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3D Imaging and Quantitative Analysis of Vascular Networks: A Comparison of Ultramicroscopy and Micro-Computed Tomography

机译:血管网络的3D成像和定量分析:超显微技术和计算机断层扫描技术的比较

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摘要

Rationale: Classic histology is the gold standard for vascular network imaging and analysis. The method however is laborious and prone to artefacts. Here, the suitability of ultramicroscopy (UM) and micro-computed tomography (CT) was studied to establish potential alternatives to histology.Methods: The vasculature of murine organs (kidney, heart and atherosclerotic carotid arteries) was visualized using conventional 2D microscopy, 3D light sheet ultramicroscopy (UM) and micro-CT. Moreover, spheroid-based human endothelial cell vessel formation in mice was quantified. Fluorescently labeled Isolectin GS-IB4 A647 was used for in vivo labeling of vasculature for UM analysis, and analyses were performed ex vivo after sample preparation. For CT imaging, animals were perfused postmortem with radiopaque contrast agent.Results: Using UM imaging, 3D vascular network information could be obtained in samples of animals receiving in vivo injection of the fluorescently labeled Isolectin GS-IB4. Resolution was sufficient to measure single endothelial cell integration into capillaries in the spheroid-based matrigel plug assay. Because of the selective staining of the endothelium, imaging of larger vessels yielded less favorable results. Using micro-CT or even nano-CT, imaging of capillaries was impossible due to insufficient X-ray absorption and thus insufficient signal-to-noise ratio. Identification of lumen in murine arteries using micro-CT was in contrast superior to UM.Conclusion: UM and micro-CT are two complementary techniques. Whereas UM is ideal for imaging and especially quantifying capillary networks and arterioles, larger vascular structures are easier and faster to quantify and visualize using micro-CT. 3D information of both techniques is superior to 2D histology. UM and micro-CT together may open a new field of clinical pathology diagnosis.
机译:基本原理:经典组织学是血管网络成像和分析的黄金标准。然而,该方法费力并且容易产生伪像。在此,研究了超显微技术(UM)和计算机断层摄影技术(CT)的适用性,以建立可能的组织学替代方法。光学薄板超显微镜(UM)和微型CT。此外,对小鼠中基于球体的人内皮细胞血管形成进行了定量。荧光标记的Isolectin GS-IB4 A647用于体内标记脉管系统以进行UM分析,并在样品制备后进行离体分析。结果:使用UM成像,可以在体内注射荧光标记的Isolectin GS-IB4的动物样品中获得3D血管网络信息。分辨率足以在基于球体的基质胶塞测定中测量单个内皮细胞整合入毛细血管中。由于内皮的选择性染色,较大血管的成像产生较差的结果。使用微CT或什至是纳米CT,由于X射线吸收不足,因此信噪比不足,无法对毛细管进行成像。相比之下,使用微CT鉴定鼠动脉内腔的能力优于UM。结论:UM和微CT是两种互补的技术。 UM是成像尤其是定量毛细管网络和小动脉的理想选择,而较大的血管结构更易于使用micro-CT定量和可视化。两种技术的3D信息均优于2D组织学。 UM和micro-CT一起可以开辟临床病理诊断的新领域。

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