Evidence map›Paper›PMID 27173494›Full record

ArticleJournal of cell science2016

Lamellipodia are crucial for haptotactic sensing and response.

Samantha J King, Sreeja B Asokan, Elizabeth M Haynes, Seth P Zimmerman, Jeremy D Rotty, James G Alb, Alicia Tagliatela, Devon R Blake, Irina P Lebedeva, Daniel Marston and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cell science, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

52 citing papers in PubMed, 86 citations in OpenAlex.

  1. Article
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  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. The Arp2/3 complex is required forbioRxiv : the preprint server for biology · 2025
    Article
  12. Article
  13. Haptotactic Motion of Multivalent Vesicles Along Ligand-Density Gradients.Langmuir : the ACS journal of surfaces and colloids · 2025
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
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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

16 authors at 3 institutions in 2 countries.

Samantha J KingUNC Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27514, USA Department of Cell Biology and Physiology, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Sreeja B AsokanUNC Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27514, USA Department of Cell Biology and Physiology, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Elizabeth M HaynesUNC Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27514, USA Department of Cell Biology and Physiology, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Seth P ZimmermanUNC Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27514, USA Department of Biochemistry and Biophysics, University of North Carolina, Chapel Hill, NC 27599, USA.
Jeremy D RottyUNC Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27514, USA Department of Cell Biology and Physiology, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
James G AlbUNC Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27514, USA Department of Cell Biology and Physiology, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Alicia TagliatelaUNC Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27514, USA Department of Cell Biology and Physiology, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Devon R BlakeUNC Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27514, USA Department of Pharmacology, University of North Carolina at Chapel Hill, School of Medicine, Chapel Hill, NC 27599, USA.
Irina P LebedevaUNC Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27514, USA Howard Hughes Medical Institute, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Daniel MarstonDepartment of Pharmacology, University of North Carolina at Chapel Hill, School of Medicine, Chapel Hill, NC 27599, USA.
Heath E JohnsonDepartment of Chemical & Biomolecular Engineering, North Carolina State University, Raleigh, NC 27695, USA.
Maddy ParsonsKing's College London, Randall Institute, London SE1 8RT, UK.
Norman E SharplessUNC Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27514, USA Department of Genetics, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Brian KuhlmanUNC Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27514, USA Department of Biochemistry and Biophysics, University of North Carolina, Chapel Hill, NC 27599, USA.
Jason M HaughDepartment of Chemical & Biomolecular Engineering, North Carolina State University, Raleigh, NC 27695, USA.
James E BearUNC Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27514, USA Department of Cell Biology and Physiology, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA Howard Hughes Medical Institute, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA jbear@email.unc.edu.ORCID 0000-0002-8489-996X
University of North Carolina at Chapel Hill · USNorth Carolina State University · USKing's College London · GB

Funding

Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Deborah F. Tate · 1985 to 2026
$201.5M
CANCER CELL BIOLOGY TRAINING PROGRAMT32CA071341 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CHANNING J. DER, Yuliya Pylayeva-Gupta · 1996 to 2026
$5.0M
Multiscale Modeling of Wound HealingU01EB018816 · NIBIB · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI HAUGH, JASON M. · 2014 to 2021
$4.0M
Spatiotemporal Control of the Epigenome via Photoactivatable Nuclear LocalizationR01DA036877 · NIDA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HAHN, KLAUS M., KUHLMAN, BRIAN A · 2013 to 2017
$2.1M
In vivo murine models of metastasis for therapeutic testingR01CA163896 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SHARPLESS, NORMAN E, WONG, KWOK KIN · 2012 to 2016
$2.0M
The role of the Arp2/3 complex in cellular actin dynamicsR01GM111557 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BEAR, JAMES E · 2014 to 2018
$1.5M
Mechanisms of mesenchymal chemotaxisR01GM110155 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BEAR, JAMES E, HAUGH, JASON M. · 2014 to 2017
$1.4M
Design of Genetically Encoded Photoactivatable ProteinsR01GM093208 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KUHLMAN, BRIAN A · 2010 to 2013
$1.1M
NCI NIH HHS P30 CA016086NCI NIH HHS R01 CA163896NCI NIH HHS T32 CA071341NIBIB NIH HHS U01 EB018816NIDA NIH HHS R01 DA036877NIGMS NIH HHS R01 GM093208NIGMS NIH HHS R01 GM110155NIGMS NIH HHS R01 GM111557
6 · The paper itself

Abstract

Haptotaxis is the process by which cells respond to gradients of substrate-bound cues, such as extracellular matrix proteins (ECM); however, the cellular mechanism of this response remains poorly understood and has mainly been studied by comparing cell behavior on uniform ECMs with different concentrations of components. To study haptotaxis in response to gradients, we utilized microfluidic chambers to generate gradients of the ECM protein fibronectin, and imaged the cell migration response. Lamellipodia are fan-shaped protrusions that are common in migrating cells. Here, we define a new function for lamellipodia and the cellular mechanism required for haptotaxis - differential actin and lamellipodial protrusion dynamics lead to biased cell migration. Modest differences in lamellipodial dynamics occurring over time periods of seconds to minutes are summed over hours to produce differential whole cell movement towards higher concentrations of fibronectin. We identify a specific subset of lamellipodia regulators as being crucial for haptotaxis. Numerous studies have linked components of this pathway to cancer metastasis and, consistent with this, we find that expression of the oncogenic Rac1 P29S mutation abrogates haptotaxis. Finally, we show that haptotaxis also operates through this pathway in 3D environments.

Indexed as

ChemotaxisActin-Related Protein 2-3 ComplexActinsAnimalsFibroblastsFibronectinsFocal Adhesion Protein-Tyrosine KinasesFocal AdhesionsGuanine Nucleotide Exchange FactorsIntegrin beta1MiceModels, BiologicalPseudopodiarac GTP-Binding ProteinsSignal Transductionsrc-Family KinasesActin-Related Protein 2-3 ComplexActinsFibronectinsFocal Adhesion Protein-Tyrosine KinasesGuanine Nucleotide Exchange FactorsIntegrin beta1rac GTP-Binding Proteinssrc-Family KinasesTiam1 protein, mouseT-Lymphoma Invasion and Metastasis-inducing Protein 1Wiskott-Aldrich Syndrome ProteinWiskott-Aldrich Syndrome Protein FamilyArp2/3Directed migrationHaptotaxisLamellipodia

Identifiers

PMID27173494
PMCPMC4920251
OpenAlexW2350539200

What OpenQuestion holds

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Registered trials

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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.