Evidence map›Paper›PMID 24098462›Full record

ArticlePloS one2013

The jagged-2/notch-1/hes-1 pathway is involved in intestinal epithelium regeneration after intestinal ischemia-reperfusion injury.

Guoqing Chen, Yuan Qiu, Lihua Sun, Min Yu, Wensheng Wang, Weidong Xiao, Yang Yang, Yong Liu, Songwei Yang, Daniel H Teitelbaum and 3 more

Abstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

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  12. Coexpression of c-Met and Notch-1 correlates with poor prognosis in resected non-small-cell lung cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    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

13 authors.

Guoqing ChenDepartment of General Surgery, Xinqiao Hospital, Third Military Medical University, Chongqing, China.
Yuan Qiu
Lihua Sun
Min Yu
Wensheng Wang
Weidong Xiao
Yang Yang
Yong Liu
Songwei Yang
Daniel H Teitelbaum
Yuanhang Ma
Dingsong Lu
Hua Yang

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNotch signaling plays a critical role in the maintenance of intestinal crypt epithelial cell proliferation. The aim of this study was to investigate the role of Notch signaling in the proliferation and regeneration of intestinal epithelium after intestinal ischemia reperfusion (I/R) injury.

methodsMale Sprague-Dawley rats were subjected to sham operation or I/R by occlusion of the superior mesenteric artery (SMA) for 20 min. Intestinal tissue samples were collected at 0, 1, 2, 4, and 6 h after reperfusion. Proliferation of the intestinal epithelium was evaluated by immunohistochemical staining of proliferating nuclear antigen (PCNA). The mRNA and protein expression levels of Notch signaling components were examined using Real-time PCR and Western blot analyses. Immunofluorescence was also performed to detect the expression and location of Jagged-2, cleaved Notch-1, and Hes-1 in the intestine. Finally, the γ-secretase inhibitor DAPT and the siRNA for Jagged-2 and Hes-1 were applied to investigate the functional role of Notch signaling in the proliferation of intestinal epithelial cells in an in vitro IEC-6 culture system.

resultsI/R injury caused increased intestinal crypt epithelial cell proliferation and increased mRNA and protein expression of Jagged-2, Notch-1, and Hes-1. The immunofluorescence results further confirmed increased protein expression of Jagged-2, cleaved Notch-1, and Hes-1 in the intestinal crypts. The inhibition of Notch signaling with DAPT and the suppression of Jagged-2 and Hes-1 expression using siRNA both significantly inhibited the proliferation of IEC-6 cells.

conclusionThe Jagged-2/Notch-1/Hes-1 signaling pathway is involved in intestinal epithelium regeneration early after I/R injury by increasing crypt epithelial cell proliferation.

Indexed as

RegenerationSignal TransductionAnimalsBasic Helix-Loop-Helix ProteinsCell LineCell ProliferationDipeptidesDisease Models, AnimalGene SilencingHomeodomain ProteinsIntestinal MucosaJagged-2 ProteinMaleMembrane ProteinsProliferating Cell Nuclear AntigenRatsBasic Helix-Loop-Helix ProteinsDipeptidesHes1 protein, ratHomeodomain ProteinsJag2 protein, ratJagged-2 ProteinMembrane ProteinsN-(N-(3,5-difluorophenacetyl)alanyl)phenylglycine tert-butyl esterProliferating Cell Nuclear AntigenReceptor, Notch1Transcription Factor HES-1

Identifiers

PMID24098462
PMCPMC3789708

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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.