Pimonidazole binding in C6 rat brain glioma: relation with lipid droplet detection

被引:0
|
作者
S Zoula
P F J W Rijken
J P W Peters
R Farion
B P J Van der Sanden
A J Van der Kogel
M Décorps
C Rémy
机构
[1] Laboratoire Mixte INSERM U438 ‘RMN Bioclinique’,Department of Radiotherapy
[2] Université Joseph Fourier,undefined
[3] Laboratoire Correspondent de CEA,undefined
[4] Centre Hospitalier Universitaire Pavillon B,undefined
[5] University of Nijmegen,undefined
来源
British Journal of Cancer | 2003年 / 88卷
关键词
glioma; hypoxia; lipid droplets; perfusion; image analysis;
D O I
暂无
中图分类号
学科分类号
摘要
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.
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页码:1439 / 1444
页数:5
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