Evidence map›Paper›PMID 28553950›Full record

ArticleNature immunology2017

Atypical chemokine receptor 1 on nucleated erythroid cells regulates hematopoiesis.

Johan Duchene, Igor Novitzky-Basso, Aude Thiriot, Maria Casanova-Acebes, Mariaelvy Bianchini, S Leah Etheridge, Elin Hub, Katrin Nitz, Katharina Artinger, Kathrin Eller and 8 more

Open access · greenAbstract read
In one paragraph

Article in Nature immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 1 pooled it
9.5field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

58 citing papers in PubMed, 1 synthesis or guideline pooled it, 109 citations in OpenAlex.

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  18. Atypical chemokine receptors in the immune system.Nature reviews. Immunology · 2024
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 10 institutions in 6 countries.

Johan DucheneInstitute for Cardiovascular Prevention, Ludwig-Maximilians University (LMU), Munich, Germany.
Igor Novitzky-BassoBlood and Marrow Transplant Unit, Queen Elizabeth University Hospital, Glasgow, UK.
Aude ThiriotDepartment of Microbiology and Immunobiology and Center for Immune Imaging, Harvard Medical School, Boston, Massachusetts, USA.
Maria Casanova-AcebesFundación Centro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), Madrid, Spain.
Mariaelvy BianchiniInstitute for Cardiovascular Prevention, Ludwig-Maximilians University (LMU), Munich, Germany.
S Leah EtheridgeCentre for Immunology and Infection, Department of Biology, University of York, Heslington, UK.
Elin HubCentre for Immunology and Infection, Department of Biology, University of York, Heslington, UK.
Katrin NitzInstitute for Cardiovascular Prevention, Ludwig-Maximilians University (LMU), Munich, Germany.
Katharina ArtingerCentre for Immunology and Infection, Department of Biology, University of York, Heslington, UK.
Kathrin EllerClinical Division of Nephrology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Jorge CaamañoInstitute of Immunology and Immunotherapy, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.ORCID http://orcid.org/0000-0003-3530-7056
Thomas RülickeInstitute of Laboratory Animal Science, University of Veterinary Medicine Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0002-2121-9496
Paul MossInstitute of Immunology and Immunotherapy, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
Remco T A MegensInstitute for Cardiovascular Prevention, Ludwig-Maximilians University (LMU), Munich, Germany.
Ulrich H von AndrianDepartment of Microbiology and Immunobiology and Center for Immune Imaging, Harvard Medical School, Boston, Massachusetts, USA.
Andres HidalgoInstitute for Cardiovascular Prevention, Ludwig-Maximilians University (LMU), Munich, Germany.ORCID http://orcid.org/0000-0001-5513-555X
Christian WeberInstitute for Cardiovascular Prevention, Ludwig-Maximilians University (LMU), Munich, Germany.
Antal RotInstitute for Cardiovascular Prevention, Ludwig-Maximilians University (LMU), Munich, Germany.
University of York · GBHarvard University · USLudwig-Maximilians-Universität München · DEMaastricht University · NLMedical University of Graz · ATSpanish National Centre for Cardiovascular Research · ESUniversity of Birmingham · GBMax Delbrück Center · DEQueen Elizabeth University Hospital · GBUniversity of Veterinary Medicine Vienna · AT

Funding

Biotechnology and Biological Sciences Research Council BB/K009400/1European Research Council 249929European Research Council 692511Medical Research Council G0802838Wellcome Trust
6 · The paper itself

Abstract

Healthy individuals of African ancestry have neutropenia that has been linked with the variant rs2814778(G) of the gene encoding atypical chemokine receptor 1 (ACKR1). This polymorphism selectively abolishes the expression of ACKR1 in erythroid cells, causing a Duffy-negative phenotype. Here we describe an unexpected fundamental role for ACKR1 in hematopoiesis and provide the mechanism that links its absence with neutropenia. Nucleated erythroid cells had high expression of ACKR1, which facilitated their direct contact with hematopoietic stem cells. The absence of erythroid ACKR1 altered mouse hematopoiesis including stem and progenitor cells, which ultimately gave rise to phenotypically distinct neutrophils that readily left the circulation, causing neutropenia. Individuals with a Duffy-negative phenotype developed a distinct profile of neutrophil effector molecules that closely reflected the one observed in the ACKR1-deficient mice. Thus, alternative physiological patterns of hematopoiesis and bone marrow cell outputs depend on the expression of ACKR1 in the erythroid lineage, findings with major implications for the selection advantages that have resulted in the paramount fixation of the ACKR1 rs2814778(G) polymorphism in Africa.

Indexed as

Duffy Blood-Group SystemErythroblastsHematopoiesisHematopoietic Stem CellsNeutropeniaNeutrophilsReceptors, Cell SurfaceAnimalsBlack PeopleBone MarrowBone Marrow CellsCell ProliferationFlow CytometryFluorescent Antibody TechniqueHumansMiceACKR1 protein, humanAckr1 protein mouseDuffy Blood-Group SystemReceptors, Cell SurfaceReceptors, Chemokine

Identifiers

PMID28553950
PMCPMC5480598
OpenAlexW2620512953

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.