Iron oxide nanoparticles induce human microvascular endothelial cell permeability through reactive oxygen species production and microtubule remodeling
<p>Abstract</p> <p>Background</p> <p>Engineered iron nanoparticles are being explored for the development of biomedical applications and many other industry purposes. However, to date little is known concerning the precise mechanisms of translocation of iron nanoparticl...
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doaj-1782a4ddb45f40d698ffcc920a4d30682020-11-24T20:51:11ZengBMCParticle and Fibre Toxicology1743-89772009-01-0161110.1186/1743-8977-6-1Iron oxide nanoparticles induce human microvascular endothelial cell permeability through reactive oxygen species production and microtubule remodelingShi XianglinPorter DalePacurari MaricicaSchwegler-Berry DianeGuo NancyShao RongQian YongApopa Patrick LVallyathan ValCastranova VincentFlynn Daniel C<p>Abstract</p> <p>Background</p> <p>Engineered iron nanoparticles are being explored for the development of biomedical applications and many other industry purposes. However, to date little is known concerning the precise mechanisms of translocation of iron nanoparticles into targeted tissues and organs from blood circulation, as well as the underlying implications of potential harmful health effects in human.</p> <p>Results</p> <p>The confocal microscopy imaging analysis demonstrates that exposure to engineered iron nanoparticles induces an increase in cell permeability in human microvascular endothelial cells. Our studies further reveal iron nanoparticles enhance the permeability through the production of reactive oxygen species (ROS) and the stabilization of microtubules. We also showed Akt/GSK-3β signaling pathways are involved in iron nanoparticle-induced cell permeability. The inhibition of ROS demonstrate ROS play a major role in regulating Akt/GSK-3β – mediated cell permeability upon iron nanoparticle exposure. These results provide new insights into the bioreactivity of engineered iron nanoparticles which can inform potential applications in medical imaging or drug delivery.</p> <p>Conclusion</p> <p>Our results indicate that exposure to iron nanoparticles induces an increase in endothelial cell permeability through ROS oxidative stress-modulated microtubule remodeling. The findings from this study provide new understandings on the effects of nanoparticles on vascular transport of macromolecules and drugs.</p> http://www.particleandfibretoxicology.com/content/6/1/1 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Shi Xianglin Porter Dale Pacurari Maricica Schwegler-Berry Diane Guo Nancy Shao Rong Qian Yong Apopa Patrick L Vallyathan Val Castranova Vincent Flynn Daniel C |
spellingShingle |
Shi Xianglin Porter Dale Pacurari Maricica Schwegler-Berry Diane Guo Nancy Shao Rong Qian Yong Apopa Patrick L Vallyathan Val Castranova Vincent Flynn Daniel C Iron oxide nanoparticles induce human microvascular endothelial cell permeability through reactive oxygen species production and microtubule remodeling Particle and Fibre Toxicology |
author_facet |
Shi Xianglin Porter Dale Pacurari Maricica Schwegler-Berry Diane Guo Nancy Shao Rong Qian Yong Apopa Patrick L Vallyathan Val Castranova Vincent Flynn Daniel C |
author_sort |
Shi Xianglin |
title |
Iron oxide nanoparticles induce human microvascular endothelial cell permeability through reactive oxygen species production and microtubule remodeling |
title_short |
Iron oxide nanoparticles induce human microvascular endothelial cell permeability through reactive oxygen species production and microtubule remodeling |
title_full |
Iron oxide nanoparticles induce human microvascular endothelial cell permeability through reactive oxygen species production and microtubule remodeling |
title_fullStr |
Iron oxide nanoparticles induce human microvascular endothelial cell permeability through reactive oxygen species production and microtubule remodeling |
title_full_unstemmed |
Iron oxide nanoparticles induce human microvascular endothelial cell permeability through reactive oxygen species production and microtubule remodeling |
title_sort |
iron oxide nanoparticles induce human microvascular endothelial cell permeability through reactive oxygen species production and microtubule remodeling |
publisher |
BMC |
series |
Particle and Fibre Toxicology |
issn |
1743-8977 |
publishDate |
2009-01-01 |
description |
<p>Abstract</p> <p>Background</p> <p>Engineered iron nanoparticles are being explored for the development of biomedical applications and many other industry purposes. However, to date little is known concerning the precise mechanisms of translocation of iron nanoparticles into targeted tissues and organs from blood circulation, as well as the underlying implications of potential harmful health effects in human.</p> <p>Results</p> <p>The confocal microscopy imaging analysis demonstrates that exposure to engineered iron nanoparticles induces an increase in cell permeability in human microvascular endothelial cells. Our studies further reveal iron nanoparticles enhance the permeability through the production of reactive oxygen species (ROS) and the stabilization of microtubules. We also showed Akt/GSK-3β signaling pathways are involved in iron nanoparticle-induced cell permeability. The inhibition of ROS demonstrate ROS play a major role in regulating Akt/GSK-3β – mediated cell permeability upon iron nanoparticle exposure. These results provide new insights into the bioreactivity of engineered iron nanoparticles which can inform potential applications in medical imaging or drug delivery.</p> <p>Conclusion</p> <p>Our results indicate that exposure to iron nanoparticles induces an increase in endothelial cell permeability through ROS oxidative stress-modulated microtubule remodeling. The findings from this study provide new understandings on the effects of nanoparticles on vascular transport of macromolecules and drugs.</p> |
url |
http://www.particleandfibretoxicology.com/content/6/1/1 |
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