Evidence map›Paper›PMID 15867147›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2005

Disruption of the Jnk2 (Mapk9) gene reduces destructive insulitis and diabetes in a mouse model of type I diabetes.

Anja Jaeschke, Mercedes Rincón, Beth Doran, Judith Reilly, Donna Neuberg, Dale L Greiner, Leonard D Shultz, Aldo A Rossini, Richard A Flavell, Roger J Davis

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

34 citing papers in PubMed, 94 citations in OpenAlex.

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  9. The role of stress kinases in metabolic disease.Nature reviews. Endocrinology · 2020
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  15. Specific splice variants are associated with Parkinson's disease.Movement disorders : official journal of the Movement Disorder Society · 2013
    Article
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  17. 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

10 authors at 1 institution in 1 country.

Anja JaeschkeHoward Hughes Medical Institute and Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Mercedes Rincón
Beth Doran
Judith Reilly
Donna Neuberg
Dale L Greiner
Leonard D Shultz
Aldo A Rossini
Richard A Flavell
Roger J Davis
University of Massachusetts Chan Medical School · US

Funding

INTERCELLULAR SIGNALS AND INTESTINAL AGANGLIONOSISR01DK052530 · NIDDK · UNIVERSITY OF WASHINGTON · PI KAPUR, RAJ P. · 1997 to 2000
$241k
NIDDK NIH HHS DK52530
6 · The paper itself

Abstract

The c-Jun NH(2)-terminal kinase isoform (JNK) 1 is implicated in type 2 diabetes. However, a potential role for the JNK2 protein kinase in diabetes has not been established. Here, we demonstrate that JNK2 may play an important role in type 1 (insulin-dependent) diabetes that is caused by autoimmune destruction of beta cells. Studies of nonobese diabetic mice demonstrated that disruption of the Mapk9 gene (which encodes the JNK2 protein kinase) decreased destructive insulitis and reduced disease progression to diabetes. CD4(+) T cells from JNK2-deficient nonobese diabetic mice produced less IFN-gamma but significantly increased amounts of IL-4 and IL-5, indicating polarization toward the Th2 phenotype. This role of JNK2 to control the Th1/Th2 balance of the immune response represents a mechanism of protection against autoimmune diabetes. We conclude that JNK protein kinases may have important roles in diabetes, including functions of JNK1 in type 2 diabetes and JNK2 in type 1 diabetes.

Indexed as

Gene Expression RegulationAnimalsApoptosisCD4-Positive T-LymphocytesCell DifferentiationDiabetes Mellitus, ExperimentalFemaleImmune SystemImmunohistochemistryInsulinMaleMiceMice, Inbred NODMice, SCIDMice, TransgenicMicroscopy, FluorescenceInsulinMitogen-Activated Protein Kinase 9Protein Isoforms

Identifiers

PMID15867147
PMCPMC1100789
OpenAlexW1990898321

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.