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Three-dimensional ultrastructural imaging reveals the nanoscale architecture of mammalian cells

机译:三维超微结构成像揭示了哺乳动物细胞的纳米结构

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摘要

Knowledge of the interactions between nanomaterials and large-size mammalian cells, including cellular uptake, intracellular localization and translocation, has greatly advanced nanomedicine and nanotoxicology. Imaging techniques that can locate nanomaterials within the structures of intact large-size cells at nanoscale resolution play crucial roles in acquiring this knowledge. Here, the quantitative imaging of intracellular nanomaterials in three dimensions was performed by combining dual-energy contrast X-ray microscopy and an iterative tomographic algorithm termed equally sloped tomography (EST). Macrophages with a size of ∼20 µm that had been exposed to the potential antitumour agent [Gd@C82(OH)22]n were investigated. Large numbers of nanoparticles (NPs) aggregated within the cell and were mainly located in phagosomes. No NPs were observed in the nucleus. Imaging of the nanomedicine within whole cells advanced the understanding of the high-efficiency antitumour activity and the low toxicity of this agent. This imaging technique can be used to probe nanomaterials within intact large-size cells at nanometre resolution uniformly in three dimensions and may greatly benefit the fields of nanomedicine and nanotoxicology.
机译:纳米材料与大型哺乳动物细胞之间相互作用的知识,包括细胞摄取,细胞内定位和易位,已经大大提高了纳米医学和纳米毒理学的水平。可以将纳米材料定位在完整的大尺寸细胞结构中且具有纳米级分辨率的成像技术,在获取此知识方面起着至关重要的作用。在这里,通过结合双能量对比X射线显微镜技术和称为等效倾斜层析成像(EST)的迭代层析成像算法对三维内细胞内纳米材料进行定量成像。研究了已经暴露于潜在抗肿瘤药[Gd @ C82(OH)22] n的大小约为20μm的巨噬细胞。大量的纳米粒子(NPs)聚集在细胞内,主要位于吞噬体中。在细胞核中未观察到NP。全细胞内纳米药物的成像促进了对该药物高效抗肿瘤活性和低毒性的认识。该成像技术可用于在三个维度上以纳米分辨率均匀地探测完整大细胞内的纳米材料,并且可能极大地有益于纳米医学和纳米毒理学领域。

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