Evidence map›Paper›PMID 29523846›Full record

ArticleScientific reports2018

NF-κB is weakly activated in the NOD mouse model of type 1 diabetes.

Allison E Irvin, Gaurang Jhala, Yuxing Zhao, Timothy S Blackwell, Balasubramanian Krishnamurthy, Helen E Thomas, Thomas W H Kay

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
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  9. Regulation and Mechanism of miR-518d through the PPARJournal of diabetes research · 2020
    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.

Allison E IrvinImmunology and Diabetes Unit, St Vincent's Institute, Fitzroy, Victoria, Australia.
Gaurang JhalaImmunology and Diabetes Unit, St Vincent's Institute, Fitzroy, Victoria, Australia.
Yuxing ZhaoImmunology and Diabetes Unit, St Vincent's Institute, Fitzroy, Victoria, Australia.
Timothy S BlackwellDepartments of Medicine and Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, TN, 37232, USA.
Balasubramanian KrishnamurthyImmunology and Diabetes Unit, St Vincent's Institute, Fitzroy, Victoria, Australia.
Helen E ThomasImmunology and Diabetes Unit, St Vincent's Institute, Fitzroy, Victoria, Australia. hthomas@svi.edu.au.
Thomas W H KayImmunology and Diabetes Unit, St Vincent's Institute, Fitzroy, Victoria, Australia.
St Vincents Institute of Medical Research · AUVanderbilt University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type 1 diabetes is an autoimmune disease characterised by selective destruction of pancreatic beta cells by the immune system. The transcription factor nuclear factor-kappa B (NF-κB) regulates innate and adaptive immune responses. Using gene targeting and in vitro analysis of pancreatic islets and immune cells, NF-κB activation has been implicated in type 1 diabetes development. Here we use a non-obese diabetic (NOD) mouse model that expresses a luciferase reporter of transcriptionally active NF-κB to determine its activation in vivo during development of diabetes. Increased luciferase activity was readily detected upon treatment with Toll-like receptor ligands in vitro and in vivo, indicating activation of NF-κB. However, activated NF-κB was detectable at low levels above background in unmanipulated NOD mice, but did not vary with age, despite the progression of inflammatory infiltration in islets over time. NF-κB was highly activated in an accelerated model of type 1 diabetes that requires CD4

Indexed as

AnimalsDendritic CellsDiabetes Mellitus, Type 1Disease Models, AnimalMacrophagesMiceMice, Inbred NODNF-kappa BTranscription, GeneticNF-kappa B

Identifiers

PMID29523846
PMCPMC5844878
OpenAlexW2798075812

What OpenQuestion holds

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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.