Inflammation-induced brain endothelial activation leads to uptake of electrostatically stabilized iron oxide nanoparticles via sulfated glycosaminoglycans

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Item Type:	Article
Title:	Inflammation-induced brain endothelial activation leads to uptake of electrostatically stabilized iron oxide nanoparticles via sulfated glycosaminoglycans
Creators Name:	Berndt, D., Millward, J.M., Schnorr, J., Taupitz, M., Stangl, V., Paul, F., Wagner, S., Wuerfel, J.T., Sack, I., Ludwig, A. and Infante-Duarte, C.
Abstract:	Based on our previous data on the presence of very small superparamagnetic iron oxide nanoparticles (VSOP) on brain endothelial structures during experimental autoimmune encephalomyelitis (EAE), we investigated the mechanisms of VSOP binding on inflamed brain endothelial cells in vivo and in vitro. After intravenous application, VSOP were detected in brain endothelial cells of EAE animals at peak disease and prior to clinical onset. In vitro, inflammatory stimuli increased VSOP uptake by brain endothelial bEnd.3 cells, which we confirmed in primary endothelial cells and in bEnd.3 cells cultured under shear stress. Transmission electron microscopy and blocking experiments revealed that during inflammation VSOP were endocytosed by bEnd.3. Modified sulfated glycosaminoglycans (GAG) on inflamed brain endothelial cells were the primary binding site for VSOP, as GAG degradation and inhibition of GAG sulfation reduced VSOP uptake. Thus, VSOP-based MRI is sensitive to visualize early neuroinflammatory processes such as GAG modifications on brain endothelial cells.
Keywords:	Nanoparticles, Brain Endothelial Cells, Neuroinflammation, Glycosaminglycans, Extracellular Matrix, VSOP, Animals, Mice
Source:	Nanomedicine: Nanotechnology, Biology and Medicine
ISSN:	1549-9634
Publisher:	Elsevier
Volume:	13
Number:	4
Page Range:	1411-1421
Date:	May 2017
Official Publication:	https://doi.org/10.1016/j.nano.2017.01.010
PubMed:	View item in PubMed

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