Evidence map›Paper›PMID 29032370›Full record

ArticleBiology open2017

An immunofluorescence assay for extracellular matrix components highlights the role of epithelial cells in producing a stable, fibrillar extracellular matrix.

Omar S Qureshi, Hélène Bon, Breda Twomey, Gill Holdsworth, Kirsty Ford, Marianne Bergin, Linghong Huang, Mariusz Muzylak, Louise J Healy, Vanessa Hurdowar and 1 more

Open access · goldAbstract read
In one paragraph

Article in Biology open, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

17 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
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  8. iMaterials today. Bio · 2024
    Article
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  11. Article
  12. Article
  13. In Vitro Liver Toxicity Testing of Chemicals: A Pragmatic Approach.International journal of molecular sciences · 2021
    Review
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  15. Article
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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

11 authors at 1 institution in 1 country.

Omar S QureshiUCB Pharma, Berkshire SL1 3WE, UK Omar.Qureshi@ucb.com Tim.Johnson@ucb.com.ORCID http://orcid.org/0000-0002-4737-4347
Hélène BonUCB Pharma, Berkshire SL1 3WE, UK.
Breda TwomeyUCB Pharma, Berkshire SL1 3WE, UK.
Gill HoldsworthUCB Pharma, Berkshire SL1 3WE, UK.
Kirsty FordUCB Pharma, Berkshire SL1 3WE, UK.
Marianne BerginUCB Pharma, Berkshire SL1 3WE, UK.
Linghong HuangUCB Pharma, Berkshire SL1 3WE, UK.
Mariusz MuzylakUCB Pharma, Berkshire SL1 3WE, UK.
Louise J HealyUCB Pharma, Berkshire SL1 3WE, UK.
Vanessa HurdowarUCB Pharma, Berkshire SL1 3WE, UK.
Timothy S JohnsonUCB Pharma, Berkshire SL1 3WE, UK Omar.Qureshi@ucb.com Tim.Johnson@ucb.com.
UCB Pharma (United Kingdom) · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Activated fibroblasts are considered major drivers of fibrotic disease progression through the production of excessive extracellular matrix (ECM) in response to signals from damaged epithelial and inflammatory cells. Nevertheless, epithelial cells are capable of expressing components of the ECM, cross-linking enzymes that increase its stability and are sensitive to factors involved in the early stages of fibrosis. We therefore wanted to test the hypothesis that epithelial cells can deposit ECM in response to stimulation in a comparable manner to fibroblasts. We performed immunofluorescence analysis of components of stable, mature extracellular matrix produced by primary human renal proximal tubular epithelial cells and renal fibroblasts in response to cytokine stimulation. Whilst fibroblasts produced a higher basal level of extracellular matrix components, epithelial cells were able to deposit significant levels of fibronectin, collagen I, III and IV in response to cytokine stimulation. In response to hypoxia, epithelial cells showed an increase in collagen IV deposition but not in response to the acute stress stimuli aristolochic acid or hydrogen peroxide. When epithelial cells were in co-culture with fibroblasts we observed significant increases in the level of matrix deposition which could be reduced by transforming growth factor beta (TGF-β) blockade. Our results highlight the role of epithelial cells acting as efficient producers of stable extracellular matrix which could contribute to renal tubule thickening in fibrosis.

Indexed as

CollagenEpithelial cellExtracellular matrixFibroblastFibronectinFibrosisKidneyTransforming growth factor beta (TGF-β)Transglutaminase

Identifiers

PMID29032370
PMCPMC5665462
OpenAlexW2766559760

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.