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dc.contributor.authorM. Bellette, Bernadetteen_US
dc.contributor.authorM. Woods, Gregoryen_US
dc.contributor.authorWozniak, Teresaen_US
dc.contributor.authorV. Doherty, Kathleenen_US
dc.contributor.authorKonrad Muller, H.en_US
dc.date.accessioned2017-05-03T14:39:50Z
dc.date.available2017-05-03T14:39:50Z
dc.date.issued2003en_US
dc.date.modified2010-01-13T06:51:48Z
dc.identifier.issn00192805en_US
dc.identifier.doi10.1111/j.1365-2567.2003.01759.xen_AU
dc.identifier.urihttp://hdl.handle.net/10072/28266
dc.description.abstractAntigen treatment of neonatal epidermis results in antigen-specific immune suppression. Compared with adult counterparts, neonatal Langerhans' cells (LC) demonstrate an impaired ability to transport antigen to the lymph node (LN). As it is possible that neonatal LC have a reduced ability to endocytose antigen, we evaluated the acquisition of endocytic function, the expression of uptake receptors and the internalization of soluble and small particulate antigens in neonatal, juvenile and adult mice. Although LC from 4-day-old mice were weakly positive for the mannose-type receptor, Langerin, they were capable of internalizing fluorescein isothiocyanate (FITC)-dextran, but to a lesser extent than LC from 6-week-old mice. However, when ratio data were calculated to account for variations in fluorescence intensity at 4ଠit was demonstrated that neonatal LC continued to internalize antigen over a longer period of time than adult mice and, as the ratios were much higher, that neonatal cells were also relatively more efficient in antigen uptake. When receptors for mannan and mannose were competitively blocked, LC from neonatal mice, but not adult mice, could still efficiently internalize FITC-dextran. Consequently, the uptake of FITC-dextran, in part, occurred via alternative receptors or a receptor-independent fluid-phase pathway. A feasible pathway is macropinocytosis, as LC from 4-day-old mice demonstrated a reduction in FITC-dextran internalization by the macropinocytosis inhibitor, wortmannin. Evidence of a functional macropinocytosis pathway in neonatal LC was further supported by internalization of the soluble tracer Lucifer Yellow (LY). We conclude that neonatal LC preferentially utilize a wortmannin-sensitive, fluid-phase pathway, rather than receptor-mediated endocytosis, to internalize antigen. As neonatal LC are capable of sampling their environment without inducing immunity, this may serve to avoid inappropriate immune responses during the neonatal period.en_US
dc.description.peerreviewedYesen_US
dc.description.publicationstatusYesen_AU
dc.languageEnglishen_US
dc.language.isoen_AU
dc.publisherBlackwell Synergyen_US
dc.publisher.placeUKen_US
dc.relation.ispartofpagefrom466en_US
dc.relation.ispartofpageto473en_US
dc.relation.ispartofissue4en_US
dc.relation.ispartofjournalImmunologyen_US
dc.relation.ispartofvolume110en_US
dc.subject.fieldofresearchcode320202en_US
dc.titleDEC-205lo Langerinlo neonatal Langerhans' cells preferentially utilize a wortmannin-sensitive, fluid-phase pathway to internalize exogenous antigenen_US
dc.typeJournal articleen_US
dc.type.descriptionC1 - Peer Reviewed (HERDC)en_US
dc.type.codeC - Journal Articlesen_US
gro.date.issued2003
gro.hasfulltextNo Full Text
gro.griffith.authorBellette, Bernadette


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