Multiscale X-ray phase contrast imaging of human cartilage for investigating osteoarthritis formation.


Journal

Journal of biomedical science
ISSN: 1423-0127
Titre abrégé: J Biomed Sci
Pays: England
ID NLM: 9421567

Informations de publication

Date de publication:
07 Jun 2021
Historique:
received: 09 01 2021
accepted: 01 06 2021
entrez: 8 6 2021
pubmed: 9 6 2021
medline: 30 9 2021
Statut: epublish

Résumé

The evolution of cartilage degeneration is still not fully understood, partly due to its thinness, low radio-opacity and therefore lack of adequately resolving imaging techniques. X-ray phase-contrast imaging (X-PCI) offers increased sensitivity with respect to standard radiography and CT allowing an enhanced visibility of adjoining, low density structures with an almost histological image resolution. This study examined the feasibility of X-PCI for high-resolution (sub-) micrometer analysis of different stages in tissue degeneration of human cartilage samples and compare it to histology and transmission electron microscopy. Ten 10%-formalin preserved healthy and moderately degenerated osteochondral samples, post-mortem extracted from human knee joints, were examined using four different X-PCI tomographic set-ups using synchrotron radiation the European Synchrotron Radiation Facility (France) and the Swiss Light Source (Switzerland). Volumetric datasets were acquired with voxel sizes between 0.7 × 0.7 × 0.7 and 0.1 × 0.1 × 0.1 µm X-PCI provides a three-dimensional visualization of healthy and moderately degenerated cartilage samples down to a (sub-)cellular level with good correlation to histologic and transmission electron microscopy images. X-PCI is able to resolve the three layers and the architectural organization of cartilage including changes in chondrocyte cell morphology, chondrocyte subgroup distribution and (re-)organization as well as its subtle matrix structures. X-PCI captures comprehensive cartilage tissue transformation in its environment and might serve as a tissue-preserving, staining-free and volumetric virtual histology tool for examining and chronicling cartilage behavior in basic research/laboratory experiments of cartilage disease evolution.

Sections du résumé

BACKGROUND BACKGROUND
The evolution of cartilage degeneration is still not fully understood, partly due to its thinness, low radio-opacity and therefore lack of adequately resolving imaging techniques. X-ray phase-contrast imaging (X-PCI) offers increased sensitivity with respect to standard radiography and CT allowing an enhanced visibility of adjoining, low density structures with an almost histological image resolution. This study examined the feasibility of X-PCI for high-resolution (sub-) micrometer analysis of different stages in tissue degeneration of human cartilage samples and compare it to histology and transmission electron microscopy.
METHODS METHODS
Ten 10%-formalin preserved healthy and moderately degenerated osteochondral samples, post-mortem extracted from human knee joints, were examined using four different X-PCI tomographic set-ups using synchrotron radiation the European Synchrotron Radiation Facility (France) and the Swiss Light Source (Switzerland). Volumetric datasets were acquired with voxel sizes between 0.7 × 0.7 × 0.7 and 0.1 × 0.1 × 0.1 µm
RESULTS RESULTS
X-PCI provides a three-dimensional visualization of healthy and moderately degenerated cartilage samples down to a (sub-)cellular level with good correlation to histologic and transmission electron microscopy images. X-PCI is able to resolve the three layers and the architectural organization of cartilage including changes in chondrocyte cell morphology, chondrocyte subgroup distribution and (re-)organization as well as its subtle matrix structures.
CONCLUSIONS CONCLUSIONS
X-PCI captures comprehensive cartilage tissue transformation in its environment and might serve as a tissue-preserving, staining-free and volumetric virtual histology tool for examining and chronicling cartilage behavior in basic research/laboratory experiments of cartilage disease evolution.

Identifiants

pubmed: 34098949
doi: 10.1186/s12929-021-00739-1
pii: 10.1186/s12929-021-00739-1
pmc: PMC8182937
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

42

Subventions

Organisme : Deutsche Forschungsgemeinschaft (Cluster of Excellence) Munich Center for Advanced Photonics
ID : EXE158

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Auteurs

Annie Horng (A)

Department of Clinical Radiology, Faculty of Medicine, Ludwig-Maximilians-University, Marchioninistr. 15, 81377, Munich, Germany.
RZM - Radiologisches Zentrum Munich-Pasing, Pippinger Str. 25, 81245, Munich, Germany.

Johannes Stroebel (J)

Department of Medical Physics, Faculty of Physics, Ludwig-Maximilians-University Munich, Am Coulombwall 1, 85748, Garching, Germany.

Tobias Geith (T)

Department of Interventional Radiology, Klinikum Rechts der Isar of the Technical University of Munich, Munich, Germany.

Stefan Milz (S)

Faculty of Medicine, Anatomische Anstalt, Neuroanatomy, Ludwig Maximilians University, Munich, Germany.

Alexandra Pacureanu (A)

European Synchrotron Radiation Facility, Grenoble, France.

Yang Yang (Y)

European Synchrotron Radiation Facility, Grenoble, France.
National Synchrotron Light Source II, Brookhaven National Laboratory, Upton, NY, 11973, USA.

Peter Cloetens (P)

European Synchrotron Radiation Facility, Grenoble, France.

Goran Lovric (G)

Paul Scherrer Institute (Swiss Light Source), Villigen, Switzerland.

Alberto Mittone (A)

CELLS: ALBA Synchrotron, Barcelona, Spain.

Alberto Bravin (A)

European Synchrotron Radiation Facility, Grenoble, France.

Paola Coan (P)

Department of Clinical Radiology, Faculty of Medicine, Ludwig-Maximilians-University, Marchioninistr. 15, 81377, Munich, Germany. Paola.Coan@physik.uni-muenchen.de.
Department of Medical Physics, Faculty of Physics, Ludwig-Maximilians-University Munich, Am Coulombwall 1, 85748, Garching, Germany. Paola.Coan@physik.uni-muenchen.de.

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