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ToxSci Advance Access originally published online on March 14, 2007
Toxicological Sciences 2007 97(2):398-406; doi:10.1093/toxsci/kfm050
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© The Author 2007. Published by Oxford University Press on behalf of the Society of Toxicology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

A Murine Scavenger Receptor MARCO Recognizes Polystyrene Nanoparticles

Sanae Kanno1, Akiko Furuyama and Seishiro Hirano

Environmental Nanotoxicology Section, Research Center for Environmental Risk, National Institute for Environmental Studies, 16-2 Onogawa, Tsukuba, Ibaraki 305-8506, Japan

1 To whom correspondence should be addressed. Fax: +81-29-850-2512. E-mail: sanae{at}nies.go.jp.

Received December 28, 2006; accepted February 27, 2007


   Abstract

Recent toxicological studies indicate that nanoparticles or ultrafine particles (< 100 nm) are more toxic than fine particles (< 2 µm) because of their greater surface area. It is well known that alveolar macrophages play an important role in the first defense against various environmental particles and microorganisms. This is accomplished by binding to a macrophage receptor with collagenous structure (MARCO), one of several scavenger-type receptors expressed on the cell surface of macrophages. MARCO has been shown to mediate the ingestion of unopsonized environmental particles such as TiO2 and Fe2O3 (1.3 µm in diameter). However, very little is known about the cellular uptake of nanoparticles. In the present study, we investigated whether MARCO mediates the uptake of nanoparticles by using fluorescent-tagged polystyrene particles (20 nm, 200 nm, and 1 µm in diameter). COS-7 cells were transfected with either MARCO cDNA or an empty vector, and the association of the particles with the cells were observed by fluorescence microscopy and atomic force microscopy. MARCO-transfected cells associated with all three sizes of particles in a time-dependent manner, while no obvious binding of particles occurred after 5 h to the empty vector–transfected cells. The uptake of particles by MARCO-transfected cells was partially inhibited by polyG. These results suggest that macrophages associate with nanoparticles (20 nm) at least in part through MARCO and that MARCO plays a role in clearing nanoparticles which can deposit in the alveolar region.

Key Words: MARCO; nanoparticles; COS-7; atomic force microscopy; fluorescence microscopy.


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[Abstract] [Full Text] [PDF]



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