| Literature DB >> 33398061 |
Chunyu Fang1, Tingting Yu2,3, Tingting Chu1, Wenyang Feng1, Fang Zhao1, Xuechun Wang1, Yujie Huang4, Yusha Li2, Peng Wan2, Wei Mei5, Dan Zhu6,7, Peng Fei8.
Abstract
Rapid 3D imaging of entire organs and organisms at cellular resolution is a recurring challenge in life science. Here we report on a computational light-sheet microscopy able to achieve minute-timescale high-resolution mapping of entire macro-scale organs. Through combining a dual-side confocally-scanned Bessel light-sheet illumination which provides thinner-and-wider optical sectioning of deep tissues, with a content-aware compressed sensing (CACS) computation pipeline which further improves the contrast and resolution based on a single acquisition, our approach yields 3D images with high, isotropic spatial resolution and rapid acquisition over two-order-of-magnitude faster than conventional 3D microscopy implementations. We demonstrate the imaging of whole brain (~400 mm3), entire gastrocnemius and tibialis muscles (~200 mm3) of mouse at ultra-high throughput of 5~10 min per sample and post-improved subcellular resolution of ~ 1.5 μm (0.5-μm iso-voxel size). Various system-level cellular analyses, such as mapping cell populations at different brain sub-regions, tracing long-distance projection neurons over the entire brain, and calculating neuromuscular junction occupancy across whole muscle, are also readily accomplished by our method.Entities:
Year: 2021 PMID: 33398061 DOI: 10.1038/s41467-020-20329-3
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919