Abstract |
The objective of the present study was to evaluate the influence of 2,4,6-tribromophenyl isocyanate (TBPI) on the cellular and nuclear uptake of the fluorescein isothiocyanate ( FITC) labeled SV 40 T antigen nuclear localization sequence in human LN18 and U373 glioma cells. Therefore, the FITC-labeled nuclear localization sequence (NLS) of the SV 40 T antigen was coupled to 2,4,6-TBPI. This TBPI-NLS conjugate was taken up by the cell nuclei of more than 90% of human malignant glioma cells. The nuclearly stained cells showed clear signs of cell death. However only up to 10% of the cells were stained after incubation with the TBPI-lacking NLS of the SV 40 T antigen together with free, unbound TBPI. These cells stayed alive. TBPI, when bound to small peptides, may be an important component for future drugs against gliomas.
|
Authors | Stefan Heckl, Alexander Sturzu, Alireza Gharabaghi, Hartmut Echner, Thomas Nagele |
Journal | European journal of pharmacology
(Eur J Pharmacol)
Vol. 583
Issue 1
Pg. 32-6
(Mar 31 2008)
ISSN: 0014-2999 [Print] Netherlands |
PMID | 18262518
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Chemical References |
- 2,4,6-tribromophenyl isocyanate
- Antigens, Polyomavirus Transforming
- Fluorescent Dyes
- Isocyanates
- Fluorescein-5-isothiocyanate
|
Topics |
- Antigens, Polyomavirus Transforming
(metabolism)
- Biological Transport, Active
- Brain Neoplasms
(metabolism)
- Cell Line, Tumor
- Cell Nucleus
(metabolism, ultrastructure)
- Flow Cytometry
- Fluorescein-5-isothiocyanate
- Fluorescent Dyes
- Glioma
(metabolism)
- Humans
- Isocyanates
(pharmacology)
- Microscopy, Confocal
- Spectrometry, Mass, Electrospray Ionization
|