Evidence map›Paper›PMID 28643776›Full record

ArticleNature communications2017

Ezrin enhances line tension along transcellular tunnel edges via NMIIa driven actomyosin cable formation.

Caroline Stefani, David Gonzalez-Rodriguez, Yosuke Senju, Anne Doye, Nadia Efimova, Sébastien Janel, Justine Lipuma, Meng Chen Tsai, Daniel Hamaoui, Madhavi P Maddugoda and 7 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.6field-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

15 citing papers in PubMed, 37 citations in OpenAlex.

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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

17 authors at 6 institutions in 3 countries.

Caroline StefaniINSERM, U1065, Université de Nice-Sophia Antipolis, Centre Méditerranéen de Médecine Moléculaire (C3M), Department of microbial toxins in host-pathogen interactions, 151 Route St Antoine de Ginestière, BP 2 3194, 06204 Nice, France.
David Gonzalez-RodriguezLCP-A2MC, Institut Jean Barriol, Université de Lorraine, 1 bd Arago, Metz 57078, France.
Yosuke SenjuProgram in Cell and Molecular Biology, Institute of Biotechnology, P.O. Box 56, University of Helsinki, Helsinki 00014, Finland.
Anne DoyeINSERM, U1065, Université de Nice-Sophia Antipolis, Centre Méditerranéen de Médecine Moléculaire (C3M), Department of microbial toxins in host-pathogen interactions, 151 Route St Antoine de Ginestière, BP 2 3194, 06204 Nice, France.
Nadia EfimovaDepartment of Biology, University of Pennsylvania, 433 S. University Avenue, Philadelphia, Pennsylvania 19104, USA.
Sébastien JanelMultiscale Physics-Biology-Chemistry and Cancer, Cellular Microbiology and Physics of Infection Group, Center for Infection and Immunity of Lille, CNRS UMR8204, INSERM U1019, Institut Pasteur de Lille, Centre Hospitalier Régional de Lille, Université de Lille, Lille 59021, France.
Justine LipumaINSERM, U1065, Université de Nice-Sophia Antipolis, Centre Méditerranéen de Médecine Moléculaire (C3M), Department of microbial toxins in host-pathogen interactions, 151 Route St Antoine de Ginestière, BP 2 3194, 06204 Nice, France.
Meng Chen TsaiINSERM, U1065, Université de Nice-Sophia Antipolis, Centre Méditerranéen de Médecine Moléculaire (C3M), Department of microbial toxins in host-pathogen interactions, 151 Route St Antoine de Ginestière, BP 2 3194, 06204 Nice, France.
Daniel HamaouiINSERM, U1065, Université de Nice-Sophia Antipolis, Centre Méditerranéen de Médecine Moléculaire (C3M), Department of microbial toxins in host-pathogen interactions, 151 Route St Antoine de Ginestière, BP 2 3194, 06204 Nice, France.
Madhavi P MaddugodaINSERM, U1065, Université de Nice-Sophia Antipolis, Centre Méditerranéen de Médecine Moléculaire (C3M), Department of microbial toxins in host-pathogen interactions, 151 Route St Antoine de Ginestière, BP 2 3194, 06204 Nice, France.
Olivier Cochet-EscartinMultiscale Physics-Biology-Chemistry and Cancer, Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS, UMR168, Paris 75005, France.
Coline PrévostMultiscale Physics-Biology-Chemistry and Cancer, Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS, UMR168, Paris 75005, France.
Frank LafontMultiscale Physics-Biology-Chemistry and Cancer, Cellular Microbiology and Physics of Infection Group, Center for Infection and Immunity of Lille, CNRS UMR8204, INSERM U1019, Institut Pasteur de Lille, Centre Hospitalier Régional de Lille, Université de Lille, Lille 59021, France.
Tatyana SvitkinaDepartment of Biology, University of Pennsylvania, 433 S. University Avenue, Philadelphia, Pennsylvania 19104, USA.
Pekka LappalainenProgram in Cell and Molecular Biology, Institute of Biotechnology, P.O. Box 56, University of Helsinki, Helsinki 00014, Finland.
Patricia BassereauMultiscale Physics-Biology-Chemistry and Cancer, Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS, UMR168, Paris 75005, France.ORCID 0000-0002-8544-6778
Emmanuel LemichezINSERM, U1065, Université de Nice-Sophia Antipolis, Centre Méditerranéen de Médecine Moléculaire (C3M), Department of microbial toxins in host-pathogen interactions, 151 Route St Antoine de Ginestière, BP 2 3194, 06204 Nice, France.
Inserm · FRCentre National de la Recherche Scientifique · FRUniversity of Helsinki · FIUniversity of Pennsylvania · USLaboratoire de Chimie et Physique - Approche Multi-échelle des Milieux ComplexesVirginia Mason Medical Center · US

Funding

Multifaceted roles of nonmuscle myosin II in cell adhesion and migrationR01GM095977 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI SVITKINA, TATYANA · 2013 to 2020
$2.7M
NIGMS NIH HHS R01 GM095977
6 · The paper itself

Abstract

Transendothelial cell macroaperture (TEM) tunnels control endothelium barrier function and are triggered by several toxins from pathogenic bacteria that provoke vascular leakage. Cellular dewetting theory predicted that a line tension of uncharacterized origin works at TEM boundaries to limit their widening. Here, by conducting high-resolution microscopy approaches we unveil the presence of an actomyosin cable encircling TEMs. We develop a theoretical cellular dewetting framework to interpret TEM physical parameters that are quantitatively determined by laser ablation experiments. This establishes the critical role of ezrin and non-muscle myosin II (NMII) in the progressive implementation of line tension. Mechanistically, fluorescence-recovery-after-photobleaching experiments point for the upstream role of ezrin in stabilizing actin filaments at the edges of TEMs, thereby favouring their crosslinking by NMIIa. Collectively, our findings ascribe to ezrin and NMIIa a critical function of enhancing line tension at the cell boundary surrounding the TEMs by promoting the formation of an actomyosin ring.

Indexed as

Actin CytoskeletonActomyosinCytoskeletal ProteinsEzrinHumansHuman Umbilical Vein Endothelial CellsNonmuscle Myosin Type IIASurface TensionActomyosinCytoskeletal ProteinsEzrinNonmuscle Myosin Type IIA

Identifiers

PMID28643776
PMCPMC5490010
OpenAlexW2687627042

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.