Evidence map›Paper›PMID 12221138›Full record

ArticleMolecular biology of the cell2002

Purification and identification of secernin, a novel cytosolic protein that regulates exocytosis in mast cells.

Gemma Way, Nicholas Morrice, Carl Smythe, Antony J O'Sullivan

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

26 citing papers in PubMed, 46 citations in OpenAlex.

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  11. The Sertoli cell expressed gene secernin-1 (Scrn1) is dispensable for male fertility in the mouse.Developmental dynamics : an official publication of the American Association of Anatomists · 2021
    Article
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  13. In vitro and bioinformatics mechanistic-based approach for cadmium carcinogenicity understanding.Toxicology in vitro : an international journal published in association with BIBRA · 2020
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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

4 authors at 2 institutions in 1 country.

Gemma WayDepartment of Biological and Biomedical Sciences, University of Durham, United Kingdom.
Nicholas Morrice
Carl Smythe
Antony J O'Sullivan
Durham University · GBUniversity of Dundee · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

After permeabilization with the pore-forming toxin streptolysin-O mast cells can be triggered to secrete by addition of both calcium and a GTP analogue. If stimulation is delayed after permeabilization, there is a progressive decrease in the extent of secretion upon stimulation, eventually leading to a complete loss of the secretory response. This loss of secretory response can be retarded by the addition of cytosol from other secretory tissues, demonstrating that the response is dependent on a number of cytosolic proteins. We have used this as the basis of a bioassay to purify Secernin 1, a novel 50-kDa cytosolic protein that appears to be involved in the regulation of exocytosis from peritoneal mast cells. Secernin 1 increases both the extent of secretion and increases the sensitivity of mast cells to stimulation with calcium.

Indexed as

Amino Acid SequenceAnimalsCalciumCattleChromatographyChromatography, GelCytosolDose-Response Relationship, DrugDurapatiteExocytosisGlutathione TransferaseHumansMaleMass SpectrometryMast CellsMolecular Sequence DataCalciumDurapatiteGlutathione TransferaseNerve Tissue Proteinsphenyl-superoseProteinsRecombinant Fusion ProteinsSCRN1 protein, humansecernin 1 protein, mouseSepharoseSuperose 12

Identifiers

PMID12221138
PMCPMC124164
OpenAlexW2105611633

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.