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Colloidal Gold Nanoparticles Induce Changes in Cellular and Subcellular Morphology

机译:胶体金纳米颗粒诱导细胞和亚细胞形态的变化

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摘要

Exposure of cells to colloidal nanoparticles (NPs) can have concentration-dependent harmful effects. Mostly, such effects are monitored with biochemical assays or probes from molecular biology, i.e., viability assays, gene expression profiles, etc., neglecting that the presence of NPs can also drastically affect cellular morphology. In the case of polymer-coated Au NPs, we demonstrate that upon NP internalization, cells undergo lysosomal swelling, alterations in mitochondrial morphology, disturbances in actin and tubulin cytoskeleton and associated signaling, and reduction of focal adhesion contact area and number of filopodia. Appropriate imaging and data treatment techniques allow for quantitative analyses of these concentration-dependent changes. Abnormalities in morphology occur at similar (or even lower) NP concentrations as the onset of reduced cellular viability. Cellular morphology is thus an important quantitative indicator to verify harmful effects of NPs to cells, without requiring biochemical assays, but relying on appropriate staining and imaging techniques.
机译:细胞暴露于胶体纳米颗粒(NPS)可以具有浓度依赖性的有害作用。大多数情况下,通过来自分子生物学的生物化学测定或探针监测这种效果,即生存能测定,基因表达谱等,忽略了NPS的存在也可以显着影响细胞形态。在聚合物涂覆的Au NPS的情况下,我们证明,在NP内化时,细胞经历溶酶体肿胀,线粒体形态的改变,肌动蛋白和小管蛋白细胞骨骼的干扰以及相关的信号传导,以及减少局灶性粘附接触面积和箔的数量。适当的成像和数据处理技术允许这些浓度依赖性变化的定量分析。形态学的异常发生在类似(或甚至较低)NP浓度下,作为细胞活力降低的发作。因此,细胞形态是一种重要的定量指标,用于验证NPS对细胞的有害影响,而不需要生化测定,但依赖于适当的染色和成像技术。

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