Evidence map›Paper›PMID 24587004›Full record

ArticlePloS one2014

Microvesicle shedding and lysosomal repair fulfill divergent cellular needs during the repair of streptolysin O-induced plasmalemmal damage.

Alexander P Atanassoff, Heidi Wolfmeier, Roman Schoenauer, Andrea Hostettler, Avi Ring, Annette Draeger, Eduard B Babiychuk

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
7.1field-weighted citation impact, top 3% 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

42 citing papers in PubMed, 68 citations in OpenAlex.

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  14. Actin Cytoskeletal Dynamics in Single-Cell Wound Repair.International journal of molecular sciences · 2021
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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 2 institutions in 2 countries.

Alexander P AtanassoffDepartment of Cell Biology, Institute of Anatomy, University of Bern, Bern, Switzerland.
Heidi WolfmeierDepartment of Cell Biology, Institute of Anatomy, University of Bern, Bern, Switzerland.
Roman SchoenauerDepartment of Cell Biology, Institute of Anatomy, University of Bern, Bern, Switzerland.
Andrea HostettlerDepartment of Cell Biology, Institute of Anatomy, University of Bern, Bern, Switzerland.
Avi RingDepartment of Protection, Norwegian Defence Research Establishment, Kjeller, Norway.
Annette DraegerDepartment of Cell Biology, Institute of Anatomy, University of Bern, Bern, Switzerland.
Eduard B BabiychukDepartment of Cell Biology, Institute of Anatomy, University of Bern, Bern, Switzerland.
University of Bern · CHNorwegian Defence Research Establishment · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathogenic bacteria secrete pore-forming toxins that permeabilize the plasma membrane of host cells. Nucleated cells possess protective mechanisms that repair toxin-damaged plasmalemma. Currently two putative repair scenarios are debated: either the isolation of the damaged membrane regions and their subsequent expulsion as microvesicles (shedding) or lysosome-dependent repair might allow the cell to rid itself of its toxic cargo and prevent lysis. Here we provide evidence that both mechanisms operate in tandem but fulfill diverse cellular needs. The prevalence of the repair strategy varies between cell types and is guided by the severity and the localization of the initial toxin-induced damage, by the morphology of a cell and, most important, by the incidence of the secondary mechanical damage. The surgically precise action of microvesicle shedding is best suited for the instant elimination of individual toxin pores, whereas lysosomal repair is indispensable for mending of self-inflicted mechanical injuries following initial plasmalemmal permeabilization by bacterial toxins. Our study provides new insights into the functioning of non-immune cellular defenses against bacterial pathogens.

Indexed as

Actin CytoskeletonBacterial ProteinsCell-Derived MicroparticlesCell Line, TumorCell MembraneCell SurvivalHEK293 CellsHumansImmunity, InnateLysosomesMembrane FusionMyosinsStreptolysinsBacterial ProteinsMyosinsstreptolysin OStreptolysins

Identifiers

PMID24587004
PMCPMC3931818
OpenAlexW2039782193

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.