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Holographic virtual staining of individual biological cells

Many medical and biological protocols for analyzing individual biological cells involve morphological evaluation based on cell staining, designed to enhance imaging contrast and enable clinicians and biologists to differentiate between various cell organelles. However, cell staining is not always al...

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Autores principales: Nygate, Yoav N., Levi, Mattan, Mirsky, Simcha K., Turko, Nir A., Rubin, Moran, Barnea, Itay, Dardikman-Yoffe, Gili, Haifler, Miki, Shalev, Alon, Shaked, Natan T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196795/
https://www.ncbi.nlm.nih.gov/pubmed/32284403
http://dx.doi.org/10.1073/pnas.1919569117
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author Nygate, Yoav N.
Levi, Mattan
Mirsky, Simcha K.
Turko, Nir A.
Rubin, Moran
Barnea, Itay
Dardikman-Yoffe, Gili
Haifler, Miki
Shalev, Alon
Shaked, Natan T.
author_facet Nygate, Yoav N.
Levi, Mattan
Mirsky, Simcha K.
Turko, Nir A.
Rubin, Moran
Barnea, Itay
Dardikman-Yoffe, Gili
Haifler, Miki
Shalev, Alon
Shaked, Natan T.
author_sort Nygate, Yoav N.
collection PubMed
description Many medical and biological protocols for analyzing individual biological cells involve morphological evaluation based on cell staining, designed to enhance imaging contrast and enable clinicians and biologists to differentiate between various cell organelles. However, cell staining is not always allowed in certain medical procedures. In other cases, staining may be time-consuming or expensive to implement. Staining protocols may be operator-sensitive, and hence may lead to varying analytical results, as well as cause artificial imaging artifacts or false heterogeneity. We present a deep-learning approach, called HoloStain, which converts images of isolated biological cells acquired without staining by holographic microscopy to their virtually stained images. We demonstrate this approach for human sperm cells, as there is a well-established protocol and global standardization for characterizing the morphology of stained human sperm cells for fertility evaluation, but, on the other hand, staining might be cytotoxic and thus is not allowed during human in vitro fertilization (IVF). After a training process, the deep neural network can take images of unseen sperm cells retrieved from holograms acquired without staining and convert them to their stainlike images. We obtained a fivefold recall improvement in the analysis results, demonstrating the advantage of using virtual staining for sperm cell analysis. With the introduction of simple holographic imaging methods in clinical settings, the proposed method has a great potential to become a common practice in human IVF procedures, as well as to significantly simplify and radically change other cell analyses and techniques such as imaging flow cytometry.
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spelling pubmed-71967952020-05-06 Holographic virtual staining of individual biological cells Nygate, Yoav N. Levi, Mattan Mirsky, Simcha K. Turko, Nir A. Rubin, Moran Barnea, Itay Dardikman-Yoffe, Gili Haifler, Miki Shalev, Alon Shaked, Natan T. Proc Natl Acad Sci U S A Physical Sciences Many medical and biological protocols for analyzing individual biological cells involve morphological evaluation based on cell staining, designed to enhance imaging contrast and enable clinicians and biologists to differentiate between various cell organelles. However, cell staining is not always allowed in certain medical procedures. In other cases, staining may be time-consuming or expensive to implement. Staining protocols may be operator-sensitive, and hence may lead to varying analytical results, as well as cause artificial imaging artifacts or false heterogeneity. We present a deep-learning approach, called HoloStain, which converts images of isolated biological cells acquired without staining by holographic microscopy to their virtually stained images. We demonstrate this approach for human sperm cells, as there is a well-established protocol and global standardization for characterizing the morphology of stained human sperm cells for fertility evaluation, but, on the other hand, staining might be cytotoxic and thus is not allowed during human in vitro fertilization (IVF). After a training process, the deep neural network can take images of unseen sperm cells retrieved from holograms acquired without staining and convert them to their stainlike images. We obtained a fivefold recall improvement in the analysis results, demonstrating the advantage of using virtual staining for sperm cell analysis. With the introduction of simple holographic imaging methods in clinical settings, the proposed method has a great potential to become a common practice in human IVF procedures, as well as to significantly simplify and radically change other cell analyses and techniques such as imaging flow cytometry. National Academy of Sciences 2020-04-28 2020-04-13 /pmc/articles/PMC7196795/ /pubmed/32284403 http://dx.doi.org/10.1073/pnas.1919569117 Text en Copyright © 2020 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Physical Sciences
Nygate, Yoav N.
Levi, Mattan
Mirsky, Simcha K.
Turko, Nir A.
Rubin, Moran
Barnea, Itay
Dardikman-Yoffe, Gili
Haifler, Miki
Shalev, Alon
Shaked, Natan T.
Holographic virtual staining of individual biological cells
title Holographic virtual staining of individual biological cells
title_full Holographic virtual staining of individual biological cells
title_fullStr Holographic virtual staining of individual biological cells
title_full_unstemmed Holographic virtual staining of individual biological cells
title_short Holographic virtual staining of individual biological cells
title_sort holographic virtual staining of individual biological cells
topic Physical Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196795/
https://www.ncbi.nlm.nih.gov/pubmed/32284403
http://dx.doi.org/10.1073/pnas.1919569117
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