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Effects of Fullerenols on Mouse Brain Microvascular Endothelial Cells

Fullerenols, water-soluble C60-fullerene derivatives, have been shown to exert neuroprotective effects in vitro and in vivo, most likely due to their capability to scavenge free radicals. However, little is known about the effects of fullerenols on the blood–brain barrier (BBB), especially on cerebr...

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Detalles Bibliográficos
Autores principales: Schuhmann, Michael K., Fluri, Felix
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5578172/
https://www.ncbi.nlm.nih.gov/pubmed/28817067
http://dx.doi.org/10.3390/ijms18081783
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author Schuhmann, Michael K.
Fluri, Felix
author_facet Schuhmann, Michael K.
Fluri, Felix
author_sort Schuhmann, Michael K.
collection PubMed
description Fullerenols, water-soluble C60-fullerene derivatives, have been shown to exert neuroprotective effects in vitro and in vivo, most likely due to their capability to scavenge free radicals. However, little is known about the effects of fullerenols on the blood–brain barrier (BBB), especially on cerebral endothelial cells under inflammatory conditions. Here, we investigated whether the treatment of primary mouse brain microvascular endothelial cells with fullerenols impacts basal and inflammatory blood–brain barrier (BBB) properties in vitro. While fullerenols (1, 10, and 100 µg/mL) did not change transendothelial electrical resistance under basal and inflammatory conditions, 100 µg/mL of fullerenol significantly reduced erk1/2 activation and resulted in an activation of NFκB in an inflammatory milieu. Our findings suggest that fullerenols might counteract oxidative stress via the erk1/2 and NFκB pathways, and thus are able to protect microvascular endothelial cells under inflammatory conditions.
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spelling pubmed-55781722017-09-05 Effects of Fullerenols on Mouse Brain Microvascular Endothelial Cells Schuhmann, Michael K. Fluri, Felix Int J Mol Sci Article Fullerenols, water-soluble C60-fullerene derivatives, have been shown to exert neuroprotective effects in vitro and in vivo, most likely due to their capability to scavenge free radicals. However, little is known about the effects of fullerenols on the blood–brain barrier (BBB), especially on cerebral endothelial cells under inflammatory conditions. Here, we investigated whether the treatment of primary mouse brain microvascular endothelial cells with fullerenols impacts basal and inflammatory blood–brain barrier (BBB) properties in vitro. While fullerenols (1, 10, and 100 µg/mL) did not change transendothelial electrical resistance under basal and inflammatory conditions, 100 µg/mL of fullerenol significantly reduced erk1/2 activation and resulted in an activation of NFκB in an inflammatory milieu. Our findings suggest that fullerenols might counteract oxidative stress via the erk1/2 and NFκB pathways, and thus are able to protect microvascular endothelial cells under inflammatory conditions. MDPI 2017-08-17 /pmc/articles/PMC5578172/ /pubmed/28817067 http://dx.doi.org/10.3390/ijms18081783 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Schuhmann, Michael K.
Fluri, Felix
Effects of Fullerenols on Mouse Brain Microvascular Endothelial Cells
title Effects of Fullerenols on Mouse Brain Microvascular Endothelial Cells
title_full Effects of Fullerenols on Mouse Brain Microvascular Endothelial Cells
title_fullStr Effects of Fullerenols on Mouse Brain Microvascular Endothelial Cells
title_full_unstemmed Effects of Fullerenols on Mouse Brain Microvascular Endothelial Cells
title_short Effects of Fullerenols on Mouse Brain Microvascular Endothelial Cells
title_sort effects of fullerenols on mouse brain microvascular endothelial cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5578172/
https://www.ncbi.nlm.nih.gov/pubmed/28817067
http://dx.doi.org/10.3390/ijms18081783
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