Evidence map›Paper›PMID 25532521›Full record

ArticleMolecular & cellular proteomics : MCP2015

Integrating phosphoproteome and transcriptome reveals new determinants of macrophage multinucleation.

Maxime Rotival, Jeong-Hun Ko, Prashant K Srivastava, Audrey Kerloc'h, Alex Montoya, Claudio Mauro, Peter Faull, Pedro R Cutillas, Enrico Petretto, Jacques Behmoaras

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

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  18. Macrophage epoxygenase determines a profibrotic transcriptome signature.Journal of immunology (Baltimore, Md. : 1950) · 2015
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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

10 authors at 2 institutions in 1 country.

Maxime RotivalFrom the ‡Integrative Genomics and Medicine, MRC Clinical Sciences Centre, Imperial College London, UK;
Jeong-Hun Ko§Centre for Complement and Inflammation Research (CCIR), Imperial College London, UK;
Prashant K SrivastavaFrom the ‡Integrative Genomics and Medicine, MRC Clinical Sciences Centre, Imperial College London, UK;
Audrey Kerloc'h§Centre for Complement and Inflammation Research (CCIR), Imperial College London, UK;
Alex Montoya‖Biological Mass Spectrometry and Proteomics Laboratory, MRC Clinical Sciences Centre, Imperial College London, UK;
Claudio Mauro¶William Harvey Research Institute, Queen Mary University of London, UK;
Peter Faull‖Biological Mass Spectrometry and Proteomics Laboratory, MRC Clinical Sciences Centre, Imperial College London, UK;
Pedro R Cutillas**Integrative Cell Signaling and Proteomics, Barts Cancer Institute, Queen Mary University of London, UK.
Enrico PetrettoFrom the ‡Integrative Genomics and Medicine, MRC Clinical Sciences Centre, Imperial College London, UK; Jacquesb@imperial.ac.uk enrico.petretto@duke-nus.edu.sg.
Jacques Behmoaras§Centre for Complement and Inflammation Research (CCIR), Imperial College London, UK; Jacquesb@imperial.ac.uk enrico.petretto@duke-nus.edu.sg.
Imperial College London · GBQueen Mary University of London · GB

Funding

British Heart Foundation FS/12/38/29640Medical Research Council MC_U120097112Medical Research Council MR/M004716/1
6 · The paper itself

Abstract

Macrophage multinucleation (MM) is essential for various biological processes such as osteoclast-mediated bone resorption and multinucleated giant cell-associated inflammatory reactions. Here we study the molecular pathways underlying multinucleation in the rat through an integrative approach combining MS-based quantitative phosphoproteomics (LC-MS/MS) and transcriptome (high-throughput RNA-sequencing) to identify new regulators of MM. We show that a strong metabolic shift toward HIF1-mediated glycolysis occurs at transcriptomic level during MM, together with modifications in phosphorylation of over 50 proteins including several ARF GTPase activators and polyphosphate inositol phosphatases. We use shortest-path analysis to link differential phosphorylation with the transcriptomic reprogramming of macrophages and identify LRRFIP1, SMARCA4, and DNMT1 as novel regulators of MM. We experimentally validate these predictions by showing that knock-down of these latter reduce macrophage multinucleation. These results provide a new framework for the combined analysis of transcriptional and post-translational changes during macrophage multinucleation, prioritizing essential genes, and revealing the sequential events leading to the multinucleation of macrophages.

Indexed as

AnimalsCell NucleusCells, CulturedDNA (Cytosine-5-)-Methyltransferase 1DNA (Cytosine-5-)-MethyltransferasesDNA HelicasesGene Expression ProfilingHigh-Throughput Nucleotide SequencingMacrophagesNuclear ProteinsPhosphorylationProteomeRatsRats, Inbred LewRats, Inbred WKYRNA-Binding ProteinsDNA (Cytosine-5-)-Methyltransferase 1DNA (Cytosine-5-)-MethyltransferasesDNA HelicasesDnmt1 protein, ratLRRFIP1 protein, ratNuclear ProteinsProteomeRNA-Binding ProteinsSmarca4 protein, ratTranscription Factors

Identifiers

PMID25532521
PMCPMC4349971
OpenAlexW2018359792

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.