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Pancreas++: Automated Quantification of Pancreatic Islet Cells in Microscopy Images

The microscopic image analysis of pancreatic Islet of Langerhans morphology is crucial for the investigation of diabetes and metabolic diseases. Besides the general size of the islet, the percentage and relative position of glucagon-containing alpha-, and insulin-containing beta-cells is also import...

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Autores principales: Chen, Hongyu, Martin, Bronwen, Cai, Huan, Fiori, Jennifer L., Egan, Josephine M., Siddiqui, Sana, Maudsley, Stuart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3535421/
https://www.ncbi.nlm.nih.gov/pubmed/23293605
http://dx.doi.org/10.3389/fphys.2012.00482
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author Chen, Hongyu
Martin, Bronwen
Cai, Huan
Fiori, Jennifer L.
Egan, Josephine M.
Siddiqui, Sana
Maudsley, Stuart
author_facet Chen, Hongyu
Martin, Bronwen
Cai, Huan
Fiori, Jennifer L.
Egan, Josephine M.
Siddiqui, Sana
Maudsley, Stuart
author_sort Chen, Hongyu
collection PubMed
description The microscopic image analysis of pancreatic Islet of Langerhans morphology is crucial for the investigation of diabetes and metabolic diseases. Besides the general size of the islet, the percentage and relative position of glucagon-containing alpha-, and insulin-containing beta-cells is also important for pathophysiological analyses, especially in rodents. Hence, the ability to identify, quantify and spatially locate peripheral, and “involuted” alpha-cells in the islet core is an important analytical goal. There is a dearth of software available for the automated and sophisticated positional quantification of multiple cell types in the islet core. Manual analytical methods for these analyses, while relatively accurate, can suffer from a slow throughput rate as well as user-based biases. Here we describe a newly developed pancreatic islet analytical software program, Pancreas++, which facilitates the fully automated, non-biased, and highly reproducible investigation of islet area and alpha- and beta-cell quantity as well as position within the islet for either single or large batches of fluorescent images. We demonstrate the utility and accuracy of Pancreas++ by comparing its performance to other pancreatic islet size and cell type (alpha, beta) quantification methods. Our Pancreas++ analysis was significantly faster than other methods, while still retaining low error rates and a high degree of result correlation with the manually generated reference standard.
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spelling pubmed-35354212013-01-04 Pancreas++: Automated Quantification of Pancreatic Islet Cells in Microscopy Images Chen, Hongyu Martin, Bronwen Cai, Huan Fiori, Jennifer L. Egan, Josephine M. Siddiqui, Sana Maudsley, Stuart Front Physiol Physiology The microscopic image analysis of pancreatic Islet of Langerhans morphology is crucial for the investigation of diabetes and metabolic diseases. Besides the general size of the islet, the percentage and relative position of glucagon-containing alpha-, and insulin-containing beta-cells is also important for pathophysiological analyses, especially in rodents. Hence, the ability to identify, quantify and spatially locate peripheral, and “involuted” alpha-cells in the islet core is an important analytical goal. There is a dearth of software available for the automated and sophisticated positional quantification of multiple cell types in the islet core. Manual analytical methods for these analyses, while relatively accurate, can suffer from a slow throughput rate as well as user-based biases. Here we describe a newly developed pancreatic islet analytical software program, Pancreas++, which facilitates the fully automated, non-biased, and highly reproducible investigation of islet area and alpha- and beta-cell quantity as well as position within the islet for either single or large batches of fluorescent images. We demonstrate the utility and accuracy of Pancreas++ by comparing its performance to other pancreatic islet size and cell type (alpha, beta) quantification methods. Our Pancreas++ analysis was significantly faster than other methods, while still retaining low error rates and a high degree of result correlation with the manually generated reference standard. Frontiers Media S.A. 2013-01-03 /pmc/articles/PMC3535421/ /pubmed/23293605 http://dx.doi.org/10.3389/fphys.2012.00482 Text en Copyright © 2013 Chen, Martin, Cai, Fiori, Egan, Siddiqui and Maudsley. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Physiology
Chen, Hongyu
Martin, Bronwen
Cai, Huan
Fiori, Jennifer L.
Egan, Josephine M.
Siddiqui, Sana
Maudsley, Stuart
Pancreas++: Automated Quantification of Pancreatic Islet Cells in Microscopy Images
title Pancreas++: Automated Quantification of Pancreatic Islet Cells in Microscopy Images
title_full Pancreas++: Automated Quantification of Pancreatic Islet Cells in Microscopy Images
title_fullStr Pancreas++: Automated Quantification of Pancreatic Islet Cells in Microscopy Images
title_full_unstemmed Pancreas++: Automated Quantification of Pancreatic Islet Cells in Microscopy Images
title_short Pancreas++: Automated Quantification of Pancreatic Islet Cells in Microscopy Images
title_sort pancreas++: automated quantification of pancreatic islet cells in microscopy images
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3535421/
https://www.ncbi.nlm.nih.gov/pubmed/23293605
http://dx.doi.org/10.3389/fphys.2012.00482
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