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Clathrin-mediated entry and cellular localization of chlorotoxin in human glioma
BACKGROUND: Chlorotoxin (TM601), a scorpion venom- derived 36-AA peptide, is an experimental drug against recurrent glioma with tumor specificity but unknown route of intracellular distribution. The aim of this study was to evaluate the route of entry and cellular localization of TM601 in glioma cel...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3204276/ https://www.ncbi.nlm.nih.gov/pubmed/21838899 http://dx.doi.org/10.1186/1475-2867-11-27 |
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author | Wiranowska, Marzenna Colina, Lucrecia O Johnson, Joseph O |
author_facet | Wiranowska, Marzenna Colina, Lucrecia O Johnson, Joseph O |
author_sort | Wiranowska, Marzenna |
collection | PubMed |
description | BACKGROUND: Chlorotoxin (TM601), a scorpion venom- derived 36-AA peptide, is an experimental drug against recurrent glioma with tumor specificity but unknown route of intracellular distribution. The aim of this study was to evaluate the route of entry and cellular localization of TM601 in glioma cells. RESULTS: We have found that in human gliomas, lung carcinoma and normal vascular endothelial cells, TM601 localizes near trans-Golgi while in normal human dermal fibroblasts (NHDF) and astrocytes it is dispersed in the cytoplasm. The uptake of TM601 by U373 glioma cells is rapid, concentration and time dependent, not affected by inhibitors such as filipin (caveolae-dependent endocytosis) and amiloride (non-selective macropinocytosis), but significantly affected by chlorpromazine (clathrin-dependent intracellular transport of coated pits) resulting in intracellular build-up of the drug and clathrin near the Golgi. In contrast, TM601 uptake by NHDF cells was significantly affected by amiloride indicating that macropinocytosis is the dominant uptake route of TM601 in these cells. CONCLUSIONS: In conclusion, we found a distinct cellular localization pattern and uptake of TM601 by glioma cells differing from that found in normal cells. Further insight into the cellular processing of TM601 should assist in the development of effective anti-glioma therapeutic modalities. |
format | Online Article Text |
id | pubmed-3204276 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32042762011-10-30 Clathrin-mediated entry and cellular localization of chlorotoxin in human glioma Wiranowska, Marzenna Colina, Lucrecia O Johnson, Joseph O Cancer Cell Int Primary Research BACKGROUND: Chlorotoxin (TM601), a scorpion venom- derived 36-AA peptide, is an experimental drug against recurrent glioma with tumor specificity but unknown route of intracellular distribution. The aim of this study was to evaluate the route of entry and cellular localization of TM601 in glioma cells. RESULTS: We have found that in human gliomas, lung carcinoma and normal vascular endothelial cells, TM601 localizes near trans-Golgi while in normal human dermal fibroblasts (NHDF) and astrocytes it is dispersed in the cytoplasm. The uptake of TM601 by U373 glioma cells is rapid, concentration and time dependent, not affected by inhibitors such as filipin (caveolae-dependent endocytosis) and amiloride (non-selective macropinocytosis), but significantly affected by chlorpromazine (clathrin-dependent intracellular transport of coated pits) resulting in intracellular build-up of the drug and clathrin near the Golgi. In contrast, TM601 uptake by NHDF cells was significantly affected by amiloride indicating that macropinocytosis is the dominant uptake route of TM601 in these cells. CONCLUSIONS: In conclusion, we found a distinct cellular localization pattern and uptake of TM601 by glioma cells differing from that found in normal cells. Further insight into the cellular processing of TM601 should assist in the development of effective anti-glioma therapeutic modalities. BioMed Central 2011-08-12 /pmc/articles/PMC3204276/ /pubmed/21838899 http://dx.doi.org/10.1186/1475-2867-11-27 Text en Copyright ©2011 Wiranowska et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Primary Research Wiranowska, Marzenna Colina, Lucrecia O Johnson, Joseph O Clathrin-mediated entry and cellular localization of chlorotoxin in human glioma |
title | Clathrin-mediated entry and cellular localization of chlorotoxin in human glioma |
title_full | Clathrin-mediated entry and cellular localization of chlorotoxin in human glioma |
title_fullStr | Clathrin-mediated entry and cellular localization of chlorotoxin in human glioma |
title_full_unstemmed | Clathrin-mediated entry and cellular localization of chlorotoxin in human glioma |
title_short | Clathrin-mediated entry and cellular localization of chlorotoxin in human glioma |
title_sort | clathrin-mediated entry and cellular localization of chlorotoxin in human glioma |
topic | Primary Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3204276/ https://www.ncbi.nlm.nih.gov/pubmed/21838899 http://dx.doi.org/10.1186/1475-2867-11-27 |
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