Evidence map›Paper›PMID 37672339›Full record

ArticleMolecular biology of the cell2023

Nascent adhesions shorten the period of lamellipodium protrusion through the Brownian ratchet mechanism.

Keith R Carney, Akib M Khan, Samantha Stam, Shiela C Samson, Nikhil Mittal, Sangyoon J Han, Tamara C Bidone, Michelle C Mendoza

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. ERK builds a population of short-lived nascent adhesions that produce persistent edge protrusion and cell migration.Proceedings of the National Academy of Sciences of the United States of America · 2026
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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

8 authors at 2 institutions in 1 country.

Keith R CarneyDepartment of Oncological Sciences, University of Utah, Salt Lake City, UT 84112.
Akib M KhanDepartment of Oncological Sciences, University of Utah, Salt Lake City, UT 84112.
Samantha StamDepartment of Oncological Sciences, University of Utah, Salt Lake City, UT 84112.
Shiela C SamsonDepartment of Oncological Sciences, University of Utah, Salt Lake City, UT 84112.
Nikhil MittalDepartment of Biomedical Engineering, Michigan Technological University, Houghton, MI 49931.
Sangyoon J HanDepartment of Biomedical Engineering, Michigan Technological University, Houghton, MI 49931.
Tamara C BidoneDepartment of Biomedical Engineering, University of Utah, Salt Lake City, UT 84112.ORCID 0000-0002-7096-4839
Michelle C MendozaDepartment of Oncological Sciences, University of Utah, Salt Lake City, UT 84112.ORCID 0000-0002-6490-1794
University of Utah · USMichigan Technological University · US

Funding

Computational models of cell mechanosensing through integrin-based adhesionsR35GM147491 · NIGMS · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Tamara Bidone · 2022 to 2026
$1.9M
Kinase Control of Synergistic Cell Migration MechanicsR01GM141372 · NIGMS · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Michelle Christine Mendoza · 2022 to 2026
$1.6M
Nascent Adhesion-Based Mechano-transmission for Extracellular Matrix Stiffness SensingR15GM135806 · NIGMS · MICHIGAN TECHNOLOGICAL UNIVERSITY · PI HAN, SANGYOON JOSHUA · 2019 to 2024
$964k
NIGMS NIH HHS R01 GM141372NIGMS NIH HHS R15 GM135806NIGMS NIH HHS R35 GM147491
6 · The paper itself

Abstract

Directional cell migration is driven by the conversion of oscillating edge motion into lasting periods of leading edge protrusion. Actin polymerization against the membrane and adhesions control edge motion, but the exact mechanisms that determine protrusion period remain elusive. We addressed this by developing a computational model in which polymerization of actin filaments against a deformable membrane and variable adhesion dynamics support edge motion. Consistent with previous reports, our model showed that actin polymerization and adhesion lifetime power protrusion velocity. However, increasing adhesion lifetime decreased the protrusion period. Measurements of adhesion lifetime and edge motion in migrating cells confirmed that adhesion lifetime is associated with and promotes protrusion velocity, but decreased duration. Our model showed that adhesions' control of protrusion persistence originates from the Brownian ratchet mechanism for actin filament polymerization. With longer adhesion lifetime or increased-adhesion density, the proportion of actin filaments tethered to the substrate increased, maintaining filaments against the cell membrane. The reduced filament-membrane distance generated pushing force for high edge velocity, but limited further polymerization needed for protrusion duration. We propose a mechanism for cell edge protrusion in which adhesion strength regulates actin filament polymerization to control the periods of leading edge protrusion.

Indexed as

ActinsModels, BiologicalActin CytoskeletonCell MovementPseudopodiaActins

Identifiers

PMID37672339
PMCPMC10846621
OpenAlexW4386485640

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.