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Scavenger receptor mediated endocytosis of silver nanoparticles into J774A.1 macrophages is heterogeneous

机译:清道夫受体介导的银纳米颗粒向J774A.1巨噬细胞的内吞作用是异质的

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摘要

We investigated the scavenger receptor mediated uptake and subsequent intracellular spatial distribution and clustering of 57.7 ± 6.9 nm diameter silver nanoparticles (zeta-potential = -28.4 mV) in the murine macrophage cell line J774A.1 through colorimetric imaging. The NPs exhibited an overall red-shift of the plasmon resonance wavelength in the cell ensemble as function of time and concentration, indicative of intracellular NP agglomeration. A detailed analysis of the NP clustering in individual cells revealed a strong phenotypic variability in the intracellular NP organization on the single cell level. Throughout the observation time of 24h cells containing non- or low-agglomerated NPs with a characteristic blue color coexisted with cells containing NPs with varying degrees of agglomeration, as evinced by distinct spectral shifts of their resonance wavelengths. Pharmacological inhibition studies indicated that the observed differences in intracellular NP organization resulted from coexisting actin- and clathrin-dependent endocytosis mechanisms in the macrophage population. Correlation of intracellular NP clustering with macrophage maturity marker (F4/80, CD14) expression revealed that differentiated J774A.1 cells preferentially contained compact NP agglomerates, whereas monocyte-like macrophages contained non-agglomerated NPs.
机译:我们通过比色成像研究了鼠巨噬细胞系J774A.1中清道夫受体介导的摄取以及随后的细胞内空间分布和簇状的57.7±6.9 nm直径的银纳米颗粒(ζ电势= -28.4 mV)。 NP在细胞集合中表现出等离振子共振波长的整体红移,其是时间和浓度的函数,表明细胞内NP聚集。对单个细胞中NP簇的详细分析显示,在单个细胞水平上,细胞内NP组织中存在很强的表型变异性。在整个24小时的观察时间内,包含具有特征性蓝色的非聚集或低聚集NP的细胞与包含具有不同聚集度的NP的细胞共存,这由其共振波长的明显光谱偏移所证实。药理抑制研究表明,观察到的细胞内NP组织差异是由于巨噬细胞群体中肌动蛋白和网格蛋白依赖性内吞机制共存所致。细胞内NP聚类与巨噬细胞成熟标记(F4 / 80,CD14)表达的相关性表明,分化的J774A.1细胞优先含有紧密的NP团聚体,而单核细胞样巨噬细胞则含有非聚集的NP。

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