Evidence map›Paper›PMID 19955657›Full record

ArticleThe Journal of clinical investigation2010

Ablation of C/EBPbeta alleviates ER stress and pancreatic beta cell failure through the GRP78 chaperone in mice.

Tomokazu Matsuda, Yoshiaki Kido, Shun-ichiro Asahara, Tsuneyasu Kaisho, Takashi Tanaka, Naoko Hashimoto, Yutaka Shigeyama, Akihiko Takeda, Tae Inoue, Yuki Shibutani and 9 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

63 citing papers in PubMed, 112 citations in OpenAlex.

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3 more citing papers are in PubMed but not listed here.

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

19 authors at 6 institutions in 3 countries.

Tomokazu MatsudaDepartment of Internal Medicine, Division of Diabetes, Metabolism, and Endocrinology, Kobe University Graduate School of Medicine, Kobe, Japan.
Yoshiaki Kido
Shun-ichiro Asahara
Tsuneyasu Kaisho
Takashi Tanaka
Naoko Hashimoto
Yutaka Shigeyama
Akihiko Takeda
Tae Inoue
Yuki Shibutani
Maki Koyanagi
Tetsuya Hosooka
Michihiro Matsumoto
Hiroshi Inoue
Tohru Uchida
Masato Koike
Yasuo Uchiyama
Shizuo Akira
Masato Kasuga
Kobe University · JPOsaka University · JPSaitama International Medical Center · JPHarvard University · USKanazawa University · JPRMIT University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic beta cell failure is thought to underlie the progression from glucose intolerance to overt diabetes, and ER stress is implicated in such beta cell dysfunction. We have now shown that the transcription factor CCAAT/enhancer-binding protein beta (C/EBPbeta) accumulated in the islets of diabetic animal models as a result of ER stress before the onset of hyperglycemia. Transgenic overexpression of C/EBPbeta specifically in beta cells of mice reduced beta cell mass and lowered plasma insulin levels, resulting in the development of diabetes. Conversely, genetic ablation of C/EBPbeta in the beta cells of mouse models of diabetes, including Akita mice, which harbor a heterozygous mutation in Ins2 (Ins2WT/C96Y), and leptin receptor-deficient (Lepr-/-) mice, resulted in an increase in beta cell mass and ameliorated hyperglycemia. The accumulation of C/EBPbeta in pancreatic beta cells reduced the abundance of the molecular chaperone glucose-regulated protein of 78 kDa (GRP78) as a result of suppression of the transactivation activity of the transcription factor ATF6alpha, thereby increasing the vulnerability of these cells to excess ER stress. Our results thus indicate that the accumulation of C/EBPbeta in pancreatic beta cells contributes to beta cell failure in mice by enhancing susceptibility to ER stress.

Indexed as

Activating Transcription Factor 6AnimalsCCAAT-Enhancer-Binding Protein-betaEndoplasmic ReticulumEndoplasmic Reticulum Chaperone BiPHeat-Shock ProteinsInsulinInsulin-Secreting CellsInsulin SecretionMaleMembrane ProteinsMiceMice, Inbred C57BLPromoter Regions, GeneticReceptors, LeptinTrans-ActivatorsActivating Transcription Factor 6Atf6 protein, mouseCCAAT-Enhancer-Binding Protein-betaEndoplasmic Reticulum Chaperone BiPHeat-Shock ProteinsHspa5 protein, mouseInsulinleptin receptor, mouseMembrane ProteinsReceptors, LeptinTrans-Activators

Identifiers

PMID19955657
PMCPMC2798684
OpenAlexW1971825261

What Socratic 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 Socratic graph.