首页> 美国卫生研究院文献>Journal of Visualized Experiments : JoVE >A Novel High-resolution In vivo Imaging Technique to Study the Dynamic Response of Intracranial Structures to Tumor Growth and Therapeutics
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A Novel High-resolution In vivo Imaging Technique to Study the Dynamic Response of Intracranial Structures to Tumor Growth and Therapeutics

机译:一种新颖的高分辨率体内成像技术以研究颅内结构对肿瘤生长和治疗的动态响应。

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摘要

We have successfully integrated previously established Intracranial window (ICW) technology 1-4 with intravital 2-photon confocal microscopy to develop a novel platform that allows for direct long-term visualization of tissue structure changes intracranially. Imaging at a single cell resolution in a real-time fashion provides supplementary dynamic information beyond that provided by standard end-point histological analysis, which looks solely at 'snap-shot' cross sections of tissue.Establishing this intravital imaging technique in fluorescent chimeric mice, we are able to image four fluorescent channels simultaneously. By incorporating fluorescently labeled cells, such as GFP+ bone marrow, it is possible to track the fate of these cells studying their long-term migration, integration and differentiation within tissue. Further integration of a secondary reporter cell, such as an mCherry glioma tumor line, allows for characterization of cell:cell interactions. Structural changes in the tissue microenvironment can be highlighted through the addition of intra-vital dyes and antibodies, for example CD31 tagged antibodies and Dextran molecules.Moreover, we describe the combination of our ICW imaging model with a small animal micro-irradiator that provides stereotactic irradiation, creating a platform through which the dynamic tissue changes that occur following the administration of ionizing irradiation can be assessed.Current limitations of our model include penetrance of the microscope, which is limited to a depth of up to 900 μm from the sub cortical surface, limiting imaging to the dorsal axis of the brain. The presence of the skull bone makes the ICW a more challenging technical procedure, compared to the more established and utilized chamber models currently used to study mammary tissue and fat pads 5-7. In addition, the ICW provides many challenges when optimizing the imaging.
机译:我们已经成功地将先前建立的颅内窗(ICW)技术 1-4 与活体2光子共聚焦显微镜相结合,以开发出一个新颖的平台,可以直接长期可视地显示颅内的组织结构变化。在单细胞分辨率下以实时方式成像可提供除标准终点组织学分析所提供的动态信息之外的补充动态信息,标准组织学分析仅查看组织的``快照''横截面。在荧光嵌合体小鼠中建立这种活体成像技术,我们能够同时成像四个荧光通道。通过掺入荧光标记的细胞(例如GFP +骨髓),有可能追踪这些细胞的命运,研究它们在组织内的长期迁移,整合和分化。继发报告细胞(例如mCherry胶质瘤肿瘤细胞系)的进一步整合可表征细胞:细胞相互作用。通过添加活体内染料和抗体(例如CD31标记的抗体和葡聚糖分子)可以突出显示组织微环境的结构变化。此外,我们描述了ICW成像模型与提供立体定位的小型动物微辐照器的结合辐照,建立了一个平台,通过该平台可以评估电离辐照后发生的动态组织变化。我们模型的当前局限性包括显微镜的渗透率,该渗透率仅限于距皮层下表面最多900μm的深度,将影像限制在大脑的背轴上。与目前用于研究乳腺组织和脂肪垫 5-7 的更成熟和使用的腔室模型相比,颅骨的存在使ICW更具挑战性。另外,在优化成像时,ICW带来了许多挑战。

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