Abstract

Characterization of the molecular attributes and spatial arrangements of cells and features within complex human tissues provides a critical basis for understanding processes involved in development and disease. Moreover, the ability to automate steps in the analysis and interpretation of histological images that currently require manual inspection by pathologists could revolutionize medical diagnostics. Toward this end, we developed a new imaging approach called multidimensional microscopic molecular profiling (MMMP) that can measure several independent molecular properties in situ at subcellular resolution for the same tissue specimen. MMMP involves repeated cycles of antibody or histochemical staining, imaging, and signal removal, which ultimately can generate information analogous to a multidimensional flow cytometry analysis on intact tissue sections. We performed a MMMP analysis on a tissue microarray containing a diverse set of 102 human tissues using a panel of 15 informative antibody and 5 histochemical stains plus DAPI. Large-scale unsupervised analysis of MMMP data, and visualization of the resulting classifications, identified molecular profiles that were associated with functional tissue features. We then directly annotated H&E images from this MMMP series such that canonical histological features of interest (e.g. blood vessels, epithelium, red blood cells) were individually labeled. By integrating image annotation data, we identified molecular signatures that were associated with specific histological annotations and we developed statistical models for automatically classifying these features. The classification accuracy for automated histology labeling was objectively evaluated using a cross-validation strategy, and significant accuracy (with a median per-pixel rate of 77% per feature from 15 annotated samples) for de novo feature prediction was obtained. These results suggest that high-dimensional profiling may advance the development of computer-based systems for automatically parsing relevant histological and cellular features from molecular imaging data of arbitrary human tissue samples, and can provide a framework and resource to spur the optimization of these technologies.

Highlights

  • Microscopic examination of cellular morphology and structure is a classical approach that has provided an invaluable foundation for analyzing the function, development, and organization of complex tissues

  • We adapted multi-dimensional microscopic molecular profiling (MMMP) to be compatible with formalin-fixed paraffin embedded (FFPE) samples contained on a tissue microarray (TMA), enabling us to simultaneously analyze on the order of hundreds of distinct tissue sections in parallel

  • We repeated the antibody staining procedure for angiotensin I converting enzyme (Ace) on an independent tissue section generated from the same TMA to ensure that the MMMP cycling procedure did not interfere with successful antibody staining (S2 Fig)

Read more

Summary

Introduction

Microscopic examination of cellular morphology and structure is a classical approach that has provided an invaluable foundation for analyzing the function, development, and organization of complex tissues. Large-scale molecular studies based on microarray analysis, high-throughput sequencing, and proteomic approaches have clearly demonstrated the advantages of quantitative multi-dimensional profiling for identifying functionally important subtypes of cancers and other cellular states with important clinical ramifications [4,5,6]. These techniques often require physical disruption of the interrogated samples, which sacrifices critical spatial information related to the individual cells and their native positional arrangements and relationships within intact specimens. Technologies that enable the acquisition of high-dimensional molecular profiles while retaining the spatial integrity of the examined material offer great potential for advancing the detailed characterization of important biological samples

Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.