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Fast, volumetric live-cell imaging using high-resolution light-field microscopy

  • Haoyu Li
  • , Changliang Guo
  • , Deborah Kim-Holzapfel
  • , Weiyi Li
  • , Yelena Altshuller
  • , Bryce Schroeder
  • , Wenhao Liu
  • , Yizhi Meng
  • , Jarrod B. French
  • , Ken Ichi Takamaru
  • , Michael A. Frohman
  • , Shu Jia
  • Stony Brook University
  • Harbin Institute of Technology
  • Emory University

Research output: Contribution to journalArticlepeer-review

112 Scopus citations

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.

Original languageEnglish
Pages (from-to)29-49
Number of pages21
JournalBiomedical Optics Express
Volume10
Issue number1
DOIs
StatePublished - 2019

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