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IL-7 sustains CD31 expression in human naive CD4+ T cells and preferentially expands the CD31+ subset in a PI3K-dependent manner

dc.contributor.authorAzevedo, R. I.
dc.contributor.authorSoares, M. V.
dc.contributor.authorBarata, J. T.
dc.contributor.authorTendeiro, R.
dc.contributor.authorSerra-Caetano, A.
dc.contributor.authorVictorino, R. M.
dc.contributor.authorSousa, A. E.
dc.date.accessioned2015-02-03T16:02:11Z
dc.date.available2015-02-03T16:02:11Z
dc.date.issued2008
dc.description© 2009 by The American Society of Hematologypor
dc.description.abstractThe CD31(+) subset of human naive CD4(+) T cells is thought to contain the population of cells that have recently emigrated from the thymus, while their CD31(-) counterparts have been proposed to originate from CD31(+) cells after homeostatic cell division. Naive T-cell maintenance is known to involve homeostatic cytokines such as interleukin-7 (IL-7). It remains to be investigated what role this cytokine has in the homeostasis of naive CD4(+) T-cell subsets defined by CD31 expression. We provide evidence that IL-7 exerts a preferential proliferative effect on CD31(+) naive CD4(+) T cells from adult peripheral blood compared with the CD31(-) subset. IL-7-driven proliferation did not result in loss of CD31 expression, suggesting that CD31(+) naive CD4(+) T cells can undergo cytokine-driven homeostatic proliferation while preserving CD31. Furthermore, IL-7 sustained or increased CD31 expression even in nonproliferating cells. Both proliferation and CD31 maintenance were dependent on the activation of phosphoinositide 3-kinase (PI3K) signaling. Taken together, our data suggest that during adulthood CD31(+) naive CD4(+) T cells are maintained by IL-7 and that IL-7-based therapies may exert a preferential effect on this population.por
dc.description.sponsorshipThis work was supported by grant POCI/BIA-BCM/61079/2004 from Fundação para a Ciência e a Tecnologia (FCT) and by Programa Operacional Ciência e Inovação 2010 (POCI2010; to M.V.D.S.) R.I.A., M.V.D.S., and R.T. received scholarships from FCT cofinanced by POCI 2010 and FSE.por
dc.identifier.citationBlood, 26 March 2009, Volume 113, Number 13por
dc.identifier.issn0006-4971
dc.identifier.urihttp://dx.doi.org/10.1182/blood-2008-07-166223
dc.identifier.urihttp://hdl.handle.net/10451/15874
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherAmerican Society of Hematologypor
dc.relation.publisherversionThe definitive version is available at http://www.bloodjournal.org/por
dc.titleIL-7 sustains CD31 expression in human naive CD4+ T cells and preferentially expands the CD31+ subset in a PI3K-dependent mannerpor
dc.typejournal article
dspace.entity.typePublication
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/POCI/POCI%2FBIA-BCM%2F61079%2F2004/PT
oaire.citation.titleBloodpor
oaire.fundingStreamPOCI
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsclosedAccesspor
rcaap.typearticlepor
relation.isProjectOfPublication97013015-4d59-4ff6-b9ba-2d1b16ce7242
relation.isProjectOfPublication.latestForDiscovery97013015-4d59-4ff6-b9ba-2d1b16ce7242

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