Evidence map›Paper›PMID 12093868›Full record

ArticleThe Journal of experimental medicine2002

Proteolytic processing of Stat6 signaling in mast cells as a negative regulatory mechanism.

Kotaro Suzuki, Hiroshi Nakajima, Shin-Ichiro Kagami, Akira Suto, Kei Ikeda, Koichi Hirose, Takaki Hiwasa, Kiyoshi Takeda, Yasushi Saito, Shizuo Akira and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2002. 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
1.7field-weighted citation impact, top 16% 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, 47 citations in OpenAlex.

  1. Review
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  7. Solitary fibrous tumors: loss of chimeric protein expression and genomic instability mark dedifferentiation.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2015
    Article
  8. Article
  9. Calpain-1 contributes to IgE-mediated mast cell activation.Journal of immunology (Baltimore, Md. : 1950) · 2014
    Article
  10. Review
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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

11 authors at 2 institutions in 1 country.

Kotaro SuzukiDepartment of Internal Medicine II, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Hiroshi Nakajima
Shin-Ichiro Kagami
Akira Suto
Kei Ikeda
Koichi Hirose
Takaki Hiwasa
Kiyoshi Takeda
Yasushi Saito
Shizuo Akira
Itsuo Iwamoto
Chiba University · JPThe University of Osaka · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accumulating evidence has shown the importance of Stat6-mediated signaling in allergic diseases. In this study, we show a novel regulatory mechanism of Stat6-mediated signaling in mast cells. When Stat6 is activated by interleukin (IL)-4 and translocated to the nucleus, Stat6 is cleaved by a nucleus-associated protease in mast cells. The cleaved 65-kD Stat6 lacks the COOH-terminal transactivation domain and functions as a dominant-negative molecule to Stat6-mediated transcription. The retrovirus-mediated expression of cleavage-resistant Stat6 mutants prolongs the nuclear accumulation of Stat6 upon IL-4 stimulation and enhances IL-4-induced gene expression and growth inhibition in mast cells. These results indicate that the proteolytic processing of Stat6 functions as a lineage-specific negative regulator of Stat6-dependent signaling in mast cells, and thus suggest that it may account for the limited role of Stat6 in IL-4 signaling in mast cells.

Indexed as

Milk ProteinsAnimalsApoptosisCell DivisionCell NucleusCells, CulturedCOS CellsDNA-Binding ProteinsFeedback, PhysiologicalGenes, DominantInterleukin-4Mast CellsMiceMice, Inbred C57BLMice, KnockoutMutagenesis, Site-DirectedDNA-Binding ProteinsInterleukin-4Milk ProteinsProtein IsoformsReceptors, IgESerine EndopeptidasesSerine Proteinase InhibitorsSTAT5 Transcription FactorStat6 protein, mouseSTAT6 Transcription FactorTrans-Activators

Identifiers

PMID12093868
PMCPMC2194019
OpenAlexW2105803506

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.