Structural and elemental changes in glioblastoma cells in situ: complementary imaging with high resolution visible light- and X-ray microscopyElectronic supplementary information (ESI) available. See DOI: 10.1039/c6an02532c

The glioblastoma (GBM) is characterized by a short median survival and an almost 100% tumor related mortality. GBM cells exhibit highly invasive behavior whose mechanisms are not yet fully understood. The present study explores application of X-ray and visible light microscopy to display the element...

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Hauptverfasser: Du i, Tanja, Paunesku, Tatjana, Chen, Si, Ninkovi, Milena, Speling, Swetlana, Wilke, Charlene, Lai, Barry, Woloschak, Gayle
Format: Artikel
Sprache:eng
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Zusammenfassung:The glioblastoma (GBM) is characterized by a short median survival and an almost 100% tumor related mortality. GBM cells exhibit highly invasive behavior whose mechanisms are not yet fully understood. The present study explores application of X-ray and visible light microscopy to display the elemental and structural images of cells from 3 patient derived GMB samples and an established GMB cell line. Slight differences in elemental concentrations, in actin cytoskeleton organization and cell morphology were noted between all cells types by X-ray fluorescence and full field soft X-ray microscopy, as well as the Structured Illumination Super-resolution Microscope (SIM). Different sample preparation approaches were used to match each imaging technique. While preparation for SIM included cell fixation and staining, intact frozen hydrated cells were used for the trace element imaging by hard X-ray fluorescence and exploration of the structural features by soft X-ray absorption tomography. Each technique documented differences between samples with regard to morphology and elemental composition and underscored the importance of use of multiple patient derived samples for detailed GBM study. The study explores application of X-ray and high resolution visible light microscopy to investigate the elemental and structural changes in cells from 3 patient derived glioblastoma samples.
ISSN:0003-2654
1364-5528
DOI:10.1039/c6an02532c