Evidence map›Paper›PMID 24043783›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

Actin-related protein2/3 complex regulates tight junctions and terminal differentiation to promote epidermal barrier formation.

Kang Zhou, Andrew Muroyama, Julie Underwood, Rebecca Leylek, Samriddha Ray, Scott H Soderling, Terry Lechler

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
3.9field-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

51 citing papers in PubMed, 80 citations in OpenAlex.

  1. Article
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  4. Article
  5. YAP/TAZ Signalling Controls Epidermal Keratinocyte Fate.International journal of molecular sciences · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Functions of Arp2/3 Complex in the Dynamics of Epithelial Tissues.Frontiers in cell and developmental biology · 2022
    Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. 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

7 authors at 2 institutions in 2 countries.

Kang ZhouDepartments of Cell Biology, Neurobiology, and Dermatology, Duke University Medical Center, Durham, NC 27710.
Andrew Muroyama
Julie Underwood
Rebecca Leylek
Samriddha Ray
Scott H Soderling
Terry Lechler
Duke Medical Center · USInstitute of Neurobiology · BG

Funding

ORGANIZATION AND FUNCTIONS OF CELLULAR STRUCTUREST32GM007184 · NIGMS · DUKE UNIVERSITY · PI JINKS-ROBERTSON, SUE · 1985 to 2019
$18.2M
Role of Cell Adhesion and the Cytoskeleton in Epidermal IntegrityR01AR055926 · NIAMS · DUKE UNIVERSITY · PI LECHLER, TERRY H · 2009 to 2019
$3.7M
GAPs in Signaling to the Spine and Retardation: Mechanisms and the Role of WRPR01NS059957 · NINDS · DUKE UNIVERSITY · PI SODERLING, SCOTT H · 2008 to 2017
$3.1M
NIAMS NIH HHS R01 AR055926NIAMS NIH HHS R01-AR055926NIGMS NIH HHS T32 GM007184NINDS NIH HHS R01 NS059957NINDS NIH HHS R01-NS059957
6 · The paper itself

Abstract

The epidermis provides an essential seal from the external environment and retains fluids within the body. To form an effective barrier, cells in the epidermis must form tight junctions and terminally differentiate into cornified envelopes. Here, we demonstrate that the branched actin nucleator, the actin-related protein (Arp)2/3 complex, is unexpectedly required for both these activities. Loss of the ArpC3 subunit of the Arp2/3 complex resulted in minimal changes in the morphogenesis and architecture of this stratified squamous epithelium, but resulted in profound defects in its physiology. Mutant embryos did not develop an effective barrier to the external environment and died within hours of birth. We discovered two underlying causes for these effects. First, ArpC3 was essential for robust assembly and function of tight junctions, specialized cell-cell adhesions that restrict water loss in the epidermis. Second, there were defects in differentiation of the epidermis and the production of cornified envelopes, structures essential for barrier activity. Underlying this defect, we found that YAP was inappropriately active not only in the ArpC3 mutant tissue, but also in cultured cells. Inhibition of YAP activity rescued the differentiation and barrier defects caused by loss of ArpC3. These results demonstrate previously unappreciated roles for the Arp2/3 complex and highlight the functions of branched actin networks in a complex tissue.

Indexed as

Actin-Related Protein 2Actin-Related Protein 3ActinsAdaptor Proteins, Signal TransducingAnimalsBenzothiazolesCell Cycle ProteinsDiaminesEpidermisFluorescence Recovery After PhotobleachingIndolesKeratinocytesListeria monocytogenesMiceMicroarray AnalysisMultiprotein ComplexesActin-Related Protein 2Actin-Related Protein 3ActinsAdaptor Proteins, Signal TransducingBenzothiazolesCell Cycle ProteinsCK-0944636DiaminesIndolesMultiprotein ComplexesOrganic ChemicalsPhosphoproteinsQuinolinesSYBR Green IThiophenesYap1 protein, mouseYAP-Signaling Proteins

Identifiers

PMID24043783
PMCPMC3791730
OpenAlexW1987356191

What OpenQuestion holds

Textmetadata
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.