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  The glycocalyx regulates the uptake of nanoparticles by human endothelial cells in vitro

Möckl, L., Hirn, S., Torrano, A. A., Uhl, B., Braeuchle, C., & Krombach, F. (2017). The glycocalyx regulates the uptake of nanoparticles by human endothelial cells in vitro. Nanomedicine, 12(3), 207-217. doi:10.2217/nnm-2016-0332.

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 Creators:
Möckl, Leonhard1, 2, Author           
Hirn, Stephanie2, Author
Torrano, Adriano A.2, Author
Uhl, Bernd2, Author
Braeuchle, Christoph2, Author
Krombach, Fritz2, Author
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1External Organizations, ou_persistent22              
2Ludwig-Maximilians-Universität München, ou_persistent22              

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Free keywords: endothelial cells; glycocalyx; heparan sulfate; live-cell imaging; nanoparticleendothelium interactions; nanoparticles; polystyrene nanospheres
 Abstract: Aim: To assess the role of the endothelial glycocalyx (eGCX) for the uptake of nanoparticles by endothelial cells. Methods: The expression of the eGCX on cultured human umbilical vein endothelial cells was determined by immunostaining of heparan sulfate. Enzymatic degradation of the eGCX was achieved by incubating the cells with eGCX-shedding enzymes. The uptake of 50-nm polystyrene nanospheres was quantified by confocal microscopy. Results: Human umbilical vein endothelial cells expressed a robust eGCX when cultured for 10 days. The uptake of both carboxylated and aminated polystyrene nanospheres was significantly increased in cells in which the glycocalyx was enzymatically degraded, while it remained at a low level in cells with an intact glycocalyx. Conclusion: The eGCX constitutes a barrier against the internalization of blood-borne nanoparticles by endothelial cells.

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Language(s): eng - English
 Dates: 2017-02
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: ISI: 000395674900007
DOI: 10.2217/nnm-2016-0332
 Degree: -

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Title: Nanomedicine
Source Genre: Journal
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Publ. Info: Future Medicine Ltd
Pages: - Volume / Issue: 12 (3) Sequence Number: - Start / End Page: 207 - 217 Identifier: ISSN: 1743-5889
CoNE: https://pure.mpg.de/cone/journals/resource/1743-5889