Evidence map›Paper›PMID 11936755›Full record

ArticleInflammation2002

A new assay to monitor the degranulation process in phagocytizing human neutrophils.

Violetta Borelli, Maria Giovanna Perrotta, Francesca Vita, Maria Rosa Soranzo, Giuliano Zabucchi

Abstract read
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In one paragraph

Article in Inflammation, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Violetta BorelliDipartimento di Fisiologia e Patologia, Università di Trieste, Italy.
Maria Giovanna Perrotta
Francesca Vita
Maria Rosa Soranzo
Giuliano Zabucchi

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

oxidation, we set up a method for measuring MPO intraphagosomal release in human neutrophils. The method is based on the passive engulfment of DAB together with the phagocytosable particle. Inside the vacuole, this substrate is oxidized by MPO released from the azurophilic granules. The colorimetrical evaluation of the amount of DAB oxidized allows for cheap, rapid quantification of MPO intraphagosomal secretion in whole cells. Using this method, we show that the degranulation process, involving azurophilic granules, can be monitored carefully during phagocytosis. It takes place after the ingestion of zymosan particles opsonized with normal human serum, as well as during IgG-mediated phagocytosis and under conditions where beta2 integrins are blocked. However our findings also show that the extent of intraphagosomal secretion depends on either the extent of opsonization or the type of receptor engaged during the phagocytic event.

Indexed as

Cell DegranulationPhagocytosis3,3'-DiaminobenzidineChromogenic CompoundsColorimetryCytological TechniquesHumansKineticsNeutrophilsPeroxidaseReceptors, ImmunologicZymosan3,3'-DiaminobenzidineChromogenic CompoundsPeroxidasephagocytosis receptorReceptors, ImmunologicZymosan

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What OpenQuestion holds

Textmetadata
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Registered trials

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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.