Evidence map›Paper›PMID 32241914›Full record

ArticleThe Journal of biological chemistry2020

Phosphoproteomic characterization of the signaling network resulting from activation of the chemokine receptor CCR2.

Cheng Huang, Simon R Foster, Anup D Shah, Oded Kleifeld, Meritxell Canals, Ralf B Schittenhelm, Martin J Stone

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Monocyte Migration Emerges from a Divergent Chemokine Signaling Network.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. GCN2 mediates access to stored amino acids for somatic maintenance duringbioRxiv : the preprint server for biology · 2023
    Article
  5. Review
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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

7 authors at 4 institutions in 4 countries.

Cheng HuangInfection and Immunity Program and Department of Biochemistry and Molecular Biology, Monash Biomedicine Discovery Institute, Monash University, Clayton 3800, Victoria, Australia.ORCID 0000-0002-4575-1233
Simon R FosterInfection and Immunity Program and Department of Biochemistry and Molecular Biology, Monash Biomedicine Discovery Institute, Monash University, Clayton 3800, Victoria, Australia.
Anup D ShahInfection and Immunity Program and Department of Biochemistry and Molecular Biology, Monash Biomedicine Discovery Institute, Monash University, Clayton 3800, Victoria, Australia.
Oded KleifeldFaculty of Biology, Technion-Israel Institute of Technology, Technion City, Haifa 3200003, Israel.
Meritxell CanalsDivision of Physiology, Pharmacology and Neuroscience, School of Life Sciences, Queen's Medical Centre, University of Nottingham, Nottingham NG7 2UH, United Kingdom.ORCID 0000-0002-7942-5006
Ralf B SchittenhelmInfection and Immunity Program and Department of Biochemistry and Molecular Biology, Monash Biomedicine Discovery Institute, Monash University, Clayton 3800, Victoria, Australia ralf.schittenhelm@monash.edu.ORCID 0000-0001-8738-1878
Martin J StoneInfection and Immunity Program and Department of Biochemistry and Molecular Biology, Monash Biomedicine Discovery Institute, Monash University, Clayton 3800, Victoria, Australia martin.stone@monash.edu.ORCID 0000-0002-6468-4427
Australian Regenerative Medicine Institute · AUDiscovery Institute · USTechnion – Israel Institute of Technology · ILUniversity of Nottingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Leukocyte recruitment is a universal feature of tissue inflammation and regulated by the interactions of chemokines with their G protein-coupled receptors. Activation of CC chemokine receptor 2 (CCR2) by its cognate chemokine ligands, including CC chemokine ligand 2 (CCL2), plays a central role in recruitment of monocytes in several inflammatory diseases. In this study, we used phosphoproteomics to conduct an unbiased characterization of the signaling network resulting from CCL2 activation of CCR2. Using data-independent acquisition MS analysis, we quantified both the proteome and phosphoproteome in FlpIn-HEK293T cells stably expressing CCR2 at six time points after activation with CCL2. Differential expression analysis identified 699 significantly regulated phosphorylation sites on 441 proteins. As expected, many of these proteins are known to participate in canonical signal transduction pathways and in the regulation of actin cytoskeleton dynamics, including numerous guanine nucleotide exchange factors and GTPase-activating proteins. Moreover, we identified regulated phosphorylation sites in numerous proteins that function in the nucleus, including several constituents of the nuclear pore complex. The results of this study provide an unprecedented level of detail of CCR2 signaling and identify potential targets for regulation of CCR2 function.

Indexed as

ProteomicsSignal TransductionGene OntologyHEK293 CellsHumansPhosphoproteinsPhosphorylationReceptors, CCR2PhosphoproteinsReceptors, CCR2actinC-C chemokine ligand type 2 (CCL2)C-C chemokine receptor type 2 (CCR2)CCL2CCR2cell signalingchemokinecytoskeletondata-independent acquisitiondata-independent acquisition mass spectrometry (DIA-MS)G protein-coupled receptor (GPCR)GTPase-activating protein (GAP)guanine nucleotide exchange factor (GEF)mass spectrometry (MS)nuclear porephosphoproteomicssignaling networks

Identifiers

PMID32241914
PMCPMC7212651
OpenAlexW3014666648

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.