Evidence map›Paper›PMID 23979717›Full record

ArticleThe Journal of cell biology2013

Distinct signaling mechanisms regulate migration in unconfined versus confined spaces.

Wei-Chien Hung, Shih-Hsun Chen, Colin D Paul, Kimberly M Stroka, Ying-Chun Lo, Joy T Yang, Konstantinos Konstantopoulos

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed
8.8field-weighted citation impact, top 1% 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

89 citing papers in PubMed, 153 citations in OpenAlex.

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  17. Hydrogels for Salivary Gland Tissue Engineering.Gels (Basel, Switzerland) · 2022
    Review
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  20. Review

29 more citing papers are in PubMed but not listed here.

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 1 country.

Wei-Chien HungDepartment of Chemical and Biomolecular Engineering, School of Medicine, Johns Hopkins University, Baltimore, MD 21218, USA.
Shih-Hsun Chen
Colin D Paul
Kimberly M Stroka
Ying-Chun Lo
Joy T Yang
Konstantinos Konstantopoulos
Johns Hopkins University · USPhysical Sciences (United States) · US

Funding

TRANS NETWORK PROJECTSU54CA143868 · NCI · JOHNS HOPKINS UNIVERSITY · PI WIRTZ, DENIS · 2009 to 2013
$13.7M
T32: Predoctoral and Postdoctoral Training Program in Nanotechnology for Cancer ResearchT32CA153952 · NCI · JOHNS HOPKINS UNIVERSITY · PI Denis Wirtz · 2015 to 2026
$3.5M
Molecular Characterization of Cell-Cell Interactions in Cancer MetastasisR01CA101135 · NCI · JOHNS HOPKINS UNIVERSITY · PI KONSTANTOPOULOS, KONSTANTINOS · 2003 to 2011
$2.5M
How Does a4B1 Integrin Regulate Cell Migration?R01GM063710 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI YANG, JOY · 2003 to 2010
$2.1M
T-32 NIH Postdoctoral Training Program in Nanotechnology for Cancer Medicine NTCMT32CA130840 · NCI · JOHNS HOPKINS UNIVERSITY · PI WIRTZ, DENIS · 2008 to 2012
$1.2M
Molecular Characterization of Cell-Cell Interactions in Cancer MetastasisR56CA101135 · NCI · JOHNS HOPKINS UNIVERSITY · PI KONSTANTOPOULOS, KONSTANTINOS · 2007 to 2007
$295k
Role of the physical microenvironment in tumor cell migration and the cell cycleF32CA177756 · NCI · JOHNS HOPKINS UNIVERSITY · PI STROKA, KIMBERLY · 2013 to 2014
$93k
NCI NIH HHS CA101135NCI NIH HHS F32 CA177756NCI NIH HHS F32-CA177756NCI NIH HHS R01 CA101135NCI NIH HHS R56 CA101135NCI NIH HHS T32 CA130840NCI NIH HHS T32 CA153952NCI NIH HHS U54 CA143868NCI NIH HHS U54-CA143868NIGMS NIH HHS GM63710NIGMS NIH HHS R01 GM063710
6 · The paper itself

Abstract

Using a microchannel assay, we demonstrate that cells adopt distinct signaling strategies to modulate cell migration in different physical microenvironments. We studied α4β1 integrin-mediated signaling, which regulates cell migration pertinent to embryonic development, leukocyte trafficking, and melanoma invasion. We show that α4β1 integrin promotes cell migration through both unconfined and confined spaces. However, unlike unconfined (2D) migration, which depends on enhanced Rac1 activity achieved by preventing α4/paxillin binding, confined migration requires myosin II-driven contractility, which is increased when Rac1 is inhibited by α4/paxillin binding. This Rac1-myosin II cross talk mechanism also controls migration of fibroblast-like cells lacking α4β1 integrin, in which Rac1 and myosin II modulate unconfined and confined migration, respectively. We further demonstrate the distinct roles of myosin II isoforms, MIIA and MIIB, which are primarily required for confined and unconfined migration, respectively. This work provides a paradigm for the plasticity of cells migrating through different physical microenvironments.

Indexed as

Cell MovementSignal Transduction3T3 CellsAnimalsCell Line, TumorCHO CellsCricetinaeCricetulusFocal AdhesionsHeterocyclic Compounds, 4 or More RingsHumansIntegrin alpha4Integrin alpha4beta1Jurkat CellsMelanomaMiceblebbistatinHeterocyclic Compounds, 4 or More RingsIntegrin alpha4Integrin alpha4beta1Mutant ProteinsMyosin Type IIPaxillinrac1 GTP-Binding ProteinrhoA GTP-Binding Protein

Identifiers

PMID23979717
PMCPMC3760608
OpenAlexW2041651184

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.