Evidence map›Paper›PMID 33597528›Full record

ArticleNature communications2021

Dissection of intercellular communication using the transcriptome-based framework ICELLNET.

Floriane Noël, Lucile Massenet-Regad, Irit Carmi-Levy, Antonio Cappuccio, Maximilien Grandclaudon, Coline Trichot, Yann Kieffer, Fatima Mechta-Grigoriou, Vassili Soumelis

Abstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 138 papers.

0numbers the graph read from it
0cells of the map it votes in
138citing papers in PubMed
–field-weighted citation impact
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

138 citing papers in PubMed.

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

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

9 authors.

Floriane Noël *Université de Paris, INSERM U976, Equipe labellisée par la Ligue Nationale contre le Cancer, F-75006 Paris, France.ORCID 0000-0001-8813-4780
Lucile Massenet-Regad *Université de Paris, INSERM U976, Equipe labellisée par la Ligue Nationale contre le Cancer, F-75006 Paris, France.ORCID 0000-0003-1629-8983
Irit Carmi-LevyInstitut Curie, 26 rue d'Ulm, Paris, France.
Antonio CappuccioInstitut Curie, 26 rue d'Ulm, Paris, France.
Maximilien GrandclaudonInstitut Curie, 26 rue d'Ulm, Paris, France.
Coline TrichotUniversité de Paris, INSERM U976, Equipe labellisée par la Ligue Nationale contre le Cancer, F-75006 Paris, France.
Yann KiefferInstitut Curie, 26 rue d'Ulm, Paris, France.ORCID 0000-0003-2722-3071
Fatima Mechta-GrigoriouInstitut Curie, 26 rue d'Ulm, Paris, France.ORCID 0000-0002-3751-6989
Vassili SoumelisUniversité de Paris, INSERM U976, Equipe labellisée par la Ligue Nationale contre le Cancer, F-75006 Paris, France. vassili.soumelis@aphp.fr.ORCID 0000-0003-1849-9834

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell-to-cell communication can be inferred from ligand-receptor expression in cell transcriptomic datasets. However, important challenges remain: global integration of cell-to-cell communication; biological interpretation; and application to individual cell population transcriptomic profiles. We develop ICELLNET, a transcriptomic-based framework integrating: 1) an original expert-curated database of ligand-receptor interactions accounting for multiple subunits expression; 2) quantification of communication scores; 3) the possibility to connect a cell population of interest with 31 reference human cell types; and 4) three visualization modes to facilitate biological interpretation. We apply ICELLNET to three datasets generated through RNA-seq, single-cell RNA-seq, and microarray. ICELLNET reveals autocrine IL-10 control of human dendritic cell communication with up to 12 cell types. Four of them (T cells, keratinocytes, neutrophils, pDC) are further tested and experimentally validated. In summary, ICELLNET is a global, versatile, biologically validated, and easy-to-use framework to dissect cell communication from individual or multiple cell-based transcriptomic profiles.

Indexed as

Databases, FactualAnimalsCell CommunicationCells, CulturedComputational BiologyDendritic CellsGene Expression ProfilingHumansKeratinocytesNeutrophilsSequence Analysis, RNASingle-Cell AnalysisT-LymphocytesTranscriptome

Identifiers

PMID33597528
PMCPMC7889941

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Registered trials

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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.