Evidence map›Paper›PMID 30254327›Full record

ArticleScientific reports2018

Medium throughput breathing human primary cell alveolus-on-chip model.

Janick D Stucki, Nina Hobi, Artur Galimov, Andreas O Stucki, Nicole Schneider-Daum, Claus-Michael Lehr, Hanno Huwer, Manfred Frick, Manuela Funke-Chambour, Thomas Geiser and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 1 pooled it
8.2field-weighted citation impact, top 2% 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

78 citing papers in PubMed, 1 synthesis or guideline pooled it, 180 citations in OpenAlex.

  1. Advances in Engineering Human Tissue Models.Frontiers in bioengineering and biotechnology · 2020
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18 more citing papers are in PubMed but not listed here.

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

11 authors at 4 institutions in 3 countries.

Janick D StuckiARTORG Center for Biomedical Engineering Research, Organs-on-Chip Technologies, University of Bern, Bern, Switzerland.
Nina HobiARTORG Center for Biomedical Engineering Research, Organs-on-Chip Technologies, University of Bern, Bern, Switzerland.
Artur GalimovARTORG Center for Biomedical Engineering Research, Organs-on-Chip Technologies, University of Bern, Bern, Switzerland.
Andreas O StuckiARTORG Center for Biomedical Engineering Research, Organs-on-Chip Technologies, University of Bern, Bern, Switzerland.
Nicole Schneider-DaumHelmholtz Institute for Pharmaceutical Research Saarland, Helmholtz Center for Infection Research, Biopharmaceutics and Pharmaceutical Technology, Saarland University, Saarbrücken, Germany.
Claus-Michael LehrHelmholtz Institute for Pharmaceutical Research Saarland, Helmholtz Center for Infection Research, Biopharmaceutics and Pharmaceutical Technology, Saarland University, Saarbrücken, Germany.
Hanno HuwerSHG Clinics, Department of Cardiothoracic Surgery, Völklingen Heart Center, Völklingen, Germany.
Manfred FrickInstitute of General Physiology, University of Ulm, Ulm, Germany.ORCID 0000-0002-4763-1104
Manuela Funke-ChambourDepartment of Pulmonary Medicine, University Hospital of Bern, Bern, Switzerland.
Thomas GeiserDepartment of Pulmonary Medicine, University Hospital of Bern, Bern, Switzerland.
Olivier T GuenatARTORG Center for Biomedical Engineering Research, Organs-on-Chip Technologies, University of Bern, Bern, Switzerland. olivier.guenat@artorg.unibe.ch.ORCID 0000-0003-1103-9712
University of Bern · CHHelmholtz Institute for Pharmaceutical Research Saarland · DEKnappschaftskrankenhaus Recklinghausen · DEUniversität Ulm · DE

Funding

Carl-Zeiss-Stiftung (Carl Zeiss Foundation) D.4737Stiftung Forschung 3R (3R Research Foundation Switzerland) 143-15
6 · The paper itself

Abstract

Organs-on-chips have the potential to improve drug development efficiency and decrease the need for animal testing. For the successful integration of these devices in research and industry, they must reproduce in vivo contexts as closely as possible and be easy to use. Here, we describe a 'breathing' lung-on-chip array equipped with a passive medium exchange mechanism that provide an in vivo-like environment to primary human lung alveolar cells (hAEpCs) and primary lung endothelial cells. This configuration allows the preservation of the phenotype and the function of hAEpCs for several days, the conservation of the epithelial barrier functionality, while enabling simple sampling of the supernatant from the basal chamber. In addition, the chip design increases experimental throughput and enables trans-epithelial electrical resistance measurements using standard equipment. Biological validation revealed that human primary alveolar type I (ATI) and type II-like (ATII) epithelial cells could be successfully cultured on the chip over multiple days. Moreover, the effect of the physiological cyclic strain showed that the epithelial barrier permeability was significantly affected. Long-term co-culture of primary human lung epithelial and endothelial cells demonstrated the potential of the lung-on-chip array for reproducible cell culture under physiological conditions. Thus, this breathing lung-on-chip array, in combination with patients' primary ATI, ATII, and lung endothelial cells, has the potential to become a valuable tool for lung research, drug discovery and precision medicine.

Indexed as

RespirationEpithelial CellsEquipment DesignHumansPulmonary AlveoliReproducibility of ResultsTissue Array Analysis

Identifiers

PMID30254327
PMCPMC6156575
OpenAlexW2891868922

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.