Evidence map›Paper›PMID 26739591›Full record

ArticleBiological research2016

Can widely used cell type markers predict the suitability of immortalized or primary mammary epithelial cell models?

Edgar Corneille Ontsouka, Janique Sabina Bertschi, Xiao Huang, Michael Lüthi, Stefan Müller, Christiane Albrecht

Open access · goldAbstract read
In one paragraph

Article in Biological research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

6 citing papers in PubMed, 17 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

6 authors at 1 institution in 1 country.

Edgar Corneille OntsoukaFaculty of Medicine, Institute of Biochemistry and Molecular Medicine, University of Bern, Buehlstrasse 28, 3012, Bern, Switzerland. corneille.ontsouka@ibmm.unibe.ch.
Janique Sabina BertschiFaculty of Medicine, Institute of Biochemistry and Molecular Medicine, University of Bern, Buehlstrasse 28, 3012, Bern, Switzerland. janique.21@hotmail.com.
Xiao HuangFaculty of Medicine, Institute of Biochemistry and Molecular Medicine, University of Bern, Buehlstrasse 28, 3012, Bern, Switzerland. xiao.huang@ibmm.unibe.ch.
Michael LüthiFaculty of Medicine, Institute of Biochemistry and Molecular Medicine, University of Bern, Buehlstrasse 28, 3012, Bern, Switzerland. michael.luethi@ibmm.unibe.ch.
Stefan MüllerDepartment of Clinical Research, Faculty of Medicine, University of Bern, 3010, Bern, Switzerland. stefan.mueller@dkf.unibe.ch.
Christiane AlbrechtFaculty of Medicine, Institute of Biochemistry and Molecular Medicine, University of Bern, Buehlstrasse 28, 3012, Bern, Switzerland. christiane.albrecht@ibmm.unibe.ch.
University of Bern · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMammary cell cultures are convenient tools for in vitro studies of mammary gland biology. However, the heterogeneity of mammary cell types, e.g., glandular milk secretory epithelial or myoepithelial cells, often complicates the interpretation of cell-based data. The present study was undertaken to determine the relevance of bovine primary mammary epithelial cells isolated from American Holstein (bMECUS) or Swiss Holstein-Friesian (bMECCH) cows, and of primary bovine mammary alveolar epithelial cells stably transfected with simian virus-40 (SV-40) large T-antigen (MAC-T) for in vitro analyses. This was evaluated by testing their expression pattern of cytokeratin (CK) 7, 18, 19, vimentin, and α-smooth muscle actin (α-SMA).

resultsThe expression of the listed markers was assessed using real-time quantitative PCR, flow cytometry and immunofluorescence microscopy. Characteristic markers of the mesenchymal (vimentin), myoepithelial (α-SMA) and glandular secretory cells (CKs) showed differential expression among the studied cell cultures, partly depending on the analytical method used. The relative mRNA expression of vimentin, CK7 and CK19, respectively, was lower (P < 0.05) in immortalized than in primary mammary cell cultures. The stain index (based on flow cytometry) of CK7 and CK19 protein was lower (P < 0.05) in MAC-T than in bMECs, while the expression of α-SMA and CK18 showed an inverse pattern. Immunofluorescence microscopy analysis mostly confirmed the mRNA data, while partly disagreed with flow cytometry data (e.g., vimentin level in MAC-T). The differential expression of CK7 and CK19 allowed discriminating between immortal and primary mammary cultures.

conclusionsThe expression of the selected widely used cell type markers in primary and immortalized MEC cells did not allow a clear preference between these two cell models for in vitro analyses studying aspects of milk composition. All tested cell models exhibited to a variable degree epithelial and mesenchymal features. Thus, based on their characterization with widely used cell markers, none of these cultures represent an unequivocal alveolar mammary epithelial cell model. For choosing the appropriate in vitro model additional properties such as the expression profile of specific proteins of interest (e.g., transporter proteins) should equally be taken into account.

Indexed as

ActinsAnalysis of VarianceAnimalsAntigens, Viral, TumorCattleCell LineCells, CulturedEpithelial CellsFemaleFlow CytometryKeratinsMammary Glands, AnimalMicroscopy, FluorescencePrimary Cell CultureReal-Time Polymerase Chain ReactionSimian virus 40ActinsAntigens, Viral, TumorKeratinsVimentin

Identifiers

PMID26739591
PMCPMC4702413
OpenAlexW2231179544

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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.