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Efficacy of ImageJ in the assessment of apoptosis

OBJECTIVE: To verify the efficacy of ImageJ 1.43 n in determining the extent of apoptosis which is a complex and multistep process. STUDY DESIGN: Cisplatin in different concentrations was used to induce apoptosis in cultured Hep2 cells. Cell viability assay and nuclear image analysis of stained Hep2...

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Autores principales: Helmy, Iman M, Abdel Azim, Adel M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3307432/
https://www.ncbi.nlm.nih.gov/pubmed/22309648
http://dx.doi.org/10.1186/1746-1596-7-15
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author Helmy, Iman M
Abdel Azim, Adel M
author_facet Helmy, Iman M
Abdel Azim, Adel M
author_sort Helmy, Iman M
collection PubMed
description OBJECTIVE: To verify the efficacy of ImageJ 1.43 n in determining the extent of apoptosis which is a complex and multistep process. STUDY DESIGN: 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. RESULTS: 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. CONCLUSION: 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. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/5929043086367338
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spelling pubmed-33074322012-03-20 Efficacy of ImageJ in the assessment of apoptosis Helmy, Iman M Abdel Azim, Adel M Diagn Pathol Research OBJECTIVE: To verify the efficacy of ImageJ 1.43 n in determining the extent of apoptosis which is a complex and multistep process. STUDY DESIGN: 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. RESULTS: 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. CONCLUSION: 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. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/5929043086367338 BioMed Central 2012-02-06 /pmc/articles/PMC3307432/ /pubmed/22309648 http://dx.doi.org/10.1186/1746-1596-7-15 Text en Copyright ©2012 Helmy and Abdel Azim; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Helmy, Iman M
Abdel Azim, Adel M
Efficacy of ImageJ in the assessment of apoptosis
title 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_short Efficacy of ImageJ in the assessment of apoptosis
title_sort efficacy of imagej in the assessment of apoptosis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3307432/
https://www.ncbi.nlm.nih.gov/pubmed/22309648
http://dx.doi.org/10.1186/1746-1596-7-15
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