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Apoptosis is associated with triacylglycerol accumulation in Jurkat T-cells

Magnetic resonance spectroscopy is increasingly used as a non-invasive method to investigate apoptosis. Apoptosis was induced in Jurkat T-cells by Fas mAb. (1)H magnetic resonance spectra of live cells showed an increase in methylene signal as well as methylene/methyl ratio of fatty acid side chains...

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Autores principales: Al-Saffar, N M S, Titley, J C, Robertson, D, Clarke, P A, Jackson, L E, Leach, M O, Ronen, S M
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364152/
https://www.ncbi.nlm.nih.gov/pubmed/11953830
http://dx.doi.org/10.1038/sj.bjc.6600188
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author Al-Saffar, N M S
Titley, J C
Robertson, D
Clarke, P A
Jackson, L E
Leach, M O
Ronen, S M
author_facet Al-Saffar, N M S
Titley, J C
Robertson, D
Clarke, P A
Jackson, L E
Leach, M O
Ronen, S M
author_sort Al-Saffar, N M S
collection PubMed
description Magnetic resonance spectroscopy is increasingly used as a non-invasive method to investigate apoptosis. Apoptosis was induced in Jurkat T-cells by Fas mAb. (1)H magnetic resonance spectra of live cells showed an increase in methylene signal as well as methylene/methyl ratio of fatty acid side chains at 5 and 24 h following induction of apoptosis. To explain this observation, (1)H magnetic resonance spectra of cell extracts were investigated. These demonstrated a 70.0±7.0%, 114.0±8.0% and 90.0±5.0% increase in the concentration of triacylglycerols following 3, 5 and 7 h of Fas mAb treatment (P<0.05). Confocal microscopy images of cells stained with the lipophilic dye Nile Red demonstrated the presence of lipid droplets in the cell cytoplasm. Quantification of the stained lipids by flow cytometry showed a good correlation with the magnetic resonance results (P⩾0.05 at 3, 5 and 7 h). (31)P magnetic resonance spectra showed a drop in phosphatidylcholine content of apoptosing cells, indicating that alteration in phosphatidylcholine metabolism could be the source of triacylglycerol accumulation during apoptosis. In summary, apoptosis is associated with an early accumulation of mobile triacylglycerols mostly in the form of cytoplasmic lipid droplets. This is reflected in an increase in the methylene/methyl ratio which could be detected by magnetic resonance spectroscopy. British Journal of Cancer (2002) 86, 963–970. DOI: 10.1038/sj/bjc/6600188 www.bjcancer.com © 2002 Cancer Research UK
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spelling pubmed-23641522009-09-10 Apoptosis is associated with triacylglycerol accumulation in Jurkat T-cells Al-Saffar, N M S Titley, J C Robertson, D Clarke, P A Jackson, L E Leach, M O Ronen, S M Br J Cancer Experimental Therapeutics Magnetic resonance spectroscopy is increasingly used as a non-invasive method to investigate apoptosis. Apoptosis was induced in Jurkat T-cells by Fas mAb. (1)H magnetic resonance spectra of live cells showed an increase in methylene signal as well as methylene/methyl ratio of fatty acid side chains at 5 and 24 h following induction of apoptosis. To explain this observation, (1)H magnetic resonance spectra of cell extracts were investigated. These demonstrated a 70.0±7.0%, 114.0±8.0% and 90.0±5.0% increase in the concentration of triacylglycerols following 3, 5 and 7 h of Fas mAb treatment (P<0.05). Confocal microscopy images of cells stained with the lipophilic dye Nile Red demonstrated the presence of lipid droplets in the cell cytoplasm. Quantification of the stained lipids by flow cytometry showed a good correlation with the magnetic resonance results (P⩾0.05 at 3, 5 and 7 h). (31)P magnetic resonance spectra showed a drop in phosphatidylcholine content of apoptosing cells, indicating that alteration in phosphatidylcholine metabolism could be the source of triacylglycerol accumulation during apoptosis. In summary, apoptosis is associated with an early accumulation of mobile triacylglycerols mostly in the form of cytoplasmic lipid droplets. This is reflected in an increase in the methylene/methyl ratio which could be detected by magnetic resonance spectroscopy. British Journal of Cancer (2002) 86, 963–970. DOI: 10.1038/sj/bjc/6600188 www.bjcancer.com © 2002 Cancer Research UK Nature Publishing Group 2002-03-18 /pmc/articles/PMC2364152/ /pubmed/11953830 http://dx.doi.org/10.1038/sj.bjc.6600188 Text en Copyright © 2002 Cancer Research UK https://creativecommons.org/licenses/by/4.0/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 https://creativecommons.org/licenses/by/4.0/.
spellingShingle Experimental Therapeutics
Al-Saffar, N M S
Titley, J C
Robertson, D
Clarke, P A
Jackson, L E
Leach, M O
Ronen, S M
Apoptosis is associated with triacylglycerol accumulation in Jurkat T-cells
title Apoptosis is associated with triacylglycerol accumulation in Jurkat T-cells
title_full Apoptosis is associated with triacylglycerol accumulation in Jurkat T-cells
title_fullStr Apoptosis is associated with triacylglycerol accumulation in Jurkat T-cells
title_full_unstemmed Apoptosis is associated with triacylglycerol accumulation in Jurkat T-cells
title_short Apoptosis is associated with triacylglycerol accumulation in Jurkat T-cells
title_sort apoptosis is associated with triacylglycerol accumulation in jurkat t-cells
topic Experimental Therapeutics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364152/
https://www.ncbi.nlm.nih.gov/pubmed/11953830
http://dx.doi.org/10.1038/sj.bjc.6600188
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