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Structured illumination microscopy and automatized image processing as a rapid diagnostic tool for podocyte effacement

The morphology of podocyte foot processes is obligatory for renal function. Here we describe a method for the superresolution-visualization of podocyte foot processes using structured illumination microscopy of the slit diaphragm, which before has only been achieved by electron microscopy. As a proo...

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Autores principales: Siegerist, Florian, Ribback, Silvia, Dombrowski, Frank, Amann, Kerstin, Zimmermann, Uwe, Endlich, Karlhans, Endlich, Nicole
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5597580/
https://www.ncbi.nlm.nih.gov/pubmed/28904359
http://dx.doi.org/10.1038/s41598-017-11553-x
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author Siegerist, Florian
Ribback, Silvia
Dombrowski, Frank
Amann, Kerstin
Zimmermann, Uwe
Endlich, Karlhans
Endlich, Nicole
author_facet Siegerist, Florian
Ribback, Silvia
Dombrowski, Frank
Amann, Kerstin
Zimmermann, Uwe
Endlich, Karlhans
Endlich, Nicole
author_sort Siegerist, Florian
collection PubMed
description The morphology of podocyte foot processes is obligatory for renal function. Here we describe a method for the superresolution-visualization of podocyte foot processes using structured illumination microscopy of the slit diaphragm, which before has only been achieved by electron microscopy. As a proof of principle, we measured a mean foot process width of 0.249 ± 0.068 µm in healthy kidneys and a significant higher mean foot process width of 0.675 ± 0.256 µm in minimal change disease patients indicating effacement of foot processes. We then hypothesized that the slit length per glomerular capillary surface area (slit diaphragm density) could be used as an equivalent for the diagnosis of effacement. Using custom-made software we measured a mean value of 3.10 ± 0.27 µm(−1) in healthy subjects and 1.83 ± 0.49 µm(−1) in the minimal change disease patients. As foot process width was highly correlated with slit diaphragm density (R(2) = 0.91), we concluded that our approach is a valid method for the diagnosis of foot process effacement. In summary, we present a new technique to quantify podocyte damage, which combines superresolution microscopy with automatized image processing. Due to its diverse advantages, we propose this technique to be included into routine diagnostics of glomerular histopathology.
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spelling pubmed-55975802017-09-15 Structured illumination microscopy and automatized image processing as a rapid diagnostic tool for podocyte effacement Siegerist, Florian Ribback, Silvia Dombrowski, Frank Amann, Kerstin Zimmermann, Uwe Endlich, Karlhans Endlich, Nicole Sci Rep Article The morphology of podocyte foot processes is obligatory for renal function. Here we describe a method for the superresolution-visualization of podocyte foot processes using structured illumination microscopy of the slit diaphragm, which before has only been achieved by electron microscopy. As a proof of principle, we measured a mean foot process width of 0.249 ± 0.068 µm in healthy kidneys and a significant higher mean foot process width of 0.675 ± 0.256 µm in minimal change disease patients indicating effacement of foot processes. We then hypothesized that the slit length per glomerular capillary surface area (slit diaphragm density) could be used as an equivalent for the diagnosis of effacement. Using custom-made software we measured a mean value of 3.10 ± 0.27 µm(−1) in healthy subjects and 1.83 ± 0.49 µm(−1) in the minimal change disease patients. As foot process width was highly correlated with slit diaphragm density (R(2) = 0.91), we concluded that our approach is a valid method for the diagnosis of foot process effacement. In summary, we present a new technique to quantify podocyte damage, which combines superresolution microscopy with automatized image processing. Due to its diverse advantages, we propose this technique to be included into routine diagnostics of glomerular histopathology. Nature Publishing Group UK 2017-09-13 /pmc/articles/PMC5597580/ /pubmed/28904359 http://dx.doi.org/10.1038/s41598-017-11553-x Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Siegerist, Florian
Ribback, Silvia
Dombrowski, Frank
Amann, Kerstin
Zimmermann, Uwe
Endlich, Karlhans
Endlich, Nicole
Structured illumination microscopy and automatized image processing as a rapid diagnostic tool for podocyte effacement
title Structured illumination microscopy and automatized image processing as a rapid diagnostic tool for podocyte effacement
title_full Structured illumination microscopy and automatized image processing as a rapid diagnostic tool for podocyte effacement
title_fullStr Structured illumination microscopy and automatized image processing as a rapid diagnostic tool for podocyte effacement
title_full_unstemmed Structured illumination microscopy and automatized image processing as a rapid diagnostic tool for podocyte effacement
title_short Structured illumination microscopy and automatized image processing as a rapid diagnostic tool for podocyte effacement
title_sort structured illumination microscopy and automatized image processing as a rapid diagnostic tool for podocyte effacement
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5597580/
https://www.ncbi.nlm.nih.gov/pubmed/28904359
http://dx.doi.org/10.1038/s41598-017-11553-x
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