Abstract

Damage and degradation of articular cartilage leads to severe pain and loss of mobility. The development of new therapies for cartilage regeneration for monitoring their effect requires further study of cartilage, ideally at a molecular level and in a minimally invasive way. Hyperspectral microscopy is a novel technology which utilises endogenous fluorophores to non-invasively assess the molecular composition of cells and tissue. In this study, we applied hyperspectral microscopy to healthy bovine articular cartilage and osteoarthritic human articular cartilage to investigate its capacity to generate informative molecular data and characterise disease state and treatment effects. We successfully demonstrated label-free fluorescence identification of collagen type I and II – isolated in cartilage here for the first time and the co-enzymes free NADH and FAD which together give the optical redox ratio that is an important measure of metabolic activity. The intracellular composition of chondrocytes was also examined. Differences were observed in the molecular ratios within the superficial and transitional zones of the articular cartilage which appeared to be influenced by disease state and treatment. These findings show that hyperspectral microscopy could be useful for investigating the molecular underpinnings of articular cartilage degradation and repair. As it is non-invasive and non-destructive, samples can be repeatedly assessed over time, enabling true time-course experiments with in-depth molecular data. Additionally, there is potential for the hyperspectral approach to be adapted for patient examination to allow the investigation of cartilage state. This could be of advantage for assessment and diagnosis as well as treatment monitoring.

Highlights

  • Www.nature.com/scientificreports regeneration, as well as techniques for monitoring their effect will require further study of cartilage, ideally on a molecular level and in a minimally invasive way

  • We have applied this methodology to examine the native distribution of endogenous tissue fluorophores in intact articular cartilage, and subsequently demonstrated the potential of our methodology to characterise the effects of an experimental treatment of osteoarthritic (OA) cartilage performed ex vivo

  • In the superficial layer this component was less abundant than collagen types I and II, while in the transitional layer the relative amount of unknown matrix component (UMC) was comparable to that of collagen II

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Summary

Introduction

Www.nature.com/scientificreports regeneration, as well as techniques for monitoring their effect will require further study of cartilage, ideally on a molecular level and in a minimally invasive way. Immunohistochemistry can identify collagen type I and II in cartilage, and this approach has been used in the literature to explore cartilage regeneration study[16] These conventional methods are laborious, costly, invasive and can only provide a snapshot of a tissue structure and its functional state on a sample-by-sample basis. Our approach is based on multispectral imaging of tissue autofluorescence followed by unmixing of the fluorescence signals of individual compounds native to cartilage, identified using a previously reported unmixing approach[17] These compounds, most notably nicotinamide adenine dinucleotide (NADH) and flavin adenine dinucleotide (FAD), can provide informative signatures of cellular metabolic activity[18,19,20]. Especially collagen type II significantly contribute to the strong intrinsic fluorescence of cartilage[25,26]

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