Biology subjects

Disney, C. M.

Publications and source records attributed to Disney, C. M..

3 recordsLinked to original sources

bioRxiv2026

Regulation and function of trans-physeal growth plate bridges: evidence for a mechanical base isolation role to minimise epiphyseal shear stress

The cartilaginous growth plate (GP) is responsible for all bone elongation during post-natal growth yet must simultaneously contribute to mechanical epiphyseal stability for articulation. How the GP balances these dual functions across the bone-cartilage-bone epiphyseal interface during complex load-growth transitions is not defined. Herein, we examine regulation and mechanobiology of GP bridges - mineralised trans-physeal GP structures - to explore whether they serve these dual GP functions. We have determined the effects of age and sex, short- and long-term joint loading and several established and new osteotropic pharmacological agents on mouse tibial GP bridge number and areal density using micro-computed tomography. We also explored temporal formation and progression of GP bridges by serial in vivo scanning and we imaged epiphyseal load-transfer in young and mature mice in situ via synchrotron X-ray computed tomography (sCT) of intact joints under physiologically oriented load. Our utilisation of digital volume correlation revealed regional 3D load-induced strain inhomogeneities in the GP that are synchronised to bridge location and this was substantiated using finite element modelling. Furthermore, direct micro- and sCT examinations showed that bridges consistently contain a singular epiphyseal/metaphyseal discontinuity which appear to serve a novel mechanical base isolation role to minimise shear stress across the GP. Our data indicate that bridges are regulatable, dynamic structures that synchronise GP strains and exhibit sensitivity to local joint mechanics. We highlight that trans-physeal bridges may contribute to longitudinal bone growth cessation whilst simultaneously stabilising the epiphysis by absorbing compression and shear strains.

bioengineering↗

bioRxiv2025

Preserving Tissue Integrity Under the Beam: High-Energy, Low-Dose Synchrotron CT for in situ Imaging of Bovine Intervertebral Discs

In situ tomography enables non-destructive, time-lapse imaging of biological tissues under load, offering insights into structural and mechanical changes. However, repeated scans can expose samples to high radiation doses, potentially altering tissue properties. This study evaluated the feasibility of low-dose synchrotron computed tomography (sCT) for high-resolution, in situ imaging of intact bovine intervertebral discs (IVDs), and assessed the effects of repeated X-ray exposure on mechanical, microstructural, and molecular integrity. Intact oxtail IVD segments were imaged using propagation-based phase contrast sCT at 54 keV. Scan parameters were optimised to achieve high image quality within 66 seconds per scan, resulting in a total dose of ~30 kGy over six scans. Mechanical properties were assessed under cyclic loading, microstructural changes via digital volume correlation (DVC), and molecular alterations using Raman spectroscopy. High-resolution imaging of soft and calcified tissues was achieved. Changes in sample stiffness, hysteresis, or stress recovery between irradiated and control were not identified. DVC revealed no microstructural damage or strain accumulation in the calcified endplate. Raman spectroscopy indicated minimal changes in soft tissues, with bone showing slight increased collagen crosslinking and reduced mineralisation. Overall, this study demonstrates that high-energy, low-dose sCT enables repeated imaging of musculoskeletal tissues without compromising integrity, supporting its application in dynamic, time-lapse imaging studies. Importantly, larger, intact samples--such as whole bovine IVDs-- were imaged overcoming limitations of previous studies that relied on small animal models. This approach supports more physiologically relevant investigations of tissue mechanics and degeneration in complex systems.

bioengineering↗

bioRxiv2024

Multimodal imaging reveals multiscale mechanical interplay in vertebral endplate microarchitecture during intervertebral disc loading

The function of all musculoskeletal joints depends on hierarchical structures spanning the molecular to whole joint scales. Investigating biomechanics across length scales requires correlative multiscale experimental methods. This study applies multimodal in situ synchrotron imaging techniques to spinal joints - focussing on the vertebral endplates - to explore relationships between structure and mechanical strain across spatial scales. Strain mapping using digital volume correlation combined with microarchitectural analysis reveals that high tensile and shear strains play a role in the cartilage to bone transition. Correlative imaging and diffraction show that bone contains narrower mineral nano-crystallites under greater compressive prestrain compared to calcified cartilage. We hypothesise that this multiscale structural adaptation supports the mechanical function of the intervertebral disc. Future applications of the techniques presented here have potential to help unravel biomechanical underpinnings of pathologies affecting mineralised tissue structure. The multiscale structure-function relationships uncovered here may inspire the design of biomaterials and orthopaedic implants.

bioengineering↗