Evidence map›Paper›PMID 32272082›Full record

ArticleImmunity2020

Interleukin-33 Signaling Controls the Development of Iron-Recycling Macrophages.

Yuning Lu, Gemma Basatemur, Ian C Scott, Davide Chiarugi, Marc Clement, James Harrison, Ravin Jugdaohsingh, Xian Yu, Stephen A Newland, Helen E Jolin and 9 more

Open access · hybridAbstract read
In one paragraph

Article in Immunity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 7% 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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

  1. Pooled it
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  13. Molecular and Immunometabolic Landscape of Erythrophagocytosis-induced Ferroptosis.Cardiovascular & hematological disorders drug targets · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 10 institutions in 6 countries.

Yuning LuDivision of Cardiovascular Medicine, University of Cambridge, Cambridge, UK.
Gemma BasatemurDivision of Cardiovascular Medicine, University of Cambridge, Cambridge, UK.
Ian C ScottTranslational Sciences and Experimental Medicine, Early Respiratory and Immunology, Biopharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Davide ChiarugiThe Wellcome-MRC Institute of Metabolic Science-Metabolic Research Laboratories, Cambridge, UK.
Marc ClementDivision of Cardiovascular Medicine, University of Cambridge, Cambridge, UK.
James HarrisonDivision of Cardiovascular Medicine, University of Cambridge, Cambridge, UK.
Ravin JugdaohsinghDepartment of Veterinary Medicine, University of Cambridge, Cambridge, UK.
Xian YuDivision of Cardiovascular Medicine, University of Cambridge, Cambridge, UK.
Stephen A NewlandDivision of Cardiovascular Medicine, University of Cambridge, Cambridge, UK.
Helen E JolinMedical Research Council Laboratory of Molecular Biology, Cambridge, UK.
Xuan LiDivision of Cardiovascular Medicine, University of Cambridge, Cambridge, UK.
Xiao ChenDivision of Cardiovascular Medicine, University of Cambridge, Cambridge, UK; Department of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, China.
Monika SzymanskaDepartment of Pathology, Oslo University Hospital Rikshospitalet, Norway.
Guttorm HaraldsenDepartment of Pathology, Oslo University Hospital Rikshospitalet, Norway.
Gaby PalmerDivision of Rheumatology, Department of Internal Medicine Specialties, University Hospitals of Geneva, Geneva, Switzerland; Department of Pathology-Immunology, University of Geneva School of Medicine, Geneva, Switzerland.
Padraic G FallonSchool of Medicine, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin 2, Ireland.
E Suzanne CohenBioscience Asthma, Early Respiratory and Immunology, BioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Andrew N J McKenzieMedical Research Council Laboratory of Molecular Biology, Cambridge, UK.
Ziad MallatDivision of Cardiovascular Medicine, University of Cambridge, Cambridge, UK; Institut National de la Santé et de la Recherche Médicale, Paris Cardiovascular Research Center, Paris, France. Electronic address: zm255@medschl.cam.ac.uk.
University of Cambridge · GBAstraZeneca (United Kingdom) · GBOslo University Hospital · NOHuazhong University of Science and Technology · CNInserm · FRMedical Research Council · GBMRC Laboratory of Molecular Biology · GBTrinity College Dublin · IEUniversity Hospital of Geneva · CHWellcome/MRC Institute of Metabolic Science · GB

Funding

British Heart Foundation CH/10/001/27642British Heart Foundation PG/17/9/32834British Heart Foundation RG/15/11/31593Medical Research Council MC_U105178805Medical Research Council MR/R005699/1Wellcome Trust
6 · The paper itself

Abstract

Splenic red pulp macrophages (RPMs) contribute to erythrocyte homeostasis and are required for iron recycling. Heme induces the expression of SPIC transcription factor in monocyte-derived macrophages and promotes their differentiation into RPM precursors, pre-RPMs. However, the requirements for differentiation into mature RPMs remain unknown. Here, we have demonstrated that interleukin (IL)-33 associated with erythrocytes and co-cooperated with heme to promote the generation of mature RPMs through activation of the MyD88 adaptor protein and ERK1/2 kinases downstream of the IL-33 receptor, IL1RL1. IL-33- and IL1RL1-deficient mice showed defective iron recycling and increased splenic iron deposition. Gene expression and chromatin accessibility studies revealed a role for GATA transcription factors downstream of IL-33 signaling during the development of pre-RPMs that retained full potential to differentiate into RPMs. Thus, IL-33 instructs the development of RPMs as a response to physiological erythrocyte damage with important implications to iron recycling and iron homeostasis.

Indexed as

AnimalsErythrocytesHemeHomeostasisInterleukin-1 Receptor-Like 1 ProteinInterleukin-33IronMacrophagesMice, KnockoutMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Myeloid Differentiation Factor 88Signal TransductionSpleenHemeInterleukin-1 Receptor-Like 1 ProteinInterleukin-33IronMapk1 protein, mouseMapk3 protein, mouseMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Myd88 protein, mouseMyeloid Differentiation Factor 88erythrophagocytosisinterleukin-33interleukin-33 receptorinterleukinsiron metabolismred pulp macrophage

Identifiers

PMID32272082
PMCPMC7237885
OpenAlexW3016195946

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.