Evidence map›Paper›PMID 40735520›Full record

ArticleMethodsX2025

Differentiation and histological analysis of primary human bronchial epithelial cells cultured on transwell membranes using air-liquid interface culture.

Asha Ashraf, Erica D Bruce

Abstract read
In one paragraph

Article in MethodsX, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

2 authors.

Asha AshrafDepartment of Environmental Science, Baylor University, 101 Bagby Ave., Waco, TX, 76706, USA.
Erica D BruceDepartment of Environmental Science, Baylor University, 101 Bagby Ave., Waco, TX, 76706, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This protocol describes a reproducible and optimized workflow for the differentiation and histological analysis of primary normal human bronchial epithelial cells (NHBECs) cultured on Transwell membranes using air-liquid interface (ALI) culture. The method begins with expansion of early-passage NHBECs under submerged conditions, followed by seeding on collagen-coated Transwell inserts. Upon reaching confluence, cells are transitioned to ALI conditions using PneumaCult™-ALI maintenance medium for 21-28 days, promoting mucociliary differentiation. After differentiation, membranes are fixed, cryoprotected in graded sucrose solutions, embedded in Optimal Cutting Temperature (OCT) compound, and then cryosectioned. Sections are subsequently stained using hematoxylin and eosin (H&E) to assess epithelial morphology, or periodic acid-Schiff (PAS) staining to visualize polysaccharide-containing structures such as mucins. This protocol supports the detailed structural and histological evaluation of NHBEC differentiation on a Transwell model, which is valuable for studies of airway epithelial biology, mucociliary function, and inhalation toxicology.•ALI differentiation of NHBECs on collagen-coated Transwell inserts.•Fixation, sucrose cryoprotection, and OCT embedding for cryosectioning.•H&E and PAS staining for visualization of epithelial cells and mucin.

Indexed as

Air-liquid interface cultureCell differentiationCryosectioningHistologyPrimary cell cultureRespiratory toxicology

Identifiers

PMID40735520
PMCPMC12304693

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.