Binding of pulmonary surfactant proteins to carbon nanotubes;: potential for damage to lung immune defense mechanisms

被引:79
|
作者
Salvador-Morales, Carolina
Townsend, Paul
Flahaut, Emmanuel
Venien-Bryan, Catherine
Vlandas, Alexis
Green, Malcolm L. H.
Sim, Robert B.
机构
[1] Univ Oxford, Dept Biochem, MRC Immunochem Unit, Oxford OX1 3QU, England
[2] Univ Oxford, Inorgan Chem Lab, Oxford OX1 3QR, England
[3] Univ Toulouse 3, Ctr Interuniv Rech & Ingn Mat, F-31062 Toulouse, France
[4] Univ Oxford, Dept Biochem, Mol Biophys Lab, Oxford OX1 3QU, England
[5] Univ Oxford, Dept Mat, Oxford OX1 3PH, England
基金
英国医学研究理事会;
关键词
D O I
10.1016/j.carbon.2006.10.011
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Potential pulmonary toxicity of carbon nanotubes is a research area that has received considerable attention. Surfactant proteins A and D (SP-A and SP-D) are collectin proteins that are secreted by airway epithelial cells in the lung. They play an important role in first-line defense against infection within the lung. The aim of this study was to investigate the interaction between carbon nanotubes and proteins contained in lung surfactant. By using sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SIDS-PAGE), Western Blotting, a novel technique of affinity chromatography based on carbon nanotube-Sepharose matrix [1] and electron microscopy data it was shown that SP-A and SP-D selectively bind to carbon nanotubes. The binding was Ca2+-ion dependent, and was variable between batches of nanotubes. It was therefore likely to be mediated by surface impurities or chemical modifications of the nanotubes. Chronic level exposure to carbon nanotubes may result in sequestration of SP-D and SP-A. Absence of these proteins in knockout mice leads to susceptibility to lung infection and emphysema. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:607 / 617
页数:11
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