Propagation phase-contrast micro-computed tomography allows laboratory-based three-dimensional imaging of articular cartilage down to the cellular level.


Journal

Osteoarthritis and cartilage
ISSN: 1522-9653
Titre abrégé: Osteoarthritis Cartilage
Pays: England
ID NLM: 9305697

Informations de publication

Date de publication:
01 2020
Historique:
received: 02 05 2019
revised: 31 08 2019
accepted: 03 10 2019
pubmed: 5 11 2019
medline: 7 2 2021
entrez: 4 11 2019
Statut: ppublish

Résumé

High-resolution non-invasive three-dimensional (3D) imaging of chondrocytes in articular cartilage remains elusive. The aim of this study was to explore whether laboratory micro-computed tomography (micro-CT) permits imaging cells within articular cartilage. Bovine osteochondral plugs were prepared four ways: in phosphate-buffered saline (PBS) or 70% ethanol (EtOH), both with or without phosphotungstic acid (PTA) staining. Specimens were imaged with micro-CT following two protocols: 1) absorption contrast (AC) imaging 2) propagation phase-contrast (PPC) imaging. All samples were scanned in liquid. The contrast to noise ratio (C/N) of cellular features quantified scan quality and were statistically analysed. Cellular features resolved by micro-CT were validated by standard histology. The highest quality images were obtained using propagation phase-contrast imaging and PTA-staining in 70% EtOH. Cellular features were also visualised when stained in PBS and unstained in EtOH. Under all conditions PPC resulted in greater contrast than AC (p < 0.0001 to p = 0.038). Simultaneous imaging of cartilage and subchondral bone did not impede image quality. Corresponding features were located in both histology and micro-CT and followed the same distribution with similar density and roundness values. Three-dimensional visualisation and quantification of the chondrocyte population within articular cartilage can be achieved across a field of view of several millimetres using laboratory-based micro-CT. The ability to map chondrocytes in 3D opens possibilities for research in fields from skeletal development through to medical device design and treatment of cartilage degeneration.

Identifiants

pubmed: 31678663
pii: S1063-4584(19)31242-7
doi: 10.1016/j.joca.2019.10.007
pii:
doi:

Substances chimiques

Contrast Media 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

102-111

Subventions

Organisme : Medical Research Council
ID : MR/R025673/1
Pays : United Kingdom

Informations de copyright

Copyright © 2019 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.

Auteurs

J N Clark (JN)

Department of Mechanical Engineering, Imperial College London, London, UK. Electronic address: j.clark14@imperial.ac.uk.

A Garbout (A)

Imaging and Analysis Centre, Natural History Museum London, London, UK. Electronic address: amin.garbout@gmail.com.

S A Ferreira (SA)

National Heart & Lung Institute, Faculty of Medicine, Imperial College London, London, UK. Electronic address: s.ferreira@imperial.ac.uk.

B Javaheri (B)

Skeletal Biology Group, Comparative Biomedical Sciences, Royal Veterinary College, UK. Electronic address: bjavaheri@rvc.ac.uk.

A A Pitsillides (AA)

Skeletal Biology Group, Comparative Biomedical Sciences, Royal Veterinary College, UK. Electronic address: apitsillides@rvc.ac.uk.

S M Rankin (SM)

National Heart & Lung Institute, Faculty of Medicine, Imperial College London, London, UK. Electronic address: s.rankin@imperial.ac.uk.

J R T Jeffers (JRT)

Department of Mechanical Engineering, Imperial College London, London, UK. Electronic address: j.jeffers@imperial.ac.uk.

U Hansen (U)

Department of Mechanical Engineering, Imperial College London, London, UK. Electronic address: u.hansen@imperial.ac.uk.

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Classifications MeSH