Evidence map›Paper›PMID 33875597›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2021

GPR182 is an endothelium-specific atypical chemokine receptor that maintains hematopoietic stem cell homeostasis.

Alan Le Mercier, Remy Bonnavion, Weijia Yu, Mohamad Wessam Alnouri, Sophie Ramas, Yang Zhang, Yannick Jäger, Kenneth Anthony Roquid, Hyun-Woo Jeong, Kishor Kumar Sivaraj and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.0field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 45 citations in OpenAlex.

  1. Mechanisms of XCR1 Membrane Trafficking and Constitutive Endocytosis.Basic & clinical pharmacology & toxicology · 2026
    Article
  2. Review
  3. Review
  4. GPR182 and the reframing of lacteal chylomicron uptake.The Journal of clinical investigation · 2026
    Article
  5. GPR182 is a lipoprotein receptor for dietary fat absorption.The Journal of clinical investigation · 2026
    Article
  6. Review
  7. Atypical GPCR Activation Resolved by Nanobody Engineering.bioRxiv : the preprint server for biology · 2026
    Article
  8. Article
  9. In silico pharmacology · 2026
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Exploring G Protein-Coupled Receptors in Hematological Cancers.ACS pharmacology & translational science · 2024
    Article
  15. Review
  16. Atypical chemokine receptors in the immune system.Nature reviews. Immunology · 2024
    Review
  17. Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 4 institutions in 2 countries.

Alan Le MercierDepartment of Pharmacology, Max Planck Institute for Heart and Lung Research, Bad Nauheim, 61231, Germany.
Remy BonnavionDepartment of Pharmacology, Max Planck Institute for Heart and Lung Research, Bad Nauheim, 61231, Germany; remy.bonnavion@mpi-bn.mpg.de Stefan.Offermanns@mpi-bn.mpg.de.ORCID 0000-0002-7389-4282
Weijia YuDepartment of Medicine, Hematology/Oncology, Goethe University Hospital, 60590 Frankfurt, Germany.
Mohamad Wessam AlnouriDepartment of Pharmacology, Max Planck Institute for Heart and Lung Research, Bad Nauheim, 61231, Germany.
Sophie RamasDepartment of Pharmacology, Max Planck Institute for Heart and Lung Research, Bad Nauheim, 61231, Germany.ORCID 0000-0002-7186-264X
Yang ZhangDepartment of Biosystems Science and Engineering, Eidgenössische Technische Hochschule (ETH) Zurich, 4058 Basel, Switzerland.ORCID 0000-0002-1763-6908
Yannick JägerDepartment of Pharmacology, Max Planck Institute for Heart and Lung Research, Bad Nauheim, 61231, Germany.ORCID 0000-0003-1712-3712
Kenneth Anthony RoquidDepartment of Pharmacology, Max Planck Institute for Heart and Lung Research, Bad Nauheim, 61231, Germany.
Hyun-Woo JeongDepartment of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, 48149 Münster, Germany.ORCID 0000-0002-6976-6739
Kishor Kumar SivarajDepartment of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, 48149 Münster, Germany.ORCID 0000-0002-5321-3400
Haaglim ChoDepartment of Pharmacology, Max Planck Institute for Heart and Lung Research, Bad Nauheim, 61231, Germany.ORCID 0000-0002-6577-5320
Xinyi ChenDepartment of Pharmacology, Max Planck Institute for Heart and Lung Research, Bad Nauheim, 61231, Germany.
Boris StrilicDepartment of Pharmacology, Max Planck Institute for Heart and Lung Research, Bad Nauheim, 61231, Germany.
Tjeerd SijmonsmaDepartment of Medicine, Hematology/Oncology, Goethe University Hospital, 60590 Frankfurt, Germany.ORCID 0000-0001-8950-2987
Ralf AdamsDepartment of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, 48149 Münster, Germany.ORCID 0000-0003-3031-7677
Timm SchroederDepartment of Biosystems Science and Engineering, Eidgenössische Technische Hochschule (ETH) Zurich, 4058 Basel, Switzerland.ORCID 0000-0001-9320-0252
Michael A RiegerDepartment of Medicine, Hematology/Oncology, Goethe University Hospital, 60590 Frankfurt, Germany.ORCID 0000-0002-4158-5872
Stefan OffermannsDepartment of Pharmacology, Max Planck Institute for Heart and Lung Research, Bad Nauheim, 61231, Germany; remy.bonnavion@mpi-bn.mpg.de Stefan.Offermanns@mpi-bn.mpg.de.ORCID 0000-0001-8676-6805
Max Planck Institute for Heart and Lung Research · DEGoethe University Frankfurt · DEMax Planck Institute for Molecular Biomedicine · DEBoard of the Swiss Federal Institutes of Technology · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

G protein-coupled receptor 182 (GPR182) has been shown to be expressed in endothelial cells; however, its ligand and physiological role has remained elusive. We found GPR182 to be expressed in microvascular and lymphatic endothelial cells of most organs and to bind with nanomolar affinity the chemokines CXCL10, CXCL12, and CXCL13. In contrast to conventional chemokine receptors, binding of chemokines to GPR182 did not induce typical downstream signaling processes, including G

Indexed as

Animalsbeta-ArrestinsChemokine CXCL10Chemokine CXCL12Chemokine CXCL13ChemokinesEndothelial CellsFemaleHEK293 CellsHematopoietic Stem CellsHomeostasisHumansMaleMiceMice, Inbred C57BLReceptors, Chemokinebeta-ArrestinsChemokine CXCL10Chemokine CXCL12Chemokine CXCL13ChemokinesCXCL12 protein, humanCXCL13 protein, humanGPR182 protein, humanReceptors, ChemokineReceptors, G-Protein-CoupledchemokineGPCRorphan

Identifiers

PMID33875597
PMCPMC8092405
OpenAlexW3154438970

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.