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Pimonidazole binding in C6 rat brain glioma: relation with lipid droplet detection
In C6 rat brain glioma, we have investigated the relation between hypoxia and the presence of lipid droplets in the cytoplasm of viable cells adjacent to necrosis. For this purpose, rats were stereotaxically implanted with C6 cells. Experiments were carried out by the end of the tumour development....
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2003
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2741029/ https://www.ncbi.nlm.nih.gov/pubmed/12778075 http://dx.doi.org/10.1038/sj.bjc.6600837 |
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author | Zoula, S Rijken, P F J W Peters, J P W Farion, R Van der Sanden, B P J Van der Kogel, A J Décorps, M Rémy, C |
author_facet | Zoula, S Rijken, P F J W Peters, J P W Farion, R Van der Sanden, B P J Van der Kogel, A J Décorps, M Rémy, C |
author_sort | Zoula, S |
collection | PubMed |
description | In C6 rat brain glioma, we have investigated the relation between hypoxia and the presence of lipid droplets in the cytoplasm of viable cells adjacent to necrosis. For this purpose, rats were stereotaxically implanted with C6 cells. Experiments were carried out by the end of the tumour development. A multifluorescence staining protocol combined with digital image analysis was used to quantitatively study the spatial distribution of hypoxic cells (pimonidazole), blood perfusion (Hoechst 33342), total vascular bed (collagen type IV) and lipid droplets (Red Oil) in single frozen sections. All tumours (n=6) showed necrosis, pimonidazole binding and lipid droplets. Pimonidazole binding occurred at a mean distance of 114 μm from perfused vessels mainly around necrosis. Lipid droplets were principally located in the necrotic tissue. Some smaller droplets were also observed in part of the pimonidazole-binding cells surrounding necrosis. Hence, lipid droplets appeared only in hypoxic cells adjacent to necrosis, at an approximate distance of 181 μm from perfused vessels. In conclusion, our results show that severe hypoxic cells accumulated small lipid droplets. However, a 100% colocalisation of hypoxia and lipid droplets does not exist. Thus, lipid droplets cannot be considered as a surrogate marker of hypoxia, but rather of severe, prenecrotic hypoxia. |
format | Text |
id | pubmed-2741029 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-27410292009-09-10 Pimonidazole binding in C6 rat brain glioma: relation with lipid droplet detection Zoula, S Rijken, P F J W Peters, J P W Farion, R Van der Sanden, B P J Van der Kogel, A J Décorps, M Rémy, C Br J Cancer Experimental Therapeutics In C6 rat brain glioma, we have investigated the relation between hypoxia and the presence of lipid droplets in the cytoplasm of viable cells adjacent to necrosis. For this purpose, rats were stereotaxically implanted with C6 cells. Experiments were carried out by the end of the tumour development. A multifluorescence staining protocol combined with digital image analysis was used to quantitatively study the spatial distribution of hypoxic cells (pimonidazole), blood perfusion (Hoechst 33342), total vascular bed (collagen type IV) and lipid droplets (Red Oil) in single frozen sections. All tumours (n=6) showed necrosis, pimonidazole binding and lipid droplets. Pimonidazole binding occurred at a mean distance of 114 μm from perfused vessels mainly around necrosis. Lipid droplets were principally located in the necrotic tissue. Some smaller droplets were also observed in part of the pimonidazole-binding cells surrounding necrosis. Hence, lipid droplets appeared only in hypoxic cells adjacent to necrosis, at an approximate distance of 181 μm from perfused vessels. In conclusion, our results show that severe hypoxic cells accumulated small lipid droplets. However, a 100% colocalisation of hypoxia and lipid droplets does not exist. Thus, lipid droplets cannot be considered as a surrogate marker of hypoxia, but rather of severe, prenecrotic hypoxia. Nature Publishing Group 2003-05-06 2003-04-29 /pmc/articles/PMC2741029/ /pubmed/12778075 http://dx.doi.org/10.1038/sj.bjc.6600837 Text en Copyright © 2003 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 Zoula, S Rijken, P F J W Peters, J P W Farion, R Van der Sanden, B P J Van der Kogel, A J Décorps, M Rémy, C Pimonidazole binding in C6 rat brain glioma: relation with lipid droplet detection |
title | Pimonidazole binding in C6 rat brain glioma: relation with lipid droplet detection |
title_full | Pimonidazole binding in C6 rat brain glioma: relation with lipid droplet detection |
title_fullStr | Pimonidazole binding in C6 rat brain glioma: relation with lipid droplet detection |
title_full_unstemmed | Pimonidazole binding in C6 rat brain glioma: relation with lipid droplet detection |
title_short | Pimonidazole binding in C6 rat brain glioma: relation with lipid droplet detection |
title_sort | pimonidazole binding in c6 rat brain glioma: relation with lipid droplet detection |
topic | Experimental Therapeutics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2741029/ https://www.ncbi.nlm.nih.gov/pubmed/12778075 http://dx.doi.org/10.1038/sj.bjc.6600837 |
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