Abstract

In the clinical practice of pathology, trichrome stains are commonly used to highlight collagen and to help evaluate fibrosis. Such stains do delineate collagen deposits but are not molecularly specific and can suffer from staining inconsistencies. Moreover, performing histochemical stain evaluation requires the preparation of additional sections beyond the original hematoxylin- and eosin-stained slides, as well as additional staining steps, which together add cost, time, and workflow complications. We have developed a new microscopy approach, termed DUET (DUal-mode Emission and Transmission) that can be used to extract signals that would typically require special stains or advanced optical methods. Our preliminary analysis demonstrates the potential of using the resulting signals to generate virtual histochemical images that resemble trichrome-stained slides and can support clinical evaluation. We demonstrate advantages of this approach over images acquired from conventional trichrome-stained slides and compare them with images created using second harmonic generation microscopy.

Highlights

  • Molecules from the collagen family comprise the main component of connective tissue and are the most abundant protein class in mammals [1]

  • A common sequela of ongoing tissue injury involves the development of fibrosis, namely an excess accumulation of extracellular matrix primarily composed of collagen

  • Similar structures are visible in both modes, there are some components that can be appreciated only in fluorescence, for example, the basement membrane structures identified by arrows in panels B and E

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Summary

Introduction

Molecules from the collagen family comprise the main component of connective tissue and are the most abundant protein class in mammals [1]. The overall extent of fibrosis reflects the level of irreversible end-organ injury and is the best recognized indicator for disease stage and prognosis This is especially true for medical diseases of the kidney and liver, as well as transplant pathology in these organs. It has been increasingly recognized that abnormal collagen composition and deposition is intimately involved in the interaction between cancers and their adjacent stroma, and subsequent tumor behavior can be shaped through mechanisms thought to involve tumor cell adhesion, proliferation, migration and invasion [2] These interactions can have profound impact on tumor progression and prognosis via imputed biochemical and mechanical mechanisms [3,4,5,6,7]

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