Evidence map›Paper›PMID 38102112›Full record

ArticleNature communications2023

Rho GTPase activity crosstalk mediated by Arhgef11 and Arhgef12 coordinates cell protrusion-retraction cycles.

Suchet Nanda, Abram Calderon, Arya Sachan, Thanh-Thuy Duong, Johannes Koch, Xiaoyi Xin, Djamschid Solouk-Stahlberg, Yao-Wen Wu, Perihan Nalbant, Leif Dehmelt

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

25 citing papers in PubMed, 37 citations in OpenAlex.

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  6. Tissue signatures of human macrophages during homeostasis and activation.Journal of immunology (Baltimore, Md. : 1950) · 2026
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  9. Decoding Rho GTPase signalling networks in directed cell migration.Frontiers in cell and developmental biology · 2026
    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

10 authors at 3 institutions in 2 countries.

Suchet Nanda *Fakultät für Chemie und Chemische Biologie, TU Dortmund University, 44227, Dortmund, Germany.ORCID http://orcid.org/0000-0001-9863-8069
Abram Calderon *Fakultät für Chemie und Chemische Biologie, TU Dortmund University, 44227, Dortmund, Germany.
Arya Sachan *Fakultät für Chemie und Chemische Biologie, TU Dortmund University, 44227, Dortmund, Germany.ORCID http://orcid.org/0009-0006-3631-9648
Thanh-Thuy Duong *Fakultät für Chemie und Chemische Biologie, TU Dortmund University, 44227, Dortmund, Germany.
Johannes KochDepartment of Molecular Cell Biology, Center of Medical Biotechnology, University of Duisburg-Essen, 45141, Essen, Germany.
Xiaoyi XinSciLifeLab and Department of Chemistry, Umeå Centre for Microbial Research, Umeå University, 90187, Umeå, Sweden.
Djamschid Solouk-StahlbergFakultät für Chemie und Chemische Biologie, TU Dortmund University, 44227, Dortmund, Germany.
Yao-Wen WuSciLifeLab and Department of Chemistry, Umeå Centre for Microbial Research, Umeå University, 90187, Umeå, Sweden.ORCID http://orcid.org/0000-0002-2573-8736
Perihan NalbantDepartment of Molecular Cell Biology, Center of Medical Biotechnology, University of Duisburg-Essen, 45141, Essen, Germany. perihan.nalbant@uni-due.de.ORCID http://orcid.org/0000-0002-5649-5933
Leif DehmeltFakultät für Chemie und Chemische Biologie, TU Dortmund University, 44227, Dortmund, Germany. leif.dehmelt@tu-dortmund.de.ORCID http://orcid.org/0000-0002-6559-6496
TU Dortmund University · DEScience for Life Laboratory · SEUniversity of Duisburg-Essen · DE

Funding

Bundesministerium für Bildung und Forschung (Federal Ministry of Education and Research) 0315258Deutsche Forschungsgemeinschaft (German Research Foundation) 823/10-1Deutsche Forschungsgemeinschaft (German Research Foundation) 823/4-1Deutsche Forschungsgemeinschaft (German Research Foundation) 823/8-1Deutsche Forschungsgemeinschaft (German Research Foundation) 823/9-1Deutscher Akademischer Austauschdienst (German Academic Exchange Service) Ph.D. fellowship
6 · The paper itself

Abstract

Rho GTPases play a key role in the spatio-temporal coordination of cytoskeletal dynamics during cell migration. Here, we directly investigate crosstalk between the major Rho GTPases Rho, Rac and Cdc42 by combining rapid activity perturbation with activity measurements in mammalian cells. These studies reveal that Rac stimulates Rho activity. Direct measurement of spatio-temporal activity patterns show that Rac activity is tightly and precisely coupled to local cell protrusions, followed by Rho activation during retraction. Furthermore, we find that the Rho-activating Lbc-type GEFs Arhgef11 and Arhgef12 are enriched at transient cell protrusions and retractions and recruited to the plasma membrane by active Rac. In addition, their depletion reduces activity crosstalk, cell protrusion-retraction dynamics and migration distance and increases migration directionality. Thus, our study shows that Arhgef11 and Arhgef12 facilitate exploratory cell migration by coordinating cell protrusion and retraction by coupling the activity of the associated regulators Rac and Rho.

Indexed as

Cell Sizerho GTP-Binding ProteinsAnimalscdc42 GTP-Binding ProteinCell MembraneCell MovementCytoskeletonGuanine Nucleotide Exchange FactorsMammalscdc42 GTP-Binding ProteinGuanine Nucleotide Exchange Factorsrho GTP-Binding Proteins

Identifiers

PMID38102112
PMCPMC10724141
OpenAlexW4389783851

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.