Evidence map›Paper›PMID 35269067›Full record

ArticleMaterials (Basel, Switzerland)2022

Investigating the Fibrillar Ultrastructure and Mechanics in Keloid Scars Using In Situ Synchrotron X-ray Nanomechanical Imaging.

Yuezhou Zhang, Dave Hollis, Rosie Ross, Tim Snow, Nick J Terrill, Yongjie Lu, Wen Wang, John Connelly, Gianluca Tozzi, Himadri S Gupta

Open access · goldAbstract read
In one paragraph

Article in Materials (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
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 4 institutions in 1 country.

Yuezhou ZhangInstitute of Bioengineering and School of Engineering and Materials Science, Queen Mary University of London, London E1 4NS, UK.
Dave HollisLaVision UK, 2 Minton Place, Victoria Road, Bicester OX26 6QB, UK.
Rosie RossCentre for Cell Biology and Cutaneous Research, Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London E1 2AT, UK.
Tim SnowDiamond Light Source, Harwell Science and Innovation Campus, Didcot OX11 0DE, UK.ORCID 0000-0001-7146-6885
Nick J TerrillDiamond Light Source, Harwell Science and Innovation Campus, Didcot OX11 0DE, UK.ORCID 0000-0002-8783-1282
Yongjie LuCentre for Biomarkers and Biotherapeutics, Barts Cancer Institute, Queen Mary University of London, John Vane Science Centre, Charterhouse Square, London EC1M 5PZ, UK.
Wen WangInstitute of Bioengineering and School of Engineering and Materials Science, Queen Mary University of London, London E1 4NS, UK.
John ConnellyCentre for Cell Biology and Cutaneous Research, Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London E1 2AT, UK.
Gianluca TozziSchool of Engineering, London South Bank University, London SE1 0AA, UK.
Himadri S GuptaInstitute of Bioengineering and School of Engineering and Materials Science, Queen Mary University of London, London E1 4NS, UK.ORCID 0000-0003-2201-8933
Queen Mary University of London · GBDiamond Light Source · GBLaVision (United Kingdom) · GBLondon South Bank University · GB

Funding

Biotechnology and Biological Sciences Research Council BB/R003610/1, BB/R003610/1Engineering and Physical Sciences Research Council EP/V011235/1Medical Research Council MR/R025673/1Science and Technology Facilities Council SM-18524-2
6 · The paper itself

Abstract

Fibrotic scarring is prevalent in a range of collagenous tissue disorders. Understanding the role of matrix biophysics in contributing to fibrotic progression is important to develop therapies, as well as to elucidate biological mechanisms. Here, we demonstrate how microfocus small-angle X-ray scattering (SAXS), with in situ mechanics and correlative imaging, can provide quantitative and position-resolved information on the fibrotic matrix nanostructure and its mechanical properties. We use as an example the case of keloid scarring in skin. SAXS mapping reveals heterogeneous gradients in collagen fibrillar concentration, fibril pre-strain (variations in D-period) and a new interfibrillar component likely linked to proteoglycans, indicating evidence of a complex 3D structure at the nanoscale. Furthermore, we demonstrate a proof-of-principle for a diffraction-contrast correlative imaging technique, incorporating, for the first time, DIC and SAXS, and providing an initial estimate for measuring spatially resolved fibrillar-level strain and reorientation in such heterogeneous tissues. By application of the method, we quantify (at the microscale) fibrillar reorientations, increases in fibrillar D-period variance, and increases in mean D-period under macroscopic tissue strains of ~20%. Our results open the opportunity of using synchrotron X-ray nanomechanical imaging as a quantitative tool to probe structure-function relations in keloid and other fibrotic disorders in situ.

Indexed as

collagen fibrilsdigital image correlationextracellular matrixhypertrophic scarringkeloidsnanomechanicssmall-angle X-ray scatteringsynchrotron X-ray imaging

Identifiers

PMID35269067
PMCPMC8911729
OpenAlexW4214844908

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.