MSCs chemotax towards inflammation and embryo implantation stimuli
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number236
dspace.entity.typePublication
relation.isAuthorOfPublication21609857-9d85-404c-a367-476ca0575d0a
relation.isAuthorOfPublication345fa1ec-7a50-42f6-aa54-264929c135c5
relation.isAuthorOfPublication.latestForDiscovery21609857-9d85-404c-a367-476ca0575d0a

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