Cargando…

Structured Illumination-Based Super-Resolution Optical Microscopy for Hemato- and Cyto-Pathology Applications

Structured illumination fluorescence microscopy utilizes interfering light and the moiré effect to enhance spatial resolution to about a half of that of conventional light microscopy, i.e. approximately 90 nm. In addition to the enhancement in the x and y directions, it also allows enhancement of re...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Tieqiao, Osborn, Samantha, Brandow, Chloe, Dwyre, Denis, Green, Ralph, Lane, Stephen, Wachsmann-Hogiu, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4605645/
https://www.ncbi.nlm.nih.gov/pubmed/23579249
http://dx.doi.org/10.3233/ACP-130075
_version_ 1782395234279227392
author Zhang, Tieqiao
Osborn, Samantha
Brandow, Chloe
Dwyre, Denis
Green, Ralph
Lane, Stephen
Wachsmann-Hogiu, Sebastian
author_facet Zhang, Tieqiao
Osborn, Samantha
Brandow, Chloe
Dwyre, Denis
Green, Ralph
Lane, Stephen
Wachsmann-Hogiu, Sebastian
author_sort Zhang, Tieqiao
collection PubMed
description Structured illumination fluorescence microscopy utilizes interfering light and the moiré effect to enhance spatial resolution to about a half of that of conventional light microscopy, i.e. approximately 90 nm. In addition to the enhancement in the x and y directions, it also allows enhancement of resolution in the z- direction by the same factor of two (to approximately 220 nm), making it a powerful tool for 3-D morphology studies of fluorescently labeled cells or thin tissue sections. In this report, we applied this technique to several types of blood cells that are commonly seen in hematopathology. Compared with standard brightfield and ordinary fluorescence microscopy images, the 3-D morphology results clearly reveal the morphological features of different types of normal blood cells. We have also used this technique to evaluate morphologies of abnormal erythrocytes and compare them with those recorded on normal cells. The results give a very intuitive presentation of morphological structures of erythrocytes with great details. This research illustrates the potential of this technique to be used in hematology and cyto-pathology studies aimed at identifying nanometer-sized features that cannot be distinguished otherwise with conventional optical microscopy.
format Online
Article
Text
id pubmed-4605645
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher IOS Press
record_format MEDLINE/PubMed
spelling pubmed-46056452015-12-13 Structured Illumination-Based Super-Resolution Optical Microscopy for Hemato- and Cyto-Pathology Applications Zhang, Tieqiao Osborn, Samantha Brandow, Chloe Dwyre, Denis Green, Ralph Lane, Stephen Wachsmann-Hogiu, Sebastian Anal Cell Pathol (Amst) Other Structured illumination fluorescence microscopy utilizes interfering light and the moiré effect to enhance spatial resolution to about a half of that of conventional light microscopy, i.e. approximately 90 nm. In addition to the enhancement in the x and y directions, it also allows enhancement of resolution in the z- direction by the same factor of two (to approximately 220 nm), making it a powerful tool for 3-D morphology studies of fluorescently labeled cells or thin tissue sections. In this report, we applied this technique to several types of blood cells that are commonly seen in hematopathology. Compared with standard brightfield and ordinary fluorescence microscopy images, the 3-D morphology results clearly reveal the morphological features of different types of normal blood cells. We have also used this technique to evaluate morphologies of abnormal erythrocytes and compare them with those recorded on normal cells. The results give a very intuitive presentation of morphological structures of erythrocytes with great details. This research illustrates the potential of this technique to be used in hematology and cyto-pathology studies aimed at identifying nanometer-sized features that cannot be distinguished otherwise with conventional optical microscopy. IOS Press 2013 2013-04-11 /pmc/articles/PMC4605645/ /pubmed/23579249 http://dx.doi.org/10.3233/ACP-130075 Text en Copyright © 2013 Hindawi Publishing Corporation and the authors.
spellingShingle Other
Zhang, Tieqiao
Osborn, Samantha
Brandow, Chloe
Dwyre, Denis
Green, Ralph
Lane, Stephen
Wachsmann-Hogiu, Sebastian
Structured Illumination-Based Super-Resolution Optical Microscopy for Hemato- and Cyto-Pathology Applications
title Structured Illumination-Based Super-Resolution Optical Microscopy for Hemato- and Cyto-Pathology Applications
title_full Structured Illumination-Based Super-Resolution Optical Microscopy for Hemato- and Cyto-Pathology Applications
title_fullStr Structured Illumination-Based Super-Resolution Optical Microscopy for Hemato- and Cyto-Pathology Applications
title_full_unstemmed Structured Illumination-Based Super-Resolution Optical Microscopy for Hemato- and Cyto-Pathology Applications
title_short Structured Illumination-Based Super-Resolution Optical Microscopy for Hemato- and Cyto-Pathology Applications
title_sort structured illumination-based super-resolution optical microscopy for hemato- and cyto-pathology applications
topic Other
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4605645/
https://www.ncbi.nlm.nih.gov/pubmed/23579249
http://dx.doi.org/10.3233/ACP-130075
work_keys_str_mv AT zhangtieqiao structuredilluminationbasedsuperresolutionopticalmicroscopyforhematoandcytopathologyapplications
AT osbornsamantha structuredilluminationbasedsuperresolutionopticalmicroscopyforhematoandcytopathologyapplications
AT brandowchloe structuredilluminationbasedsuperresolutionopticalmicroscopyforhematoandcytopathologyapplications
AT dwyredenis structuredilluminationbasedsuperresolutionopticalmicroscopyforhematoandcytopathologyapplications
AT greenralph structuredilluminationbasedsuperresolutionopticalmicroscopyforhematoandcytopathologyapplications
AT lanestephen structuredilluminationbasedsuperresolutionopticalmicroscopyforhematoandcytopathologyapplications
AT wachsmannhogiusebastian structuredilluminationbasedsuperresolutionopticalmicroscopyforhematoandcytopathologyapplications