Manufactured aluminum oxide nanoparticles decrease expression of tight junction proteins in brain vasculature

Lei Chen, Robert A. Yokel, Bernhard Hennig, Michal Toborek

Research output: Contribution to journalArticlepeer-review

148 Scopus citations

Abstract

Manufactured nanoparticles of aluminum oxide (nano-alumina) have been widely used in the environment; however, their potential toxicity provides a growing concern for human health. The present study focuses on the hypothesis that nano-alumina can affect the blood-brain barrier and induce endothelial toxicity. In the first series of experiments, human brain microvascular endothelial cells (HBMEC) were exposed to alumina and control nanoparticles in dose- and time-responsive manners. Treatment with nano-alumina markedly reduced HBMEC viability, altered mitochondrial potential, increased cellular oxidation, and decreased tight junction protein expression as compared to control nanoparticles. Alterations of tight junction protein levels were prevented by cellular enrichment with glutathione. In the second series of experiments, rats were infused with nano-alumina at the dose of 29 mg/kg and the brains were stained for expression of tight junction proteins. Treatment with nano-alumina resulted in a marked fragmentation and disruption of integrity of claudin-5 and occludin. These results indicate that cerebral vasculature can be affected by nano-alumina. In addition, our data indicate that alterations of mitochondrial functions may be the underlying mechanism of nano-alumina toxicity.

Original languageEnglish (US)
Pages (from-to)286-295
Number of pages10
JournalJournal of Neuroimmune Pharmacology
Volume3
Issue number4
DOIs
StatePublished - Dec 2008

Keywords

  • Blood-brain barrier
  • Manufactured nanoparticles
  • Nano-alumina
  • Tight junctions

ASJC Scopus subject areas

  • Pharmacology
  • Immunology and Allergy
  • Immunology
  • Neuroscience (miscellaneous)

Fingerprint Dive into the research topics of 'Manufactured aluminum oxide nanoparticles decrease expression of tight junction proteins in brain vasculature'. Together they form a unique fingerprint.

Cite this