Evidence map›Paper›PMID 36675222›Full record

ArticleInternational journal of molecular sciences2023

Multi-Step Extracellular Matrix Remodelling and Stiffening in the Development of Idiopathic Pulmonary Fibrosis.

Constança Júnior, Anna Ulldemolins, Maria Narciso, Isaac Almendros, Ramon Farré, Daniel Navajas, Javier López, Mar Eroles, Felix Rico, Núria Gavara

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
8.3field-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

22 citing papers in PubMed, 32 citations in OpenAlex.

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  8. Mechanobiology and Resolution of Lung Fibrosis.Annual review of physiology · 2026
    Review
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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

10 authors at 3 institutions in 2 countries.

Constança JúniorUnitat de Biofísica i Bioenginyeria, Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona, 08036 Barcelona, Spain.ORCID 0000-0002-3985-9213
Anna UlldemolinsUnitat de Biofísica i Bioenginyeria, Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona, 08036 Barcelona, Spain.ORCID 0000-0001-8825-9436
Maria NarcisoUnitat de Biofísica i Bioenginyeria, Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona, 08036 Barcelona, Spain.ORCID 0000-0002-4994-1691
Isaac AlmendrosUnitat de Biofísica i Bioenginyeria, Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona, 08036 Barcelona, Spain.ORCID 0000-0002-1998-9379
Ramon FarréUnitat de Biofísica i Bioenginyeria, Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona, 08036 Barcelona, Spain.ORCID 0000-0002-9084-7824
Daniel NavajasUnitat de Biofísica i Bioenginyeria, Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona, 08036 Barcelona, Spain.
Javier LópezInstitut Pasteur de Lille, U1019-UMR9017-CIIL-Centre d'Infection et d'Immunité de Lille, Université de Lille, CNRS, Inserm, CHU Lille, 59000 Lille, France.
Mar ErolesAix-Marseille, CNRS, INSERM, LAI, Centuri Centre for Living Systems, 13009 Marseille, France.ORCID 0000-0003-3571-0769
Felix RicoAix-Marseille, CNRS, INSERM, LAI, Centuri Centre for Living Systems, 13009 Marseille, France.ORCID 0000-0002-7757-8340
Núria GavaraUnitat de Biofísica i Bioenginyeria, Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona, 08036 Barcelona, Spain.ORCID 0000-0002-7666-110X
Centro de Investigación Biomédica en Red de Enfermedades Respiratorias · ESCentre National de la Recherche Scientifique · FRInstitute for Bioengineering of Catalonia · ES

Funding

H2020 European Research and Innovation Programme 812772Ministerio de Ciencia e Innovación PID2020-116808RB-I00 AEI-RetosMinisterio de Ciencia e Innovación PID2020- 520 113910RB-I00-AEI/10.13039/501100011033Ministerio de Ciencia e Innovación SAF2017-85574-RSociedad Española de Neumología y Cirugía Torácica 900-2019
6 · The paper itself

Abstract

The extracellular matrix (ECM) of the lung is a filamentous network composed mainly of collagens, elastin, and proteoglycans that provides structural and physical support to its populating cells. Proliferation, migration and overall behaviour of those cells is greatly determined by micromechanical queues provided by the ECM. Lung fibrosis displays an aberrant increased deposition of ECM which likely changes filament organization and stiffens the ECM, thus upregulating the profibrotic profile of pulmonary cells. We have previously used AFM to assess changes in the Young's Modulus (E) of the ECM in the lung. Here, we perform further ECM topographical, mechanical and viscoelastic analysis at the micro- and nano-scale throughout fibrosis development. Furthermore, we provide nanoscale correlations between topographical and elastic properties of the ECM fibres. Firstly, we identify a softening of the ECM after rats are instilled with media associated with recovery of mechanical homeostasis, which is hindered in bleomycin-instilled lungs. Moreover, we find opposite correlations between fibre stiffness and roughness in PBS- vs bleomycin-treated lung. Our findings suggest that changes in ECM nanoscale organization take place at different stages of fibrosis, with the potential to help identify pharmacological targets to hinder its progression.

Indexed as

Extracellular MatrixIdiopathic Pulmonary FibrosisAnimalsBleomycinFibrosisLungRatsBleomycinatomic force microscopyextracellular matrixidiopathic pulmonary fibrosismechanosensing

Identifiers

PMID36675222
PMCPMC9865994
OpenAlexW4316371646

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.