Evidence map›Paper›PMID 30653572›Full record

ArticlePloS one2019

Establishment of a pulmonary epithelial barrier on biodegradable poly-L-lactic-acid membranes.

Salvatore Montesanto, Natalie P Smithers, Fabio Bucchieri, Valerio Brucato, Vincenzo La Carrubba, Donna E Davies, Franco Conforti

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

7 authors at 4 institutions in 2 countries.

Salvatore MontesantoThe Brooke Laboratory, Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
Natalie P SmithersThe Brooke Laboratory, Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
Fabio BucchieriDepartment of Experimental Biomedicine and Clinical Neurosciences (BIONEC), University of Palermo, Palermo, Italy.
Valerio BrucatoDepartment of Civil, Environmental, Aerospace, Materials Engineering (DICAM), University of Palermo, Palermo, Italy.
Vincenzo La CarrubbaDepartment of Civil, Environmental, Aerospace, Materials Engineering (DICAM), University of Palermo, Palermo, Italy.
Donna E DaviesThe Brooke Laboratory, Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
Franco ConfortiThe Brooke Laboratory, Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.ORCID 0000-0001-5305-3155
Brooke · GBNational Interuniversity Consortium of Materials Science and Technology · ITUniversity Hospital Southampton NHS Foundation Trust · GBUniversity of Palermo · IT

Funding

Medical Research Council G0800766Medical Research Council G0900453MRF_ MRF-091-0003-RG-CONFO
6 · The paper itself

Abstract

Development of biocompatible and functional scaffolds for tissue engineering is a major challenge, especially for development of polarised epithelia that are critical structures in tissue homeostasis. Different in vitro models of the lung epithelial barrier have been characterized using non-degradable polyethylene terephthalate membranes which limits their uses for tissue engineering. Although poly-L-lactic acid (PLLA) membranes are biodegradable, those prepared via conventional Diffusion Induced Phase Separation (DIPS) lack open-porous geometry and show limited permeability compromising their use for epithelial barrier studies. Here we used PLLA membranes prepared via a modification of the standard DIPS protocol to control the membrane surface morphology and permeability. These were bonded to cell culture inserts for use in barrier function studies. Pulmonary epithelial cells (H441) readily attached to the PLLA membranes and formed a confluent cell layer within two days. This was accompanied by a significant increase in trans-epithelial electrical resistance and correlated with the formation of tight junctions and vectorial cytokine secretion in response to TNFα. Our data suggest that a structurally polarized and functional epithelial barrier can be established on PLLA membranes produced via a non-standard DIPS protocol. Therefore, PLLA membranes have potential utility in lung tissue engineering applications requiring bio-absorbable membranes.

Indexed as

Absorbable ImplantsBiocompatible MaterialsCell AdhesionCell Culture TechniquesCell LineCytokinesElectric ImpedanceEpithelial CellsHumansLungMaterials TestingMembranes, ArtificialPolyestersPolyethylene TerephthalatesTight JunctionsTissue EngineeringBiocompatible MaterialsCytokinesMembranes, ArtificialPolyestersPolyethylene Terephthalatespoly(lactide)

Identifiers

PMID30653572
PMCPMC6336298
OpenAlexW2910083313

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.