Evidence map›Paper›PMID 31374336›Full record

ArticleActa biomaterialia2019

Proteoglycan degradation mimics static compression by altering the natural gradients in fibrillar organisation in cartilage.

Sheetal R Inamdar, Ettore Barbieri, Nicholas J Terrill, Martin M Knight, Himadri S Gupta

Open access · hybridAbstract read
In one paragraph

Article in Acta biomaterialia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 31 citations in OpenAlex.

  1. The Impact of Ageing on Fibrillar Collagens.Sub-cellular biochemistry · 2026
    Review
  2. Review
  3. Article
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  7. Article
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  10. Spatiotemporal Measurement of Osmotic Pressures by FRET Imaging.Angewandte Chemie (International ed. in English) · 2021
    Article
  11. AnFrontiers in bioengineering and biotechnology · 2021
    Article
  12. 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

5 authors at 3 institutions in 2 countries.

Sheetal R InamdarInstitute of Bioengineering and School of Engineering and Material Science, Queen Mary University of London, London E1 4NS, United Kingdom.
Ettore BarbieriCenter for Mathematical Science and Advanced Technology, Research Institute for Value-Added Information Generation, Japan Agency for Marine-Earth Science and Technology, 3173-25, Showa-machi, Kanazawa-ku, Yokohama-city, Japan.
Nicholas J TerrillHarwell Science and Innovation Campus, Diamond Light Source, Harwell, Didcot OX11 0DE, United Kingdom.
Martin M KnightInstitute of Bioengineering and School of Engineering and Material Science, Queen Mary University of London, London E1 4NS, United Kingdom.
Himadri S GuptaInstitute of Bioengineering and School of Engineering and Material Science, Queen Mary University of London, London E1 4NS, United Kingdom. Electronic address: h.gupta@qmul.ac.uk.
Queen Mary University of London · GBDiamond Light Source · GBJapan Agency for Marine-Earth Science and Technology · JP

Funding

Biotechnology and Biological Sciences Research Council BB/R003610/1Biotechnology and Biological Sciences Research Council BB/R004773/1Medical Research Council MR/R025673/1
6 · The paper itself

Abstract

Structural and associated biomechanical gradients within biological tissues are important for tissue functionality and preventing damaging interfacial stress concentrations. Articular cartilage possesses an inhomogeneous structure throughout its thickness, driving the associated variation in the biomechanical strain profile within the tissue under physiological compressive loading. However, little is known experimentally about the nanostructural mechanical role of the collagen fibrils and how this varies with depth. Utilising a high-brilliance synchrotron X-ray source, we have measured the depth-wise nanostructural parameters of the collagen network in terms of the periodic fibrillar banding (D-period) and associated parameters. We show that there is a depth dependent variation in D-period reflecting the pre-strain and concurrent with changes in the level of intrafibrillar order. Further, prolonged static compression leads to fibrillar changes mirroring those caused by removal of extrafibrillar proteoglycans (as may occur in aging or disease). We suggest that fibrillar D-period is a sensitive indicator of localised changes to the mechanical environment at the nanoscale in soft connective tissues. STATEMENT OF SIGNIFICANCE: Collagen plays a significant role in both the structural and mechanical integrity of articular cartilage, allowing the tissue to withstand highly repetitive loading. However, the fibrillar mechanics of the collagen network in cartilage are not clear. Here we find that cartilage has a spatial gradient in the nanostructural collagen fibril pre-strain, with an increase in the fibrillar pre-strain with depth. Further, the fibrillar gradient changes similarly under compression when compared to an enzymatically degraded tissue which mimics age-related changes. Given that the fibrils potentially have a finite capacity to mechanically respond and alter their configuration, these findings are significant in understanding how collagen may alter in structure and gradient in diseased cartilage, and in informing the design of cartilage replacements.

Indexed as

Compressive StrengthProteolysisStress, MechanicalAnimalsCartilageCattleProteoglycansProteoglycansBiomechanicsCartilageCollagen mechanicsNanostructureStructural gradients

Identifiers

PMID31374336
PMCPMC6838783
OpenAlexW2966584698

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.