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Correlative imaging of single carbon nanotubes and fluorescently labelled neuronal structures in the extracellular space of live brains

机译:活脑细胞外空间中单个碳纳米管和荧光标记的神经元结构的相关成像

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The brain extracellular space (ECS) is a complex network that constitutes a key microenvironment for cellular communication, homeostasis, and clearance of toxic metabolites. Signaling molecules, neuromodulators, and nutrients transit via the ECS, therefore mediating the communication between cells. Despite the relevance of this important part of the brain, its dynamics and structural organization at the nanoscale is still mostly unknown. We have recently demonstrated that single-walled carbon nanotubes (SWCNTs) can be used to image and probe live brain tissue, providing super-resolved maps of the brain ECS and quantitative information on the local diffusion environment. Here, we propose an important refinement of this approach by implementing a structured illumination technique (named HiLo microscopy) to image fluorescently labelled neuronal structures in parallel to SWCNT NIR imaging. This technique is based on speckle illumination and relies on the acquisition of one structured and one uniform illumination image to obtain images deep into tissues with good optical sectioning. Having access to spatially resolved SWCNT diffusivity around specific neuronal structures will provide more precise insights about the heterogeneity of the brain environment.
机译:脑细胞外空间(ECS)是一个复杂的网络,构成了细胞通讯,体内平衡和清除有毒代谢产物的关键微环境。信号分子,神经调节剂和营养物质通过ECS转运,因此介导细胞之间的通讯。尽管大脑的这一重要部分具有相关性,但在纳米尺度上其动力学和结构组织仍是未知之数。最近,我们证明了单壁碳纳米管(SWCNT)可用于成像和探测活的大脑组织,提供大脑ECS的超分辨图和局部扩散环境的定量信息。在这里,我们通过实现结构化的照明技术(称为HiLo显微镜)对荧光标记的神经元结构进行成像,与SWCNT NIR成像并行进行,提出了对该方法的重要改进。该技术基于散斑照明,并依赖于获取一个结构化和一个均匀的照明图像,以获得具有良好光学切片的深入组织的图像。可以访问特定神经元结构周围空间分辨的SWCNT扩散系数,这将提供有关大脑环境异质性的更精确的见解。

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