Publication:
Rhythmic modulation of the hematopoietic niche through neutrophil clearance.

dc.contributor.authorCasanova-Acebes, Maria
dc.contributor.authorPitaval, Christophe
dc.contributor.authorWeiss, Linnea A
dc.contributor.authorNombela-Arrieta, César
dc.contributor.authorChèvre, Raphaël
dc.contributor.authorA-González, Noelia
dc.contributor.authorKunisaki, Yuya
dc.contributor.authorZhang, Dachuan
dc.contributor.authorvan Rooijen, Nico
dc.contributor.authorSilberstein, Leslie E
dc.contributor.authorWeber, Christian
dc.contributor.authorNagasawa, Takashi
dc.contributor.authorFrenette, Paul S
dc.contributor.authorCastrillo, Antonio
dc.contributor.authorHidalgo, Andrés
dc.date.accessioned2026-02-22T16:28:24Z
dc.date.available2026-02-22T16:28:24Z
dc.date.issued2013-05-23
dc.descriptionWe thank M. Nacher, J. Ogonek, I. Ortega, V. Zorita, M. Leboeuf, J.M. Ligos, and the Cellomics, Microscopy, and Comparative Medicine Units at CNIC for technical support; J. Garaude, D. Lucas, and A. Ramiro for critically reviewing the manuscript; and S. Gonzalez and D. Sanz for reagents. This study was supported by Deutsche Forschungsgemeinschaft (DFG WE1913/11-2 and SFB914-B8) to C.W.; R01-DK056638 and R01-HL69438 to P.S.F.; grants SAF2008-00057 and SAF2011-29244 to A.C.; Ramon y Cajal Fellowship (RYC-2007-00697) and SAF2009-11037 from MINECO, S2010/BMD-2314 from Comunidad de Madrid, and FP7-People-IRG Program (246655) to A.H.; C.N-A. is funded by a Human Frontiers in Science Program long-term fellowship 00194/2008. M.C-A. is supported by a FPI fellowship from the Spanish Ministry of Economy and Competitivity. The Centro Nacional de Investigaciones Cardiovasculares is supported by the Spanish Ministry of Economy and Competitivity and the Pro-CNIC Foundation. M.C-A performed experiments and wrote the manuscript; L.A.W., C.P., and N.A-G performed experiments and edited the manuscript. C.N-A., R.C., Y.K., and D.Z. performed experiments; N.V.R., L.E.S., C.W., T.N., P.S.F., and A.C. contributed reagents, discussed experiments and helped in editing the manuscript; A.H. conceived the study, performed experiments and wrote the manuscript. C.P., L.A.W., and C.N-A. contributed equally to this study.
dc.description.abstractUnique among leukocytes, neutrophils follow daily cycles of release from and migration back into the bone marrow, where they are eliminated. Because removal of dying cells generates homeostatic signals, we explored whether neutrophil elimination triggers circadian events in the steady state. Here, we report that the homeostatic clearance of neutrophils provides cues that modulate the physiology of the bone marrow. We identify a population of CD62L(LO) CXCR4(HI) neutrophils that have "aged" in the circulation and are eliminated at the end of the resting period in mice. Aged neutrophils infiltrate the bone marrow and promote reductions in the size and function of the hematopoietic niche. Modulation of the niche depends on macrophages and activation of cholesterol-sensing nuclear receptors and is essential for the rhythmic egress of hematopoietic progenitors into the circulation. Our results unveil a process that synchronizes immune and hematopoietic rhythms and expand the ascribed functions of neutrophils beyond inflammation. PAPERFLICK:
dc.description.peerreviewed
dc.format.number5
dc.format.page1025-1035
dc.format.volume153
dc.identifier.citationCell . 2013 May 23;153(5):1025-35.
dc.identifier.journalCell
dc.identifier.pubmedID23706740
dc.identifier.urihttps://hdl.handle.net/20.500.12105/27256
dc.language.isoeng
dc.publisherCell Press
dc.relation.publisherversionhttp://doi: 10.1016/j.cell.2013.04.040.
dc.repisalud.institucionCNIO
dc.rights.accessRightsopen access
dc.rights.licenseAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectSTEM-CELL NICHE
dc.subjectBONE MARROW
dc.subjectG-CSF
dc.subjectPROGENITOR CELLS
dc.subjectP-SELECTIN
dc.subjectINFLAMMATION
dc.subjectCXCR4
dc.subjectMOBILIZATION
dc.subjectRELEASE
dc.subjectMICE
dc.titleRhythmic modulation of the hematopoietic niche through neutrophil clearance.
dc.typeresearch article
dc.type.hasVersionVoR
dspace.entity.typePublication
relation.isAuthorOfPublication047b3088-9438-489e-9e86-15da17e2f4da
relation.isAuthorOfPublication.latestForDiscovery047b3088-9438-489e-9e86-15da17e2f4da

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