Evidence map›Paper›PMID 21264230›Full record

ArticlePloS one2011

IκB kinase β regulates epithelium migration during corneal wound healing.

Liang Chen, Qinghang Meng, Winston Kao, Ying Xia

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

19 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  5. Effects of mannose-binding lectin on pulmonary gene expression and innate immune inflammatory response to ozone.American journal of physiology. Lung cellular and molecular physiology · 2016
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  9. IKK phosphorylates RelB to modulate its promoter specificity and promote fibroblast migration downstream of TNF receptors.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
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  16. Accelerated In Vitro Degradation of Optically Clear LowTranslational vision science & technology · 2013
    Article
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  18. 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

4 authors at 2 institutions in 1 country.

Liang ChenDepartment of Environmental Health, University of Cincinnati Medical Center, Cincinnati, Ohio, United States of America.
Qinghang Meng
Winston Kao
Ying Xia
University of Cincinnati · USUniversity of Cincinnati Medical Center · US

Funding

The Role of MAP 3 Kinase 1 in Ocular Surface MorphogenesisR01EY015227 · NEI · UNIVERSITY OF CINCINNATI · PI XIA, YING · 2004 to 2019
$5.4M
NEI NIH HHS EY 15227NEI NIH HHS R01 EY015227
6 · The paper itself

Abstract

The IKKβ is known to regulate transcription factor NF-κB activation leading to inflammatory responses. Recent gene knockout studies have shown that IKKβ can orchestrate local inflammatory responses and regulate homeostasis of epithelial tissues. To investigate whether IKKβ has an intrinsic role in epithelial cells, we established an in vivo system in the immune privileged corneal epithelium. We generated triple transgenic Krt12(rtTA/rtTAt)/tet-O-Cre/Ikkβ(F/F) (Ikkβ(ΔCE/ΔCE)) mice by crossing the Krt12-rtTA knock-in mice, which express the reverse tetracycline transcription activator in corneal epithelial cells, with the tet-O-Cre and Ikkβ(F/F) mice. Doxycycline-induced IKKβ ablation occurred in corneal epithelial cells of triple transgenic Ikkβ(ΔCE/ΔCE) mice, but loss of IKKβ did not cause ocular abnormalities in fetal development and postnatal maintenance. Instead, loss of IKKβ significantly delayed healing of corneal epithelial debridement without affecting cell proliferation, apoptosis or macrophage infiltration. In vitro studies with human corneal epithelial cells (HCEpi) also showed that IKKβ was required for cytokine-induced cell migration and wound closure but was dispensable for cell proliferation. In both in vivo and in vitro settings, IKKβ was required for optimal activation of NF-κB and p38 signaling in corneal epithelial cells, and p38 activation is likely mediated through formation of an IKKβ-p38 protein complex. Thus, our studies in corneal epithelium reveal a previously un-recognized role for IKKβ in the control of epithelial cell motility and wound healing.

Indexed as

Cell MovementWound HealingAnimalsCell ProliferationCorneal InjuriesEpithelial CellsEpithelium, CornealI-kappa B KinaseMiceMice, TransgenicNF-kappa Bp38 Mitogen-Activated Protein KinasesI-kappa B KinaseNF-kappa Bp38 Mitogen-Activated Protein Kinases

Identifiers

PMID21264230
PMCPMC3022035
OpenAlexW1974273388

What OpenQuestion holds

Textmetadata
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.