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The Secret Life of Collagen: Temporal Changes in Nanoscale Fibrillar Pre-Strain and Molecular Organization during Physiological Loading of Cartilage.
Inamdar, Sheetal R; Knight, David P; Terrill, Nicholas J; Karunaratne, Angelo; Cacho-Nerin, Fernando; Knight, Martin M; Gupta, Himadri S.
Afiliación
  • Inamdar SR; Institute of Bioengineering, School of Engineering and Materials Science, Queen Mary University of London , London E1 4NS, United Kingdom.
  • Knight DP; Orthox Ltd. , 66 Innovation Drive, Milton Park, Abingdon OX14 4RQ, United Kingdom.
  • Terrill NJ; Harwell Science and Innovation Campus, Diamond Light Source , Harwell, Didcot OX11 0DE, United Kingdom.
  • Karunaratne A; Department of Bioengineering, Imperial College London , London SW7 2AZ, United Kingdom.
  • Cacho-Nerin F; Harwell Science and Innovation Campus, Diamond Light Source , Harwell, Didcot OX11 0DE, United Kingdom.
  • Knight MM; Institute of Bioengineering, School of Engineering and Materials Science, Queen Mary University of London , London E1 4NS, United Kingdom.
  • Gupta HS; Institute of Bioengineering, School of Engineering and Materials Science, Queen Mary University of London , London E1 4NS, United Kingdom.
ACS Nano ; 11(10): 9728-9737, 2017 10 24.
Article en En | MEDLINE | ID: mdl-28800220
Articular cartilage is a natural biomaterial whose structure at the micro- and nanoscale is critical for healthy joint function and where degeneration is associated with widespread disorders such as osteoarthritis. At the nanoscale, cartilage mechanical functionality is dependent on the collagen fibrils and hydrated proteoglycans that form the extracellular matrix. The dynamic response of these ultrastructural building blocks at the nanoscale, however, remains unclear. Here we measure time-resolved changes in collagen fibril strain, using small-angle X-ray diffraction during compression of bovine and human cartilage explants. We demonstrate the existence of a collagen fibril tensile pre-strain, estimated from the D-period at approximately 1-2%, due to osmotic swelling pressure from the proteoglycan. We reveal a rapid reduction and recovery of this pre-strain which occurs during stress relaxation, approximately 60 s after the onset of peak load. Furthermore, we show that this reduction in pre-strain is linked to disordering in the intrafibrillar molecular packing, alongside changes in the axial overlapping of tropocollagen molecules within the fibril. Tissue degradation in the form of selective proteoglycan removal disrupts both the collagen fibril pre-strain and the transient response during stress relaxation. This study bridges a fundamental gap in the knowledge describing time-dependent changes in collagen pre-strain and molecular organization that occur during physiological loading of articular cartilage. The ultrastructural details of this transient response are likely to transform our understanding of the role of collagen fibril nanomechanics in the biomechanics of cartilage and other hydrated soft tissues.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteoglicanos / Colágenos Fibrilares Límite: Animals / Humans Idioma: En Revista: ACS Nano Año: 2017 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteoglicanos / Colágenos Fibrilares Límite: Animals / Humans Idioma: En Revista: ACS Nano Año: 2017 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos