Evidence map›Paper›PMID 32282802›Full record

ArticlePloS one2020

Quasi-periodic migration of single cells on short microlanes.

Fang Zhou, Sophia A Schaffer, Christoph Schreiber, Felix J Segerer, Andriy Goychuk, Erwin Frey, Joachim O Rädler

Abstract read
In one paragraph

Article in PloS one, 2020. 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
–field-weighted citation impact
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.

  1. Mesenchymal cell migration on one-dimensional micropatterns.Frontiers in cell and developmental biology · 2024
    Review
  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

7 authors.

Fang ZhouFaculty of Physics and Center for NanoScience, Ludwig-Maximilians-Universität München, Munich, Germany.
Sophia A SchafferFaculty of Physics and Center for NanoScience, Ludwig-Maximilians-Universität München, Munich, Germany.
Christoph SchreiberFaculty of Physics and Center for NanoScience, Ludwig-Maximilians-Universität München, Munich, Germany.
Felix J SegererFaculty of Physics and Center for NanoScience, Ludwig-Maximilians-Universität München, Munich, Germany.
Andriy GoychukArnold-Sommerfeld-Center for Theoretical Physics, Faculty of Physics and Center for NanoScience, Ludwig-Maximilians-Universität München, Munich, Germany.ORCID 0000-0001-6776-9437
Erwin FreyArnold-Sommerfeld-Center for Theoretical Physics, Faculty of Physics and Center for NanoScience, Ludwig-Maximilians-Universität München, Munich, Germany.
Joachim O RädlerFaculty of Physics and Center for NanoScience, Ludwig-Maximilians-Universität München, Munich, Germany.ORCID 0000-0002-5846-1489

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell migration on microlanes represents a suitable and simple platform for the exploration of the molecular mechanisms underlying cell cytoskeleton dynamics. Here, we report on the quasi-periodic movement of cells confined in stripe-shaped microlanes. We observe persistent polarized cell shapes and directed pole-to-pole motion within the microlanes. Cells depolarize at one end of a given microlane, followed by delayed repolarization towards the opposite end. We analyze cell motility via the spatial velocity distribution, the velocity frequency spectrum and the reversal time as a measure for depolarization and spontaneous repolarization of cells at the microlane ends. The frequent encounters of a boundary in the stripe geometry provides a robust framework for quantitative investigations of the cytoskeleton protrusion and repolarization dynamics. In a first advance to rigorously test physical models of cell migration, we find that the statistics of the cell migration is recapitulated by a Cellular Potts model with a minimal description of cytoskeleton dynamics. Using LifeAct-GFP transfected cells and microlanes with differently shaped ends, we show that the local deformation of the leading cell edge in response to the tip geometry can locally either amplify or quench actin polymerization, while leaving the average reversal times unaffected.

Indexed as

Cell MovementMicrotechnologyCell Line, TumorCytoskeletonHumansSingle-Cell Analysis

Identifiers

PMID32282802
PMCPMC7153896

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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.