ATP driven clathrin dependent entry of carbon nanospheres prefer cells with glucose receptors

<p>Abstract</p> <p>Background</p> <p>Intrinsically fluorescent glucose derived carbon nanospheres (CSP) efficiently enter mammalian cells and also cross the blood brain barrier (BBB). However, the mechanistic details of CSP entry inside mammalian cells and its specifici...

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Main Authors: Selvi Ruthrotha B, Chatterjee Snehajyoti, Jagadeesan Dinesh, Chaturbedy Piyush, Suma Bangalore, Eswaramoorthy Muthusamy, Kundu Tapas K
Format: Article
Language:English
Published: BMC 2012-08-01
Series:Journal of Nanobiotechnology
Online Access:http://www.jnanobiotechnology.com/content/10/1/35
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spelling doaj-58e9a20d88884af989c4825cb3a7d5772020-11-24T22:08:17ZengBMCJournal of Nanobiotechnology1477-31552012-08-011013510.1186/1477-3155-10-35ATP driven clathrin dependent entry of carbon nanospheres prefer cells with glucose receptorsSelvi Ruthrotha BChatterjee SnehajyotiJagadeesan DineshChaturbedy PiyushSuma BangaloreEswaramoorthy MuthusamyKundu Tapas K<p>Abstract</p> <p>Background</p> <p>Intrinsically fluorescent glucose derived carbon nanospheres (CSP) efficiently enter mammalian cells and also cross the blood brain barrier (BBB). However, the mechanistic details of CSP entry inside mammalian cells and its specificity are not known.</p> <p>Results</p> <p>In this report, the biochemical and cellular mechanism of CSP entry into the living cell have been investigated. By employing confocal imaging we show that CSP entry into the mammalian cells is an ATP-dependent clathrin mediated endocytosis process. Zeta potential studies suggest that it has a strong preference for cells which possess high levels of glucose transporters such as the glial cells, thereby enabling it to target individual organs/tissues such as the brain with increased specificity.</p> <p>Conclusion</p> <p>The endocytosis of Glucose derived CSP into mammalian cells is an ATP dependent process mediated by clathrin coated pits. CSPs utilize the surface functional groups to target cells containing glucose transporters on its membrane thereby implicating a potential application for specific targeting of the brain or cancer cells.</p> http://www.jnanobiotechnology.com/content/10/1/35
collection DOAJ
language English
format Article
sources DOAJ
author Selvi Ruthrotha B
Chatterjee Snehajyoti
Jagadeesan Dinesh
Chaturbedy Piyush
Suma Bangalore
Eswaramoorthy Muthusamy
Kundu Tapas K
spellingShingle Selvi Ruthrotha B
Chatterjee Snehajyoti
Jagadeesan Dinesh
Chaturbedy Piyush
Suma Bangalore
Eswaramoorthy Muthusamy
Kundu Tapas K
ATP driven clathrin dependent entry of carbon nanospheres prefer cells with glucose receptors
Journal of Nanobiotechnology
author_facet Selvi Ruthrotha B
Chatterjee Snehajyoti
Jagadeesan Dinesh
Chaturbedy Piyush
Suma Bangalore
Eswaramoorthy Muthusamy
Kundu Tapas K
author_sort Selvi Ruthrotha B
title ATP driven clathrin dependent entry of carbon nanospheres prefer cells with glucose receptors
title_short ATP driven clathrin dependent entry of carbon nanospheres prefer cells with glucose receptors
title_full ATP driven clathrin dependent entry of carbon nanospheres prefer cells with glucose receptors
title_fullStr ATP driven clathrin dependent entry of carbon nanospheres prefer cells with glucose receptors
title_full_unstemmed ATP driven clathrin dependent entry of carbon nanospheres prefer cells with glucose receptors
title_sort atp driven clathrin dependent entry of carbon nanospheres prefer cells with glucose receptors
publisher BMC
series Journal of Nanobiotechnology
issn 1477-3155
publishDate 2012-08-01
description <p>Abstract</p> <p>Background</p> <p>Intrinsically fluorescent glucose derived carbon nanospheres (CSP) efficiently enter mammalian cells and also cross the blood brain barrier (BBB). However, the mechanistic details of CSP entry inside mammalian cells and its specificity are not known.</p> <p>Results</p> <p>In this report, the biochemical and cellular mechanism of CSP entry into the living cell have been investigated. By employing confocal imaging we show that CSP entry into the mammalian cells is an ATP-dependent clathrin mediated endocytosis process. Zeta potential studies suggest that it has a strong preference for cells which possess high levels of glucose transporters such as the glial cells, thereby enabling it to target individual organs/tissues such as the brain with increased specificity.</p> <p>Conclusion</p> <p>The endocytosis of Glucose derived CSP into mammalian cells is an ATP dependent process mediated by clathrin coated pits. CSPs utilize the surface functional groups to target cells containing glucose transporters on its membrane thereby implicating a potential application for specific targeting of the brain or cancer cells.</p>
url http://www.jnanobiotechnology.com/content/10/1/35
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