Evidence map›Paper›PMID 35148838›Full record

ArticleCell2022

GPR35 promotes neutrophil recruitment in response to serotonin metabolite 5-HIAA.

Marco De Giovanni, Hanson Tam, Colin Valet, Ying Xu, Mark R Looney, Jason G Cyster

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Cell, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 89 papers.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed
12.8field-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

89 citing papers in PubMed, 155 citations in OpenAlex.

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  12. Platelet effector functions in inflammation.Research and practice in thrombosis and haemostasis · 2026
    Review
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  19. GPCRs as key regulators in wound healing.Frontiers in cell and developmental biology · 2026
    Review
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Marco De GiovanniHoward Hughes Medical Institute, Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA 94143, USA. Electronic address: marco.degiovanni@ucsf.edu.
Hanson TamHoward Hughes Medical Institute, Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA 94143, USA.
Colin ValetDepartments of Medicine and Laboratory Medicine, University of California, San Francisco, San Francisco, CA 94143, USA.
Ying XuHoward Hughes Medical Institute, Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA 94143, USA.
Mark R LooneyDepartments of Medicine and Laboratory Medicine, University of California, San Francisco, San Francisco, CA 94143, USA.
Jason G CysterHoward Hughes Medical Institute, Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA 94143, USA. Electronic address: jason.cyster@ucsf.edu.
Howard Hughes Medical Institute · USUniversity of California, San Francisco · US

Funding

Chemokines and Lymphoid Tissue Organization and FunctionR01AI045073 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CYSTER, JASON G · 1999 to 2023
$7.6M
B LYMPHOCYTE MIGRATION AND HOMEOSTASISR01AI040098 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Jason G Cyster · 1997 to 2026
$7.0M
Immunobiology of the normal and injured lungR35HL161241 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MARK ROBERTS LOONEY · 2022 to 2026
$4.2M
Mechanisms and pathogenicity of SARS-CoV-2-induced neutrophil extracellular trapsR01AI160167 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LOONEY, MARK ROBERTS · 2021 to 2025
$3.1M
Fine-tuning the Neutrophilic Response to PneumoniaR01AI125445 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LOONEY, MARK ROBERTS · 2016 to 2020
$2.2M
Chemokines and Lymphoid Tissue Organization and FunctionR37AI045073 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Jason G Cyster · 2024 to 2026
$1.7M
GPR35 function in the immune systemR21AI163036 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CYSTER, JASON G · 2021 to 2022
$444k
NHLBI NIH HHS R35 HL161241NIAID NIH HHS N01 AI040098NIAID NIH HHS R01 AI040098NIAID NIH HHS R01 AI045073NIAID NIH HHS R01 AI125445NIAID NIH HHS R01 AI160167NIAID NIH HHS R21 AI163036NIAID NIH HHS R37 AI045073
6 · The paper itself

Abstract

Rapid neutrophil recruitment to sites of inflammation is crucial for innate immune responses. Here, we reveal that the G-protein-coupled receptor GPR35 is upregulated in activated neutrophils, and it promotes their migration. GPR35-deficient neutrophils are less recruited from blood vessels into inflamed tissue, and the mice are less efficient in clearing peritoneal bacteria. Using a bioassay, we find that serum and activated platelet supernatant stimulate GPR35, and we identify the platelet-derived serotonin metabolite 5-hydroxyindoleacetic acid (5-HIAA) as a GPR35 ligand. GPR35 function in neutrophil recruitment is strongly dependent on platelets, with the receptor promoting transmigration across platelet-coated endothelium. Mast cells also attract GPR35

Indexed as

NeutrophilsAnimalsHydroxyindoleacetic AcidInflammationLigandsMiceNeutrophil InfiltrationReceptors, G-Protein-CoupledSerotoninGPR35 protein, mouseHydroxyindoleacetic AcidLigandsReceptors, G-Protein-CoupledSerotonin5-HIAAGPCRsGPR35inflammationmast cellsmigrationneutrophilplateletsserotonin metaboliteSSRI

Identifiers

PMID35148838
PMCPMC9037118
OpenAlexW4211205596

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.