Evidence map›Paper›PMID 24391943›Full record

ArticlePloS one2013

Generation of a new congenic mouse strain with enhanced chymase expression in mast cells.

Xi Jin, Wanke Zhao, Kaiyao Shi, Wanting T Ho, Zhizhuang J Zhao

Open access · goldAbstract 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 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

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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

5 authors at 1 institution in 2 countries.

Xi JinDepartment of Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, United States of America.
Wanke ZhaoDepartment of Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, United States of America.
Kaiyao ShiDepartment of Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, United States of America ; Department of Cardiology, China-Japan Union Hospital of Jilin University, Changchun, China.
Wanting T HoDepartment of Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, United States of America.
Zhizhuang J ZhaoDepartment of Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, United States of America.
University of Oklahoma Health Sciences Center · US

Funding

Tyrosine Phosphatases PTP-MEG2 and HematopoiesisR01HL079441 · NHLBI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI ZHAO, ZHIZHUANG JOE · 2006 to 2009
$1.4M
Tyrosine Phosphatase in Signal TransductionR01HL076309 · NHLBI · VANDERBILT UNIVERSITY · PI ZHAO, ZHIZHUANG JOE · 2004 to 2007
$1.3M
NHLBI NIH HHS HL076309NHLBI NIH HHS HL079441NHLBI NIH HHS R01 HL076309NHLBI NIH HHS R01 HL079441
6 · The paper itself

Abstract

Mast cells are effector cells best known for their roles in IgE-associated allergy, but they also play a protective role in defense against pathogens. These cells express high levels of proteases including chymase, tryptase and carboxypeptidase. In the present study, we identified a congenic strain of C57BL/6 mice expressing an extraordinarily high level of chymases Mcp-2 and Mcp-4 in mast cells. The overexpression was associated with variant Mcp-2 and Mcp-4 genes originated from DBA/2 mice that also expressed high levels of the two enzymes. Real time PCR analysis revealed that Mcp-2 and Mcp-4 were selectively overexpressed as tryptases, Cpa3 and several other chymases were kept at normal levels. Reporter gene assays demonstrated that single-nucleotide polymorphisms (SNPs) in the promoter region of Mcp-2 gene may be partly responsible for the increased gene transcription. Our study provides a new model system to study the function of mast cell chymases. The data also suggest that expression of chymases differs considerably in different strains of mice and the increased chymase activity may be responsible for some unique phenotypes observed in DBA/2 mice.

Indexed as

Models, AnimalAnimalsBlotting, WesternChymasesCloning, MolecularDNA PrimersFluorescent Antibody TechniqueMast CellsMiceMice, CongenicMice, Inbred C57BLProteomicsReal-Time Polymerase Chain ReactionSerine Endopeptidaseschymase 2ChymasesDNA Primersmast cell protease 4Serine Endopeptidases

Identifiers

PMID24391943
PMCPMC3877308
OpenAlexW2072960648

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.