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Updated: Oct 13, 2026

Identification and Isolation of Slow-Dividing Cells in Human Glioblastoma Using Carboxy Fluorescein Succinimidyl Ester (CFSE)
Published on: April 29, 2012
Fast blue, a fluorescent tracer in glioma cell culture, affects cell proliferation and motility
G H Vince1, H Bouterfa, R Goldbrunner
1Department of Neurosurgery, University of Würzburg, Germany. nch-tumorbiology@mail.uni-wuerzburg.de
Abstract:
The azo-dye, Fast Blue (FB), initially employed for retrograde neuronal tracing is increasingly used in cell invasion and migration studies to detect living cells in monolayer and glioma tumor cell spheroid models. As yet, it is assumed that a cell stained with a tracker dye retains the characteristics of the original cell. The following experiments compared the adhesion, migration and proliferation properties of the cell lines U373 and GaMG with and without FB staining. FB staining reduced cell adhesion (P < 0.01) and proliferative activity (P < 0.01) and also had a significant inhibitory effect on cell migration (P < 0.001). From the results presented it follows that FB staining markedly influences basic cell characteristics.

