An end-to-end workflow for non-destructive 3D pathology

Author:

Bishop Kevin W.ORCID,Barner Lindsey A. ErionORCID,Han Qinghua,Baraznenok Elena,Lan Lydia,Poudel ChetanORCID,Gao Gan,Serafin Robert B.ORCID,Chow Sarah S.L.,Glaser Adam K.ORCID,Janowczyk Andrew,Brenes DavidORCID,Huang Hongyi,Miyasato DominieORCID,True Lawrence D.,Kang Soyoung,Vaughan Joshua C.ORCID,Liu Jonathan T.C.ORCID

Abstract

AbstractRecent advances in 3D pathology offer the ability to image orders-of-magnitude more tissue than conventional pathology while providing a volumetric context that is lacking with 2D tissue sections, all without requiring destructive tissue sectioning. Generating high-quality 3D pathology datasets on a consistent basis is non-trivial, requiring careful attention to many details regarding tissue preparation, imaging, and data/image processing in an iterative process. Here we provide an end-to-end protocol covering all aspects of a 3D pathology workflow (using light-sheet microscopy as an illustrative imaging platform) with sufficient detail to perform well-controlled preclinical and clinical studies. While 3D pathology is compatible with diverse staining protocols and computationally generated color palettes for visual analysis, this protocol will focus on a fluorescent analog of hematoxylin and eosin (H&E), which remains the most common stain for gold-standard diagnostic determinations. We present our guidelines for a broad range of end-users (e.g., biologists, clinical researchers, and engineers) in a simple tutorial format.

Publisher

Cold Spring Harbor Laboratory

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