Clathrin-mediated entry and cellular localization of chlorotoxin in human glioma

<p>Abstract</p> <p>Background</p> <p>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...

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Main Authors: Johnson Joseph O, Colina Lucrecia O, Wiranowska Marzenna
Format: Article
Language:English
Published: BMC 2011-08-01
Series:Cancer Cell International
Online Access:http://www.cancerci.com/content/11/1/27
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spelling doaj-5ee4aa3885ac49d29af5277f100a34922020-11-25T02:43:58ZengBMCCancer Cell International1475-28672011-08-011112710.1186/1475-2867-11-27Clathrin-mediated entry and cellular localization of chlorotoxin in human gliomaJohnson Joseph OColina Lucrecia OWiranowska Marzenna<p>Abstract</p> <p>Background</p> <p>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.</p> <p>Results</p> <p>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.</p> <p>Conclusions</p> <p>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.</p> http://www.cancerci.com/content/11/1/27
collection DOAJ
language English
format Article
sources DOAJ
author Johnson Joseph O
Colina Lucrecia O
Wiranowska Marzenna
spellingShingle Johnson Joseph O
Colina Lucrecia O
Wiranowska Marzenna
Clathrin-mediated entry and cellular localization of chlorotoxin in human glioma
Cancer Cell International
author_facet Johnson Joseph O
Colina Lucrecia O
Wiranowska Marzenna
author_sort Johnson Joseph O
title 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_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_sort clathrin-mediated entry and cellular localization of chlorotoxin in human glioma
publisher BMC
series Cancer Cell International
issn 1475-2867
publishDate 2011-08-01
description <p>Abstract</p> <p>Background</p> <p>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.</p> <p>Results</p> <p>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.</p> <p>Conclusions</p> <p>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.</p>
url http://www.cancerci.com/content/11/1/27
work_keys_str_mv AT johnsonjosepho clathrinmediatedentryandcellularlocalizationofchlorotoxininhumanglioma
AT colinalucreciao clathrinmediatedentryandcellularlocalizationofchlorotoxininhumanglioma
AT wiranowskamarzenna clathrinmediatedentryandcellularlocalizationofchlorotoxininhumanglioma
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