| Literature DB >> 30775081 |
Haoyu Li1,2, Changliang Guo3, Deborah Kim-Holzapfel4, Weiyi Li5, Yelena Altshuller6, Bryce Schroeder1,7, Wenhao Liu3, Yizhi Meng5, Jarrod B French4, Ken-Ichi Takamaru6, Michael A Frohman6,7, Shu Jia3.
Abstract
Visualizing diverse anatomical and functional traits that span many spatial scales with high spatio-temporal resolution provides insights into the fundamentals of living organisms. Light-field microscopy (LFM) has recently emerged as a scanning-free, scalable method that allows for high-speed, volumetric functional brain imaging. Given those promising applications at the tissue level, at its other extreme, this highly-scalable approach holds great potential for observing structures and dynamics in single-cell specimens. However, the challenge remains for current LFM to achieve a subcellular level, near-diffraction-limited 3D spatial resolution. Here, we report high-resolution LFM (HR-LFM) for live-cell imaging with a resolution of 300-700 nm in all three dimensions, an imaging depth of several micrometers, and a volume acquisition time of milliseconds. We demonstrate the technique by imaging various cellular dynamics and structures and tracking single particles. The method may advance LFM as a particularly useful tool for understanding biological systems at multiple spatio-temporal levels.Entities:
Year: 2018 PMID: 30775081 PMCID: PMC6363205 DOI: 10.1364/BOE.10.000029
Source DB: PubMed Journal: Biomed Opt Express ISSN: 2156-7085 Impact factor: 3.732