Evidence map›Paper›PMID 35167863›Full record

ArticleBiophysical journal2022

Tether-guided lamellipodia enable rapid wound healing.

Elgin Korkmazhan, Andrew S Kennard, Carlos Garzon-Coral, Claudia G Vasquez, Alexander R Dunn

Open access · greenAbstract read
In one paragraph

Article in Biophysical journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 45% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
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

5 authors at 2 institutions in 1 country.

Elgin KorkmazhanGraduate Program in Biophysics, Stanford University, Stanford, California; Department of Chemical Engineering, Stanford University, Stanford, California.
Andrew S KennardDepartment of Biology and Howard Hughes Medical Institute, University of Washington, Seattle, Washington.
Carlos Garzon-CoralDepartment of Chemical Engineering, Stanford University, Stanford, California.
Claudia G VasquezDepartment of Chemical Engineering, Stanford University, Stanford, California.
Alexander R DunnDepartment of Chemical Engineering, Stanford University, Stanford, California. Electronic address: alex.dunn@stanford.edu.
Stanford University · USHoward Hughes Medical Institute · US

Funding

Molecular Biophysics Training Program at StanfordT32GM008294 · NIGMS · STANFORD UNIVERSITY · PI HUANG, KERWYN C. · 1989 to 2019
$7.4M
Molecular mechanisms underlying force transduction at cellular adhesion complexesR35GM130332 · NIGMS · STANFORD UNIVERSITY · PI Alexander R Dunn · 2019 to 2026
$4.9M
Investigating the physical mechanisms that drive multicellular lumen morphogenesisF32GM125113 · NIGMS · STANFORD UNIVERSITY · PI VASQUEZ, CLAUDIA GABRIELA · 2017 to 2018
$118k
NIGMS NIH HHS F32 GM125113NIGMS NIH HHS R35 GM130332NIGMS NIH HHS T32 GM008294
6 · The paper itself

Abstract

Adhesion between animal cells and the underlying extracellular matrix is challenged during wounding, cell division, and a variety of pathological processes. How cells recover adhesion in the immediate aftermath of detachment from the extracellular matrix remains incompletely understood, due in part to technical limitations. Here, we used acute chemical and mechanical perturbations to examine how epithelial cells respond to partial delamination events. In both cases, we found that cells extended lamellipodia to establish readhesion within seconds of detachment. These lamellipodia were guided by sparse membrane tethers whose tips remained attached to their original points of adhesion, yielding lamellipodia that appear to be qualitatively distinct from those observed during cell migration. In vivo measurements in the context of a zebrafish wound assay showed a similar behavior, in which membrane tethers guided rapidly extending lamellipodia. In the case of mechanical wounding events, cells selectively extended tether-guided lamellipodia in the direction opposite of the pulling force, resulting in the rapid reestablishment of contact with the substrate. We suggest that membrane tether-guided lamellipodial respreading may represent a general mechanism to reestablish tissue integrity in the face of acute disruption.

Indexed as

PseudopodiaZebrafishAnimalsCell MovementEpithelial CellsWound Healing

Identifiers

PMID35167863
PMCPMC8943750
OpenAlexW4211002816

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.