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dc.contributor.authorSchraml, BU
dc.contributor.authorvan Blijswijk, J
dc.contributor.authorZelenay, S
dc.contributor.authorWhitney, PG
dc.contributor.authorFilby, A
dc.contributor.authorActon, SE
dc.contributor.authorRogers, NC
dc.contributor.authorMoncaut, N
dc.contributor.authorCarvajal, JJ
dc.contributor.authorReis e Sousa, C
dc.date.accessioned2018-08-06T09:46:59Z
dc.date.issued2013-08-15
dc.identifier4
dc.identifier.citationCELL, 2013, 154 pp. 843 - 858
dc.identifier.issn0092-8674
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/2268
dc.identifier.doi10.1016/j.cell.2013.07.014
dc.description.abstractMononuclear phagocytes are classified as macrophages or dendritic cells (DCs) based on cell morphology, phenotype, or select functional properties. However, these attributes are not absolute and often overlap, leading to difficulties in cell-type identification. To circumvent this issue, we describe a mouse model to define DCs based on their ontogenetic descendence from a committed precursor. We show that precursors of mouse conventional DCs, but not other leukocytes, are marked by expression of DNGR-1. Genetic tracing of DNGR-1 expression history specifically marks cells traditionally ascribed to the DC lineage, and this restriction is maintained after inflammation. Notably, in some tissues, cells previously thought to be monocytes/macrophages are in fact descendants from DC precursors. These studies provide an in vivo model for fate mapping of DCs, distinguishing them from other leukocyte lineages, and thus help to unravel the functional complexity of the mononuclear phagocyte system.
dc.format.extent843 - 858
dc.languageeng
dc.language.isoeng
dc.publisherCELL PRESS
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.titleGenetic Tracing via DNGR-1 Expression History Defines Dendritic Cells as a Hematopoietic Lineage
dc.typeJournal Article
rioxxterms.versionofrecord10.1016/j.cell.2013.07.014
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2013-08-15
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfCELL
pubs.notesaffiliation: Sousa, CRE (Reprint Author), Canc Res UK London Res Inst, Lincolns Inn Fields Labs, Immunobiol Lab, 44 Lincolns Inn Fields, London WC2A 3LY, England. Schraml, Barbara U.; van Blijswijk, Janneke; Zelenay, Santiago; Whitney, Paul G.; Acton, Sophie E.; Rogers, Neil C.; Reis e Sousa, Caetano, Canc Res UK London Res Inst, Lincolns Inn Fields Labs, Immunobiol Lab, London WC2A 3LY, England. Filby, Andrew, Canc Res UK London Res Inst, Lincolns Inn Fields Labs, Flow Cytometry Lab, London WC2A 3LY, England. Acton, Sophie E., UCL, Dept Cell & Dev Biol, London WC1E 6BT, England. Moncaut, Natalia; Carvajal, Jaime J., Inst Canc Res, Chester Beatty Labs, Div Canc Biol, London SW3 6JB, England. Carvajal, Jaime J., CSIC UPO JA, Ctr Andaluz Biol Desarrollo, Seville 41013, Spain. keywords-plus: TRANSCRIPTION FACTOR ZDC; C-TYPE LECTIN; STEADY-STATE; IN-VIVO; TISSUE MACROPHAGES; BONE-MARROW; STEM-CELLS; MONOCYTES; PROGENITORS; HOMEOSTASIS research-areas: Biochemistry & Molecular Biology; Cell Biology web-of-science-categories: Biochemistry & Molecular Biology; Cell Biology author-email: [email protected] researcherid-numbers: Carvajal, Jaime/O-3681-2014 Acton, Sophie/G-9784-2012 orcid-numbers: Carvajal, Jaime/0000-0002-7277-0317 Acton, Sophie/0000-0003-2704-716X Whitney, Paul/0000-0003-3836-7601 Reis e Sousa, Caetano/0000-0001-7392-2119 Zelenay, Santiago/0000-0002-6865-3978 funding-acknowledgement: Cancer Research UK; European Research Council (ERC) [AdG-2010-268670]; EMBO long-term fellowship; Boehringer Ingelheim Fonds; Overseas Biomedical Fellowship from the NHMRC of Australia; Henry Wellcome Fellowship [WT089009MA]; Cancer Research UK [15689] funding-text: We thank Frederic Geissmann and members of the Immunobiology Laboratory for helpful discussions and suggestions. C. R. S. is funded by Cancer Research UK, a prize from Fondation Bettencourt-Schueller, and a grant from the European Research Council (ERC Advanced Researcher Grant AdG-2010-268670). B. U. S. was supported by an EMBO long-term fellowship, J.v.B. was supported by Boehringer Ingelheim Fonds, P. G. W. was supported by an Overseas Biomedical Fellowship from the NHMRC of Australia, and S. E. A. was supported by a Henry Wellcome Fellowship (WT089009MA). We thank CRUK Transgenic Services for generation of genetically modified mice and the Biological Resources staff for animal care and assistance with mouse experiments. We thank Yasmine Belkaid and John Grainger for their help with the isolation of intestinal lamina propria cells. number-of-cited-references: 52 times-cited: 120 usage-count-last-180-days: 0 usage-count-since-2013: 18 journal-iso: Cell doc-delivery-number: 202GQ unique-id: ISI:000323202500015 oa: gold_or_bronze da: 2018-08-06
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR
pubs.volume154en_US
pubs.embargo.termsNot known
dc.contributor.icrauthorMoncaut, Nataliaen


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