Molecular histopathology of matrix proteins through autofluorescence super-resolution microscopy

• Published in: Scientific reports Vol. 14; no. 1; p. 10524
• Main Authors: Ghosh, Biswajoy, Chatterjee, Jyotirmoy, Paul, Ranjan Rashmi, Acuña, Sebastian, Lahiri, Pooja, Pal, Mousumi, Mitra, Pabitra, Agarwal, Krishna
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 08.05.2024; Nature Publishing Group; Springer Nature; Nature Portfolio
• Subjects: 631/1647; 631/1647/245; 631/1647/328; 692/308; 692/4028; Animals; Collagen; Collagen - metabolism; Diagnosis; Extracellular matrix; Extracellular Matrix - metabolism; Extracellular Matrix Proteins - metabolism; Fibrils; Fibrosis; Histopathology; Humanities and Social Sciences; Humans; Mice; Microscopes; Microscopy; Microscopy, Fluorescence - methods; Mouth Mucosa - metabolism; Mouth Mucosa - pathology; multidisciplinary; Optical Imaging - methods; Science; Science (multidisciplinary); Skin - metabolism; Skin - pathology
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-024-61178-0

Extracellular matrix diseases like fibrosis are elusive to diagnose early on, to avoid complete loss of organ function or even cancer progression, making early diagnosis crucial. Imaging the matrix densities of proteins like collagen in fixed tissue sections with suitable stains and labels is a standard for diagnosis and staging. However, fine changes in matrix density are difficult to realize by conventional histological staining and microscopy as the matrix fibrils are finer than the resolving capacity of these microscopes. The dyes further blur the outline of the matrix and add a background that bottlenecks high-precision early diagnosis of matrix diseases. Here we demonstrate the multiple signal classification method-MUSICAL-otherwise a computational super-resolution microscopy technique to precisely estimate matrix density in fixed tissue sections using fibril autofluorescence with image stacks acquired on a conventional epifluorescence microscope. We validated the diagnostic and staging performance of the method in extracted collagen fibrils, mouse skin during repair, and pre-cancers in human oral mucosa. The method enables early high-precision label-free diagnosis of matrix-associated fibrotic diseases without needing additional infrastructure or rigorous clinical training.