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dc.contributor.authorFurmanski, Anna L.en
dc.contributor.authorSaldana, Jose Ignacioen
dc.contributor.authorRowbotham, Nicola J.en
dc.contributor.authorRoss, Susanen
dc.contributor.authorCrompton, Tessaen
dc.date.accessioned2019-08-22T15:16:52Z
dc.date.available2019-08-22T15:16:52Z
dc.date.issued2011-11-21
dc.identifier.citationFurmanski AL, Saldana JI, Rowbotham NJ, Ross SE, Crompton T (2012) 'Role of Hedgehog signalling at the transition from double-positive to single-positive thymocyte', European Journal of Immunology, 42 (2), pp.489-499.en
dc.identifier.issn0014-2980
dc.identifier.pmid22101858
dc.identifier.doi10.1002/eji.201141758
dc.identifier.urihttp://hdl.handle.net/10547/623394
dc.description.abstractIn the thymus, developing T cells receive signals that determine lineage choice, specificity, MHC restriction and tolerance to self‐antigen. One way in which thymocytes receive instruction is by secretion of Sonic hedgehog (Shh) from thymic epithelial cells. We have previously shown that Hedgehog (Hh) signalling in the thymus decreases the CD4:CD8 single‐positive (SP) thymocyte ratio. Here, we present data indicating that double‐positive (DP) thymocytes are Hh‐responsive and that thymocyte‐intrinsic Hh signalling plays a role in modulating the production of CD4+ (SP4), CD8+ (SP8) and unconventional T‐cell subsets. Repression of physiological Hh signalling in thymocytes altered the proportions of DP and SP4 cells. Thymocyte‐intrinsic Hh‐dependent transcription also attenuated both the production of mature SP4 and SP8 cells, and the establishment of peripheral T‐cell compartments in TCR‐transgenic mice. Additionally, stimulation or withdrawal of Hh signals in the WT foetal thymus impaired or enhanced upregulation of the CD4 lineage‐specific transcription factor Gata3 respectively. These data together suggest that Hh signalling may play a role in influencing the later stages of thymocyte development.
dc.language.isoenen
dc.publisherWileyen
dc.relation.urlhttps://onlinelibrary.wiley.com/doi/full/10.1002/eji.201141758en
dc.rightsYellow - can archive pre-print (ie pre-refereeing)
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectHedgehog (Hh)en
dc.subjectC550 Immunologyen
dc.titleRole of Hedgehog signalling at the transition from double-positive to single-positive thymocyteen
dc.typeArticleen
dc.identifier.journalEuropean Journal of Immunologyen
dc.identifier.pmcidPMC3378705
dc.date.updated2019-08-22T15:07:09Z
html.description.abstractIn the thymus, developing T cells receive signals that determine lineage choice, specificity, MHC restriction and tolerance to self‐antigen. One way in which thymocytes receive instruction is by secretion of Sonic hedgehog (Shh) from thymic epithelial cells. We have previously shown that Hedgehog (Hh) signalling in the thymus decreases the CD4:CD8 single‐positive (SP) thymocyte ratio. Here, we present data indicating that double‐positive (DP) thymocytes are Hh‐responsive and that thymocyte‐intrinsic Hh signalling plays a role in modulating the production of CD4+ (SP4), CD8+ (SP8) and unconventional T‐cell subsets. Repression of physiological Hh signalling in thymocytes altered the proportions of DP and SP4 cells. Thymocyte‐intrinsic Hh‐dependent transcription also attenuated both the production of mature SP4 and SP8 cells, and the establishment of peripheral T‐cell compartments in TCR‐transgenic mice. Additionally, stimulation or withdrawal of Hh signals in the WT foetal thymus impaired or enhanced upregulation of the CD4 lineage‐specific transcription factor Gata3 respectively. These data together suggest that Hh signalling may play a role in influencing the later stages of thymocyte development.


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