Evidence map›Paper›PMID 23884246›Full record

ArticleThe Journal of investigative dermatology2014

Plakophilin 2 affects cell migration by modulating focal adhesion dynamics and integrin protein expression.

Jennifer L Koetsier, Evangeline V Amargo, Viktor Todorović, Kathleen J Green, Lisa M Godsel

Abstract read
In one paragraph

Article in The Journal of investigative dermatology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

20 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
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  12. Article
  13. Article
  14. Review
  15. Article
  16. Desmosome regulation and signaling in disease.Cell and tissue research · 2015
    Review
  17. Article
  18. Characterization of partially lifted cell sheets.Tissue engineering. Part A · 2014
    Article
  19. Review
  20. Review
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

5 authors at 1 institution in 1 country.

Jennifer L KoetsierDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Evangeline V AmargoDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Viktor TodorovićDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Kathleen J GreenDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA; Department of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Lisa M GodselDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA; Department of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA. Electronic address: l-godsel@northwestern.edu.
Northwestern University · US

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LEONIDAS C. PLATANIAS · 1993 to 2026
$153.9M
The Role of Keratinocytes as Independent ThermosensorsP30AR057216 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI PALLER, AMY S · 2009 to 2018
$6.0M
Desmoplakin Assembly and Function in EpidermisR37AR043380 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI GREEN, KATHLEEN JANEE · 2011 to 2020
$4.6M
Regulation of Desmosomal Cadherins in Oral CancerR01CA122151 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI GREEN, KATHLEEN JANEE · 2006 to 2016
$2.6M
Andor Revolution XD Live Cell Imaging System with Photomanipulation LaserS10RR031680 · NCRR · NORTHWESTERN UNIVERSITY AT CHICAGO · PI GELFAND, VLADIMIR I · 2011 to 2011
$437k
NCI NIH HHS P30 CA060553NCI NIH HHS R01 CA122151NCRR NIH HHS S10 RR031680NIAMS NIH HHS 1P30AR057216-01NIAMS NIH HHS P30 AR057216NIAMS NIH HHS R37 AR043380
6 · The paper itself

Abstract

Plakophilin 2 (PKP2), a desmosome component, modulates the activity and localization of the small GTPase RhoA at sites of cell-cell contact. PKP2 regulates cortical actin rearrangement during junction formation, and its loss is accompanied by an increase in actin stress fibers. We hypothesized that PKP2 may regulate focal adhesion dynamics and cell migration. Here we show that PKP2-deficient cells bind efficiently to the extracellular matrix, but upon spreading display total cell areas ≈ 30% smaller than control cells. Focal adhesions in PKP2-deficient cells are ≈ 2 × larger and more stable than in control cells, and vinculin displays an increased time for fluorescence recovery after photobleaching. Furthermore, β4 and β1 integrin protein and mRNA expression is elevated in PKP2-silenced cells. Normal focal adhesion phenotypes can be restored in PKP2-null cells by dampening the RhoA pathway or silencing β1 integrin. However, integrin expression levels are not restored by RhoA signaling inhibition. These data uncover a potential role for PKP2 upstream of β1 integrin and RhoA in integrating cell-cell and cell-substrate contact signaling in basal keratinocytes necessary for the morphogenesis, homeostasis, and reepithelialization of the stratified epidermis.

Indexed as

Cell LineCell MovementDesmosomesEpithelial CellsFocal AdhesionsHumansIntegrin beta1Integrin beta4KeratinocytesPlakophilinsrhoA GTP-Binding ProteinSignal TransductionWound HealingIntegrin beta1Integrin beta4PKP2 protein, humanPlakophilinsrhoA GTP-Binding ProteinRHOA protein, human

Identifiers

PMID23884246
PMCPMC4216696
OpenAlexW1991591829

What OpenQuestion holds

Textmetadata
LicenceTDM
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.