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Adsorption of Surfactant Lipids by Single-Walled Carbon Nanotubes in Mouse Lung upon Pharyngeal Aspiration: Role in Uptake by Macrophages

机译:小鼠肺部单壁碳纳米管吸附表面活性剂脂质在咽部咽部作用下的作用:巨噬细胞吸收的作用

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摘要

The pulmonary route represents one of the most important portals of entry for nanoparticles into the body. However, the in vivo interactions of nanoparticles with biomolecules of the lung have not been sufficiently studied. Here, using an established mouse model of pharyngeal aspiration of single-walled carbon nanotubes (SWCNTs), we recovered SWCNTs from the bronchoalveolar lavage fluid (BALf), purified them from possible contamination with lung cells and examined the composition of phospholipids adsorbed on SWCNTs by liquid chromatography mass spectrometry (LC-MS) analysis. We found that SWCNTs selectively adsorbed two types of the most abundant surfactant phospholipids – phosphatidylcholines (PC) and phosphatidylglycerols (PG). Molecular speciation of these phospholipids was also consistent with pulmonary surfactant. Quantitation of adsorbed lipids by LC-MS along with the structural assessments of phospholipid binding by atomic force microscopy and molecular modeling indicated that the phospholipids (~108 molecules per SWCNT) formed an uninterrupted “coating” whereby the hydrophobic alkyl chains of the phospholipids were adsorbed onto the SWCNT with the polar head groups pointed away from the SWCNT into the aqueous phase. In addition, the presence of surfactant proteins A, B and D on SWCNTs was determined by LC-MS. Finally, we demonstrated that the presence of this surfactant coating markedly enhanced the in vitro uptake of SWCNTs by macrophages. Taken together, this is the first demonstration of the in vivo adsorption of the surfactant lipids and proteins on SWCNTs in a physiologically relevant animal model.
机译:肺路线代表纳米颗粒进入体内最重要的门站之一。然而,纳米颗粒与肺部生物分子的体内相互作用未得到充分研究。这里,使用单壁碳纳米管(SWCNTs)的咽部咽部吸入的已建立的小鼠模型,从支气管肺泡灌洗液(BALF)中回收SWCNT,从肺细胞中纯化它们,并检查吸附在SWCNT上的磷脂的组成液相色谱质谱(LC-MS)分析。我们发现SWCNTS选择性地吸附了两种类型的最丰富的表面活性剂磷脂 - 磷脂酰胆碱(PC)和磷脂酰甘油(PG)。这些磷脂的分子形状也与肺表面活性剂一致。通过LC-MS定量吸附的脂质以及通过原子力显微镜和分子建模的磷脂结合的结构评估表明,磷脂(每SWCNT的〜108分子)形成不间断的“涂层”,从而吸附了磷脂的疏水烷基链的疏水烷基链与SWCNT到远离SWCNT的极性头部进入水相。另外,通过LC-MS测定SWCNT上的表面活性剂蛋白A,B和D的存在。最后,我们证明了这种表面活性剂涂层的存在明显增强了巨噬细胞的SWCNT的体外吸收。连同,这是生理相关的动物模型中的表面活性剂脂质和蛋白质的体内吸附的第一次证明。

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