Efficacy of ImageJ in the assessment of apoptosis

<p>Abstract</p> <p>Objective</p> <p>To verify the efficacy of ImageJ 1.43 n in determining the extent of apoptosis which is a complex and multistep process.</p> <p>Study Design</p> <p>Cisplatin in different concentrations was used to induce apopt...

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Main Authors: Helmy Iman M, Abdel Azim Adel M
Format: Article
Language:English
Published: BMC 2012-02-01
Series:Diagnostic Pathology
Subjects:
Online Access:http://www.diagnosticpathology.org/content/7/1/15
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spelling doaj-d53dc60ae43b4740b68126767b15354b2020-11-24T21:57:43ZengBMCDiagnostic Pathology1746-15962012-02-01711510.1186/1746-1596-7-15Efficacy of ImageJ in the assessment of apoptosisHelmy Iman MAbdel Azim Adel M<p>Abstract</p> <p>Objective</p> <p>To verify the efficacy of ImageJ 1.43 n in determining the extent of apoptosis which is a complex and multistep process.</p> <p>Study Design</p> <p>Cisplatin in different concentrations was used to induce apoptosis in cultured Hep2 cells. Cell viability assay and nuclear image analysis of stained Hep2 cells were used to discriminate apoptotic cells and cells suspected to be undergoing apoptosis from control cells based on parameters such as nuclear area, circularity, perimeter and nuclear area factor (NAF), in association with visual morphology.</p> <p>Results</p> <p>Image analysis revealed a progressive and highly significant decrease in nuclear area factor detected in apoptotic cells and in cells suspected of undergoing apoptosis compared to the control cells (P-values < 0.01). Some of the other studied parameters showed also the same trend. This decrease was assumed to indicate DNA loss. Image analysis results correlated positively and significantly with the results obtained by cell viability assay (R = 0.958, P-value = 0.042). NAF was the most reliable parameter in assessment of apoptosis.</p> <p>Conclusion</p> <p>Nuclear area factor can be calculated using powerful free and open-source software. Consequently, a quantitative measure of apoptosis can be obtained that is linked to morphological changes. ImageJ 1.43 n may therefore provide a useful tool for the assessment and discrimination of apoptotic cells.</p> <p>Virtual slides</p> <p>The virtual slide(s) for this article can be found here:</p> <p><url>http://www.diagnosticpathology.diagnomx.eu/vs/5929043086367338</url></p> http://www.diagnosticpathology.org/content/7/1/15ApoptosisHep2 cellImage analysisNAF (nuclear area factor)
collection DOAJ
language English
format Article
sources DOAJ
author Helmy Iman M
Abdel Azim Adel M
spellingShingle Helmy Iman M
Abdel Azim Adel M
Efficacy of ImageJ in the assessment of apoptosis
Diagnostic Pathology
Apoptosis
Hep2 cell
Image analysis
NAF (nuclear area factor)
author_facet Helmy Iman M
Abdel Azim Adel M
author_sort Helmy Iman M
title Efficacy of ImageJ in the assessment of apoptosis
title_short Efficacy of ImageJ in the assessment of apoptosis
title_full Efficacy of ImageJ in the assessment of apoptosis
title_fullStr Efficacy of ImageJ in the assessment of apoptosis
title_full_unstemmed Efficacy of ImageJ in the assessment of apoptosis
title_sort efficacy of imagej in the assessment of apoptosis
publisher BMC
series Diagnostic Pathology
issn 1746-1596
publishDate 2012-02-01
description <p>Abstract</p> <p>Objective</p> <p>To verify the efficacy of ImageJ 1.43 n in determining the extent of apoptosis which is a complex and multistep process.</p> <p>Study Design</p> <p>Cisplatin in different concentrations was used to induce apoptosis in cultured Hep2 cells. Cell viability assay and nuclear image analysis of stained Hep2 cells were used to discriminate apoptotic cells and cells suspected to be undergoing apoptosis from control cells based on parameters such as nuclear area, circularity, perimeter and nuclear area factor (NAF), in association with visual morphology.</p> <p>Results</p> <p>Image analysis revealed a progressive and highly significant decrease in nuclear area factor detected in apoptotic cells and in cells suspected of undergoing apoptosis compared to the control cells (P-values < 0.01). Some of the other studied parameters showed also the same trend. This decrease was assumed to indicate DNA loss. Image analysis results correlated positively and significantly with the results obtained by cell viability assay (R = 0.958, P-value = 0.042). NAF was the most reliable parameter in assessment of apoptosis.</p> <p>Conclusion</p> <p>Nuclear area factor can be calculated using powerful free and open-source software. Consequently, a quantitative measure of apoptosis can be obtained that is linked to morphological changes. ImageJ 1.43 n may therefore provide a useful tool for the assessment and discrimination of apoptotic cells.</p> <p>Virtual slides</p> <p>The virtual slide(s) for this article can be found here:</p> <p><url>http://www.diagnosticpathology.diagnomx.eu/vs/5929043086367338</url></p>
topic Apoptosis
Hep2 cell
Image analysis
NAF (nuclear area factor)
url http://www.diagnosticpathology.org/content/7/1/15
work_keys_str_mv AT helmyimanm efficacyofimagejintheassessmentofapoptosis
AT abdelazimadelm efficacyofimagejintheassessmentofapoptosis
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