Abstract

BackgroundThree-dimensional imaging modalities for optically dense connective tissues such as tendons are limited and typically have a single imaging methodological endpoint. Here, we have developed a bimodal procedure utilising fluorescence-based confocal microscopy and x-ray micro-computed tomography for the imaging of adult tendons to visualise and analyse extracellular sub-structure and cellular composition in small and large animal species.ResultsUsing fluorescent immunolabelling and optical clearing, we visualised the expression of the novel cross-species marker of tendon basement membrane, laminin-α4 in 3D throughout whole rat Achilles tendons and equine superficial digital flexor tendon 5 mm segments. This revealed a complex network of laminin-α4 within the tendon core that predominantly localises to the interfascicular matrix compartment. Furthermore, we implemented a chemical drying process capable of creating contrast densities enabling visualisation and quantification of both fascicular and interfascicular matrix volume and thickness by x-ray micro-computed tomography. We also demonstrated that both modalities can be combined using reverse clarification of fluorescently labelled tissues prior to chemical drying to enable bimodal imaging of a single sample.ConclusionsWhole-mount imaging of tendon allowed us to identify the presence of an extensive network of laminin-α4 within tendon, the complexity of which cannot be appreciated using traditional 2D imaging techniques. Creating contrast for x-ray micro-computed tomography imaging of tendon using chemical drying is not only simple and rapid, but also markedly improves on previously published methods. Combining these methods provides the ability to gain spatio-temporal information and quantify tendon substructures to elucidate the relationship between morphology and function.

Highlights

  • Advances in 3-dimensional (3D) imaging of dense connective tissues such as tendons are essential for the investigation of normal tissue structure as well as musculoskeletal diseases in pre-clinical models and clinical samples

  • To develop a method that enables both fluorescent imaging of cell-extracellular matrix (ECM) architecture and x-ray scanning of dense connective tissue structure, we combined multiple processes to create a workflow that integrates wholemount immunolabelling, reversible optical clarification, and subsequent chemical drying to enable bimodal 3D imaging of tendon by confocal microscopy and x-ray micro-computed tomography (μ-CT) (Fig. 1). We applied this technique to whole rat Achilles tendons and segments of equine superficial digital flexor tendons (SDFT)

  • Thereafter, we performed tissue immunolabelling and optical clarification with Visikol HISTOTM solutions to visualise 3D organisation of Laminin Alpha-4 (LAMA4) in whole rat Achilles and in segments of equine SDFT using confocal microscopy and optimised protocols based on size-specific guidelines provided by VisikolTM

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Summary

Introduction

Advances in 3-dimensional (3D) imaging of dense connective tissues such as tendons are essential for the investigation of normal tissue structure as well as musculoskeletal diseases in pre-clinical models and clinical samples. Until recently, imaging techniques to investigate both structural and cellular elements of dense collagenous tissues such as adult tendon have been limited to conventional 2D methods. These only allow appreciation of tissue structure in a single plane or require extensive reconstruction [5], and are time-consuming, labourintensive, and destructive, often creating artefacts within tissue [6]. We have developed a bimodal procedure utilising fluorescence-based confocal microscopy and x-ray micro-computed tomography for the imaging of adult tendons to visualise and analyse extracellular sub-structure and cellular composition in small and large animal species

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