多细胞生物
细胞器
显微镜
生物系统
活体细胞成像
分辨率(逻辑)
时间分辨率
生物物理学
生物
光学
细胞
物理
计算机科学
细胞生物学
人工智能
遗传学
作者
Tsung‐Li Liu,Srigokul Upadhyayula,Daniel E. Milkie,Ved Singh,Kai Wang,Ian A. Swinburne,Kishore Mosaliganti,Zach M. Collins,Tom W. Hiscock,Jamien Shea,Abraham Q. Kohrman,Taylor N. Medwig-Kinney,Daphné Dambournet,Ryan Forster,Brian Cunniff,Yuan Ruan,Hanako Yashiro,Steffen Scholpp,Elliot M. Meyerowitz,Dirk Hockemeyer
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2018-04-20
卷期号:360 (6386)
被引量:540
标识
DOI:10.1126/science.aaq1392
摘要
Continuing the resolution revolution The living cell contains dynamic, spatially complex subassemblies that are sensitive to external perturbations. To minimize such perturbations, cells should be imaged in their native multicellular environments, under as gentle illumination as possible. However, achieving the spatiotemporal resolution needed to follow three-dimensional subcellular processes in detail under these conditions is challenging: Sample-induced aberrations degrade resolution and sensitivity, and high resolution usually requires intense excitation. Liu et al. combined noninvasive lattice light-sheet microscopy with aberration-correcting adaptive optics to study a variety of delicate subcellular events in vivo, including organelle remodeling during mitosis and growth cone dynamics during spinal cord development. Science , this issue p. eaaq1392
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