Evidence map›Paper›PMID 29267508›Full record

ArticleBrazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica2017

Characterization of air-liquid interface culture of A549 alveolar epithelial cells.

J Wu, Y Wang, G Liu, Y Jia, J Yang, J Shi, J Dong, J Wei, X Liu

Open access · goldAbstract read
In one paragraph

Article in Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

47 citing papers in PubMed, 114 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

9 authors at 3 institutions in 1 country.

J WuCollege of Clinical Medicine, Ningxia Medical University, Yinchuan, Ningxia, China.
Y WangCollege of Clinical Medicine, Ningxia Medical University, Yinchuan, Ningxia, China.
G LiuCollege of Clinical Medicine, Ningxia Medical University, Yinchuan, Ningxia, China.
Y JiaInstitute of Human Stem Cell Research, General Hospital of Ningxia Medical University, Yinchuan, Ningxia, China.
J YangInstitute of Human Stem Cell Research, General Hospital of Ningxia Medical University, Yinchuan, Ningxia, China.
J ShiInstitute of Human Stem Cell Research, General Hospital of Ningxia Medical University, Yinchuan, Ningxia, China.
J DongDepartment of Pathology, Ningxia Medical University, Yinchuan, Ningxia, China.
J WeiCollege of Clinical Medicine, Ningxia Medical University, Yinchuan, Ningxia, China.
X LiuCollege of Clinical Medicine, Ningxia Medical University, Yinchuan, Ningxia, China.
Ningxia Medical University · CNNingxia University · CNNingxia Medical University General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alveolar epithelia play an essential role in maintaining the integrity and homeostasis of lungs, in which alveolar epithelial type II cells (AECII) are a cell type with stem cell potential for epithelial injury repair and regeneration. However, mechanisms behind the physiological and pathological roles of alveolar epithelia in human lungs remain largely unknown, partially owing to the difficulty of isolation and culture of primary human AECII cells. In the present study, we aimed to characterize alveolar epithelia generated from A549 lung adenocarcinoma cells that were cultured in an air-liquid interface (ALI) state. Morphological analysis demonstrated that A549 cells could reconstitute epithelial layers in ALI cultures as evaluated by histochemistry staining and electronic microscopy. Immunofluorescent staining further revealed an expression of alveolar epithelial type I cell (AECI) markers aquaporin-5 protein (AQP-5), and AECII cell marker surfactant protein C (SPC) in subpopulations of ALI cultured cells. Importantly, molecular analysis further revealed the expression of AQP-5, SPC, thyroid transcription factor-1, zonula occludens-1 and Mucin 5B in A549 ALI cultures as determined by both immunoblotting and quantitative RT-PCR assay. These results suggest that the ALI culture of A549 cells can partially mimic the property of alveolar epithelia, which may be a feasible and alternative model for investigating roles and mechanisms of alveolar epithelia in vitro.

Indexed as

Culture Media, ConditionedA549 CellsAlveolar Epithelial CellsAnalysis of VarianceAquaporin 5Cell CountCell Culture TechniquesHumansImmunoblottingMicroscopy, Electron, ScanningMucin-5BPulmonary Surfactant-Associated Protein CReal-Time Polymerase Chain ReactionReference ValuesReproducibility of ResultsThyroid Nuclear Factor 1Aquaporin 5Culture Media, ConditionedMucin-5BNKX2-1 protein, humanPulmonary Surfactant-Associated Protein CThyroid Nuclear Factor 1Zonula Occludens-1 Protein

Identifiers

PMID29267508
PMCPMC5731333
OpenAlexW2772587132

What OpenQuestion holds

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LicenceCC BY
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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.