显微镜
双光子激发显微术
病理
临床前影像学
荧光显微镜
活体显微镜检查
体内
共焦显微镜
荧光寿命成像显微镜
淀粉样蛋白(真菌学)
海马体
生物物理学
化学
荧光
生物
光学
医学
神经科学
细胞生物学
物理
生物技术
作者
Ruiqing Ni,Zhenyue Chen,Xosé Luís Deán‐Ben,Fabian F. Voigt,Daniel S. Kirschenbaum,Gloria Shi,Alessia Villois,Quanyu Zhou,Alessandro Crimi,Paolo Arosio,Roger M. Nitsch,K. Peter R. Nilsson,Adriano Aguzzi,Fritjof Helmchen,Jan Klohs,Daniel Razansky
标识
DOI:10.1038/s41551-022-00906-1
摘要
Deposits of amyloid-β (Aβ) in the brains of rodents can be analysed by invasive intravital microscopy on a submillimetre scale, or via whole-brain images from modalities lacking the resolution or molecular specificity to accurately characterize Aβ pathologies. Here we show that large-field multifocal illumination fluorescence microscopy and panoramic volumetric multispectral optoacoustic tomography can be combined to longitudinally assess Aβ deposits in transgenic mouse models of Alzheimer's disease. We used fluorescent Aβ-targeted probes (the luminescent conjugated oligothiophene HS-169 and the oxazine-derivative AOI987) to transcranially detect Aβ deposits in the cortex of APP/PS1 and arcAβ mice with single-plaque resolution (8 μm) and across the whole brain (including the hippocampus and the thalamus, which are inaccessible by conventional intravital microscopy) at sub-150 μm resolutions. Two-photon microscopy, light-sheet microscopy and immunohistochemistry of brain-tissue sections confirmed the specificity and regional distributions of the deposits. High-resolution multiscale optical and optoacoustic imaging of Aβ deposits across the entire brain in rodents thus facilitates the in vivo study of Aβ accumulation by brain region and by animal age and strain.
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