Evidence map›Paper›PMID 22629471›Full record

ArticlePloS one2012

Paxillin and Hic-5 interaction with vinculin is differentially regulated by Rac1 and RhoA.

Nicholas O Deakin, Christoph Ballestrem, Christopher E Turner

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

43 citing papers in PubMed, 58 citations in OpenAlex.

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  15. Biophysics of Cell-Substrate Interactions Under Shear.Frontiers in cell and developmental biology · 2019
    Review
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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

3 authors at 2 institutions in 2 countries.

Nicholas O DeakinDepartment of Cell and Developmental Biology, State University of New York Upstate Medical University, Syracuse, New York, United States of America.
Christoph Ballestrem
Christopher E Turner
SUNY Upstate Medical University · USWellcome Centre for Cell-Matrix Research · GB

Funding

STRUCTURE AND FUNCTION OF PAXILLINR01GM047607 · NIGMS · UPSTATE MEDICAL UNIVERSITY · PI TURNER, CHRISTOPHER E · 1996 to 2017
$5.5M
ILK-Actopaxin Interactions in Cell SignalingR01HL070244 · NHLBI · UPSTATE MEDICAL UNIVERSITY · PI TURNER, CHRISTOPHER E · 2002 to 2010
$3.0M
NHLBI NIH HHS HL070244NHLBI NIH HHS R01 HL070244NIGMS NIH HHS R01 GM047607NIGMS NIH HHS R01 GM47607
6 · The paper itself

Abstract

Cell migration is of paramount importance to organism development and maintenance as well as multiple pathological processes, including cancer metastasis. The RhoGTPases Rac1 and RhoA are indispensable for cell migration as they regulate cell protrusion, cell-extracellular matrix (ECM) interactions and force transduction. However, the consequences of their activity at a molecular level within the cell remain undetermined. Using a combination of FRET, FRAP and biochemical analyses we show that the interactions between the focal adhesion proteins vinculin and paxillin, as well as the closely related family member Hic-5 are spatially and reciprocally regulated by the activity of Rac1 and RhoA. Vinculin in its active conformation interacts with either paxillin or Hic-5 in adhesions in response to Rac1 and RhoA activation respectively, while inactive vinculin interacts with paxillin in the membrane following Rac1 inhibition. Additionally, Rac1 specifically regulates the dynamics of paxillin as well as its binding partner and F-actin interacting protein actopaxin (α-parvin) in adhesions. Furthermore, FRET analysis of protein:protein interactions within cell adhesions formed in 3D matrices revealed that, in contrast to 2D systems vinculin interacts preferentially with Hic-5. This study provides new insight into the complexity of cell-ECM adhesions in both 2D and 3D matrices by providing the first description of RhoGTPase-coordinated protein:protein interactions in a cellular microenvironment. These data identify discrete roles for paxillin and Hic-5 in Rac1 and RhoA-dependent cell adhesion formation and maturation; processes essential for productive cell migration.

Indexed as

3T3 CellsAnimalsCell AdhesionCell MovementCells, CulturedCytoskeletal ProteinsDNA-Binding ProteinsFocal AdhesionsLIM Domain ProteinsMicePaxillinrac1 GTP-Binding ProteinrhoA GTP-Binding ProteinSignal TransductionVinculinCytoskeletal ProteinsDNA-Binding ProteinsLIM Domain ProteinsPaxillinrac1 GTP-Binding ProteinrhoA GTP-Binding ProteinTgfb1i1 protein, mouseVinculin

Identifiers

PMID22629471
PMCPMC3358283
OpenAlexW2045474213

What OpenQuestion holds

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LicenceCC BY
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.