Nestin expression in the cell lines derived from glioblastoma multiforme

被引:66
作者
Veselska, R [1 ]
Kuglik, P
Cejpek, P
Svachova, H
Neradil, J
Loja, T
Relichova, J
机构
[1] Masaryk Univ, Sch Med, Dept Biol, Cell Culture Lab, Brno, Czech Republic
[2] Masaryk Univ, Sch Sci, Dept Genet & Mol Biol, Lab Mol Cytogenet, Brno, Czech Republic
[3] Masaryk Univ, Sch Med, Dept Neurosurg, Brno, Czech Republic
关键词
D O I
10.1186/1471-2407-6-32
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Nestin is a protein belonging to class VI of intermediate filaments that is produced in stem/progenitor cells in the mammalian CNS during development and is consecutively replaced by other intermediate filament proteins (neurofilaments, GFAP). Down-regulated nestin may be reexpressed in the adult organism under certain pathological conditions ( brain injury, ischemia, inflammation, neoplastic transformation). Our work focused on a detailed study of the nestin cytoskeleton in cell lines derived from glioblastoma multiforme, because re-expression of nestin together with down-regulation of GFAP has been previously reported in this type of brain tumor. Methods: Two cell lines were derived from the tumor tissue of patients treated for glioblastoma multiforme. Nestin and other cytoskeletal proteins were visualized using imunocytochemical methods: indirect immunofluorescence and immunogold- labelling. Results: Using epifluorescence and confocal microscopy, we described the morphology of nestin-positive intermediate filaments in glioblastoma cells of both primary cultures and the derived cell lines, as well as the reorganization of nestin during mitosis. Our most important result came through transmission electron microscopy and provided clear evidence that nestin is present in the cell nucleus. Conclusion: Detailed information concerning the pattern of the nestin cytoskeleton in glioblastoma cell lines and especially the demonstration of nestin in the nucleus represent an important background for further studies of nestin re-expression in relationship to tumor malignancy and invasive potential.
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页数:12
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