Evidence map›Paper›PMID 26642357›Full record

ArticleNature immunology2016

Self-renewing resident arterial macrophages arise from embryonic CX3CR1(+) precursors and circulating monocytes immediately after birth.

Sherine Ensan, Angela Li, Rickvinder Besla, Norbert Degousee, Jake Cosme, Mark Roufaiel, Eric A Shikatani, Mahmoud El-Maklizi, Jesse W Williams, Lauren Robins and 24 more

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In one paragraph

Article in Nature immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 221 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
221citing papers in PubMed, 2 pooled it
14.4field-weighted citation impact, top 1% 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

221 citing papers in PubMed, 2 syntheses or guidelines pooled it, 357 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
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  9. NFAT1Cellular & molecular biology letters · 2026
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  19. Macrophage Mayhem in Aortic Aneurysm.JACC. Basic to translational science · 2025
    Article
  20. Article

161 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

34 authors at 8 institutions in 3 countries.

Sherine EnsanDepartment of Immunology, University of Toronto, Toronto, Ontario, Canada.
Angela LiDepartment of Immunology, University of Toronto, Toronto, Ontario, Canada.
Rickvinder BeslaDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
Norbert DegouseeToronto General Research Institute, University Health Network, Toronto, Ontario, Canada.
Jake CosmeToronto General Research Institute, University Health Network, Toronto, Ontario, Canada.
Mark RoufaielToronto General Research Institute, University Health Network, Toronto, Ontario, Canada.ORCID http://orcid.org/0000-0003-4174-1043
Eric A ShikataniDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
Mahmoud El-MakliziDepartment of Immunology, University of Toronto, Toronto, Ontario, Canada.
Jesse W WilliamsDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Lauren RobinsToronto General Research Institute, University Health Network, Toronto, Ontario, Canada.
Cedric LiToronto General Research Institute, University Health Network, Toronto, Ontario, Canada.
Bonnie LewisToronto General Research Institute, University Health Network, Toronto, Ontario, Canada.
Tae Jin YunLaboratory of Cellular Physiology and Immunology, Institut de Recherches Cliniques de Montréal, Montréal, Quebec, Canada.
Jun Seong LeeLaboratory of Cellular Physiology and Immunology, Institut de Recherches Cliniques de Montréal, Montréal, Quebec, Canada.
Peter WieghoferInstitute of Neuropathology and Faculty of Biology, University of Freiburg, Freiburg, Germany.
Ramzi KhattarToronto General Research Institute, University Health Network, Toronto, Ontario, Canada.
Kaveh FarrokhiDepartment of Immunology, University of Toronto, Toronto, Ontario, Canada.
John ByrneToronto General Research Institute, University Health Network, Toronto, Ontario, Canada.
Maral OuzounianToronto General Research Institute, University Health Network, Toronto, Ontario, Canada.
Caleb C J ZavitzToronto General Research Institute, University Health Network, Toronto, Ontario, Canada.
Gary A LevyDepartment of Immunology, University of Toronto, Toronto, Ontario, Canada.
Carla M T BauerHoffmann-La Roche, pRED, Pharma Research and Early Development, DTA Inflammation, Nutley, New Jersey, USA.
Peter LibbyDepartment of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Mansoor HusainDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
Filip K SwirskiCenter for Systems Biology, Massachusetts General Hospital, Harvard Medical School, Boston,MA, USA.
Cheolho CheongLaboratory of Cellular Physiology and Immunology, Institut de Recherches Cliniques de Montréal, Montréal, Quebec, Canada.
Marco PrinzInstitute of Neuropathology and BIOSS Centre for Biological Signaling Studies, University of Freiburg, Freiburg, Germany.
Ingo HilgendorfDepartment of Cardiology and Angiology I, Heart Center, University of Freiburg, Freiburg, Germany.
Gwendalyn J RandolphDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Slava EpelmanDepartment of Immunology, University of Toronto, Toronto, Ontario, Canada.
Anthony O GramoliniToronto General Research Institute, University Health Network, Toronto, Ontario, Canada.
Myron I CybulskyDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
Barry B RubinToronto General Research Institute, University Health Network, Toronto, Ontario, Canada.
Clinton S RobbinsDepartment of Immunology, University of Toronto, Toronto, Ontario, Canada.
University Health Network · CAUniversity of Toronto · CAMontreal Clinical Research Institute · CAUniversity of Freiburg · DEWashington University in St. Louis · USBrigham and Women's Hospital · USHarvard University · USLa Roche College · US

Funding

Differentiation/migratory fate of monocyte-derived cellsR01AI049653 · NIAID · WASHINGTON UNIVERSITY · PI Gwendalyn J Randolph · 2000 to 2026
$4.6M
CIHR MOP133390NIAID NIH HHS R01 AI049653
6 · The paper itself

Abstract

Resident macrophages densely populate the normal arterial wall, yet their origins and the mechanisms that sustain them are poorly understood. Here we use gene-expression profiling to show that arterial macrophages constitute a distinct population among macrophages. Using multiple fate-mapping approaches, we show that arterial macrophages arise embryonically from CX3CR1(+) precursors and postnatally from bone marrow-derived monocytes that colonize the tissue immediately after birth. In adulthood, proliferation (rather than monocyte recruitment) sustains arterial macrophages in the steady state and after severe depletion following sepsis. After infection, arterial macrophages return rapidly to functional homeostasis. Finally, survival of resident arterial macrophages depends on a CX3CR1-CX3CL1 axis within the vascular niche.

Indexed as

Cell Self RenewalAnimalsCell SurvivalChemokine CX3CL1Cluster AnalysisCX3C Chemokine Receptor 1Embryonic Stem CellsFemaleGene Expression ProfilingImmunophenotypingMacrophagesMaleMiceMice, TransgenicMonocytesPhenotypeChemokine CX3CL1CX3C Chemokine Receptor 1Cx3cr1 protein, mouseReceptors, Chemokine

Identifiers

PMID26642357
OpenAlexW2242760558

What OpenQuestion holds

Textmetadata
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.