| Literature DB >> 30135307 |
Yichen Ding1,2, Jianguo Ma1,3,4, Adam D Langenbacher5, Kyung In Baek2, Juhyun Lee2, Chih-Chiang Chang2, Jeffrey J Hsu1, Rajan P Kulkarni1, John Belperio1, Wei Shi6, Sara Ranjbarvaziri1, Reza Ardehali1, Yin Tintut1, Linda L Demer1, Jau-Nian Chen5, Peng Fei1,7, René R Sevag Packard1, Tzung K Hsiai1,2.
Abstract
The ability to image tissue morphogenesis in real-time and in 3-dimensions (3-D) remains an optical challenge. The advent of light-sheet fluorescence microscopy (LSFM) has advanced developmental biology and tissue regeneration research. In this review, we introduce a LSFM system in which the illumination lens reshapes a thin light-sheet to rapidly scan across a sample of interest while the detection lens orthogonally collects the imaging data. This multiscale strategy provides deep-tissue penetration, high-spatiotemporal resolution, and minimal photobleaching and phototoxicity, allowing in vivo visualization of a variety of tissues and processes, ranging from developing hearts in live zebrafish embryos to ex vivo interrogation of the microarchitecture of optically cleared neonatal hearts. Here, we highlight multiple applications of LSFM and discuss several studies that have allowed better characterization of developmental and pathological processes in multiple models and tissues. These findings demonstrate the capacity of multiscale light-sheet imaging to uncover cardiovascular developmental and regenerative phenomena.Entities:
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Year: 2018 PMID: 30135307 PMCID: PMC6141183 DOI: 10.1172/jci.insight.121396
Source DB: PubMed Journal: JCI Insight ISSN: 2379-3708