School of Biomedical Engineering, School of Chemistry and Chemical Engineering, National Center for Translational Medicine, Shanghai Jiao Tong University, 200240 Shanghai, China.
ACS Biomater Sci Eng. 2024 Sep 9;10(9):5609-5616. doi: 10.1021/acsbiomaterials.4c00546. Epub 2024 May 22.
Visualizing the whole vascular network system is crucial for understanding the pathogenesis of specific diseases and devising targeted therapeutic interventions. Although the combination of light sheet microscopy and tissue-clearing methods has emerged as a promising approach for investigating the blood vascular network, leveraging the spatial resolution down to the capillary level and the ability to image centimeter-scale samples remains difficult. Especially, as the resolution improves, the issue of photobleaching outside the field of view poses a challenge to image the whole vascular network of adult mice at capillary resolution. Here, we devise a fluorescent microsphere vascular perfusion method to enable labeling of the whole vascular network in adult mice, which overcomes the photobleaching limit during the imaging of large samples. Moreover, by combining the utilization of a large-scale light-sheet microscope and tissue clearing protocols for whole-mouse samples, we achieve the capillary-level imaging resolution (3.2 × 3.2 × 6.5 μm) of the whole vascular network with dimensions of 45 × 15 × 82 mm in adult mice. This method thus holds great potential to deliver mesoscopic resolution images of various tissue organs for whole-animal imaging.
可视化整个血管网络系统对于理解特定疾病的发病机制和设计靶向治疗干预措施至关重要。尽管光片显微镜和组织透明化方法的结合已成为研究血液血管网络的一种有前途的方法,但要实现亚毫米级分辨率和对厘米级样本进行成像仍然具有挑战性。特别是,随着分辨率的提高,视野外的光漂白问题对以毛细血管分辨率对成年小鼠的整个血管网络进行成像构成了挑战。在这里,我们设计了一种荧光微球血管灌注方法,使成年小鼠的整个血管网络能够被标记,从而克服了在大样本成像过程中的光漂白限制。此外,通过结合利用大规模光片显微镜和用于全鼠样本的组织透明化方案,我们实现了整个血管网络的毛细血管水平成像分辨率(3.2×3.2×6.5μm),并对成年小鼠的 45×15×82mm 尺寸的血管网络进行成像。因此,该方法有望为全动物成像提供各种组织器官的介观分辨率图像。