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Multiwalled Carbon Nanotubes Hinder Microglia Function Interfering with Cell Migration and Phagocytosis

The intranasal drug delivery route provides exciting expectations regarding the application of engineered nanomaterials as nano‐medicines or drug‐delivery vectors into the brain. Among nanomaterials, multiwalled CNTs (MWCNTs) are some of the best candidates for brain cancer therapy since they are we...

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Bibliographic Details
Published in:Advanced healthcare materials 2014-03, Vol.3 (3), p.424-432
Main Authors: Villegas, Juan C., Álvarez-Montes, Laura, Rodríguez-Fernández, Lidia, González, Jesús, Valiente, Rafael, Fanarraga, Mónica L.
Format: Article
Language:English
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Summary:The intranasal drug delivery route provides exciting expectations regarding the application of engineered nanomaterials as nano‐medicines or drug‐delivery vectors into the brain. Among nanomaterials, multiwalled CNTs (MWCNTs) are some of the best candidates for brain cancer therapy since they are well known to go across cellular barriers and display an intrinsic ability to block cancer cell proliferation triggering apoptosis. This study reveals that microglial cells, the brain macrophages and putative vehicles for MWCNTs into the brain, undergo a dose‐dependent cell division arrest and apoptosis when treated with MWCNTs. Moreover, it is shown that MWCNTs severely interfere with both cell migration and phagocytosis in live microglia. These results lead to a re‐evaluation of the safety of inhaled airborne CNTs and provide strategic clues of how to biocompatibilize MWCNTs to reduce brain macrophage damage and to develop new nanodrugs. Microglial cells undergo a dose‐dependent cell division arrest and apoptosis when treated with multiwalled carbon nanotubes (MWCNTs). It is shown that how MWCNTs severely interfere with both cell migration and phagocytosis in live microglia. These results provide strategic clues of how to biocompatibilize MWCNTs to reduce the damage in brain macrophages to develop new nanodrugs based on MWCNTs.
ISSN:2192-2640
2192-2659
DOI:10.1002/adhm.201300178