Evidence map›Paper›PMID 25610753›Full record

ArticleTissue barriers2014

Arp2/3 complex function in the epidermis.

Terry Lechler

Open access · hybridAbstract read
In one paragraph

Article in Tissue barriers, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Functions of Arp2/3 Complex in the Dynamics of Epithelial Tissues.Frontiers in cell and developmental biology · 2022
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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

1 author at 1 institution in 1 country.

Terry LechlerDepartments of Dermatology and Cell Biology, Duke University ; Durham, NC USA.
Duke University · US

Funding

Role of Cell Adhesion and the Cytoskeleton in Epidermal IntegrityR01AR055926 · NIAMS · DUKE UNIVERSITY · PI LECHLER, TERRY H · 2009 to 2019
$3.7M
NIAMS NIH HHS R01 AR055926
6 · The paper itself

Abstract

An exciting frontier in biology is understanding the functions of basic cell biological machinery in complex tissues. This approach is expected to uncover novel modes of regulation as well as reveal how core machinery is repurposed by different tissues to accomplish different physiological outputs. F-actin plays roles in cell shape, adhesion, migration and signaling - diverse functions that require a specific organization established by a myriad of regulators. Here, we discuss the role of the actin nucleating Arp2/3 complex and the unexpected roles that it plays in a stratified epithelial tissue, the epidermis. While many expected phenotypes such as defects in architecture and cell adhesion were lacking, loss of the Arp2/3 complex activity resulted in epidermal barrier and differentiation defects. This teaches us that, while informative, cell culture approaches are limiting and that studies of the Arp2/3 complex in diverse tissues are expected to yield many more surprises.

Indexed as

AJ, adherens junctionArp2/3 complexArp, Actin-related proteinEGFR, epidermal growth factor receptorepidermisFAK, focal adhesion kinaseFRAP, fluorescence recovery after photobleachingN-WASP, neural Wiskott-Aldrich synrome proteintight junctionYAP1ZO, zonula occludens

Identifiers

PMID25610753
PMCPMC4292041
OpenAlexW2040746533

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.