Evidence map›Paper›PMID 41441189›Full record

ArticleMethods and protocols2025

Optimized Whole-Mount Fluorescence Staining Protocol for Pulmonary Toxicity Evaluation Using Mouse Respiratory Epithelia.

Richard Francis

Abstract read
In one paragraph

Article in Methods and protocols, 2025. 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

1 author.

Richard FrancisCilia Research Laboratory, College of Medicine and Dentistry, James Cook University, Townsville, QLD 4814, Australia.ORCID 0000-0002-4401-1946

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A straightforward whole-mount approach has been developed that uses fluorescence imaging, mouse trachea, and a range of off-the-shelf reagents for rapidly evaluating substance toxicity within the ciliated respiratory epithelium. Using this protocol, the lumen of control trachea samples displays a typical cobblestone epithelial structure, a high density of ciliated cells, and minimal evidence of cell death, as visualized by phalloidin, acetylated tubulin, and fixable live/dead staining, respectively. In contrast, trachea subjected to treatments that induce injury show disrupted epithelial architecture and increased cell death, indicating substance toxicity. These results support the utility of this protocol for rapidly detecting and quantifying respiratory epithelial toxicity and differential cell-type susceptibility.

Indexed as

ciliated airway epitheliafluorescence microscopyimmunohistochemistry

Identifiers

PMID41441189
PMCPMC12736217

What OpenQuestion holds

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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.