Open-Top Light-Sheet Microscopy Image Atlas of Prostate Core Needle Biopsies.

Arch Pathol Lab Med

From the Departments of Pathology (Drs Reder, True, and Liu and Ms McCarty) and Mechanical Engineering (Drs Glaser and Liu and Mr Chen), University of Washington, Seattle.

Published: September 2019

Context.—: Ex vivo microscopy encompasses a range of techniques to examine fresh or fixed tissue with microscopic resolution, eliminating the need to embed the tissue in paraffin or produce a glass slide. One such technique is light-sheet microscopy, which enables rapid 3D imaging. Our pathology-engineering collaboration has resulted in an open-top light-sheet (OTLS) microscope that is specifically tailored to the needs of pathology practice.

Objective.—: To present an image atlas of OTLS images of prostate core needle biopsies.

Design.—: Core needle biopsies (N = 9) were obtained from fresh radical prostatectomy specimens. Each biopsy was fixed in formalin, dehydrated in ethanol, stained with TO-PRO3 and eosin, optically cleared, and imaged using OTLS microscopy. The biopsies were then processed, paraffin embedded, and sectioned. Hematoxylin-eosin and immunohistochemical staining for cytokeratin 5 and cytokeratin 8 was performed.

Results.—: Benign and neoplastic histologic structures showed high fidelity between OTLS and traditional light microscopy. OTLS microscopy had no discernible effect on hematoxylin-eosin or immunohistochemical staining in this pilot study. The 3D histology information obtained using OTLS microscopy enabled new structural insights, including the observation of cribriform and well-formed gland morphologies within the same contiguous glandular structures, as well as the continuity of poorly formed glands with well-formed glands.

Conclusions.—: Three-dimensional OTLS microscopy images have a similar appearance to traditional hematoxylin-eosin histology images, with the added benefit of useful 3D structural information. Further studies are needed to continue to document the OTLS appearance of a wide range of tissues and to better understand 3D histologic structures.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7402418PMC
http://dx.doi.org/10.5858/arpa.2018-0466-OADOI Listing

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