Evidence map›Paper›PMID 31409889›Full record

ArticleLaboratory investigation; a journal of technical methods and pathology2020

Mouse pancreatic ductal organoid culture as a relevant model to study exocrine pancreatic ion secretion.

Réka Molnár, Tamara Madácsy, Árpád Varga, Margit Németh, Xénia Katona, Marietta Görög, Brigitta Molnár, Júlia Fanczal, Zoltán Rakonczay, Péter Hegyi and 2 more

Open access · bronzeAbstract readEvaluation Study
PubMed Publisher
In one paragraph

Article in Laboratory investigation; a journal of technical methods and pathology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 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

12 authors at 1 institution in 1 country.

Réka MolnárFirst Department of Medicine, University of Szeged, Szeged, Hungary.ORCID http://orcid.org/0000-0002-3128-825X
Tamara MadácsyFirst Department of Medicine, University of Szeged, Szeged, Hungary.
Árpád VargaFirst Department of Medicine, University of Szeged, Szeged, Hungary.ORCID http://orcid.org/0000-0002-2379-139X
Margit NémethFirst Department of Medicine, University of Szeged, Szeged, Hungary.
Xénia KatonaFirst Department of Medicine, University of Szeged, Szeged, Hungary.
Marietta GörögFirst Department of Medicine, University of Szeged, Szeged, Hungary.
Brigitta MolnárFirst Department of Medicine, University of Szeged, Szeged, Hungary.
Júlia FanczalFirst Department of Medicine, University of Szeged, Szeged, Hungary.
Zoltán RakonczayDepartment of Pathophysiology, University of Szeged, Szeged, Hungary.
Péter HegyiHAS-USZ Momentum Translational Gastroenterology Research Group, University of Szeged, Szeged, Hungary.
Petra PallagiFirst Department of Medicine, University of Szeged, Szeged, Hungary.
József MaléthFirst Department of Medicine, University of Szeged, Szeged, Hungary. maleth.jozsef@med.u-szeged-hu.ORCID http://orcid.org/0000-0001-5768-3090
University of Szeged · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic exocrine secretory processes are challenging to investigate on primary epithelial cells. Pancreatic organoid cultures may help to overcome shortcomings of the current models, however the ion secretory processes in pancreatic organoids-and therefore their physiological relevance or their utility in disease modeling-are not known. To answer these questions, we provide side-by-side comparison of gene expression, morphology, and function of epithelial cells in primary isolated pancreatic ducts and organoids. We used mouse pancreatic ductal fragments for experiments or were grown in Matrigel to obtain organoid cultures. Using PCR analysis we showed that gene expression of ion channels and transporters remarkably overlap in primary ductal cells and organoids. Morphological analysis with scanning electron microscopy revealed that pancreatic organoids form polarized monolayers with brush border on the apical membrane. Whereas the expression and localization of key proteins involved in ductal secretion (cystic fibrosis transmembrane conductance regulator, Na

Indexed as

OrganoidsAnimalsCalcium SignalingCulture TechniquesCystic Fibrosis Transmembrane Conductance RegulatorIonsMicePancreas, ExocrinePancreatic DuctsCftr protein, mouseCystic Fibrosis Transmembrane Conductance RegulatorIons

Identifiers

PMID31409889
OpenAlexW2967395171

What Socratic holds

Textmetadata
Read underepoch 390

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 Socratic graph.