Skip to main navigation Skip to search Skip to main content

Imaging multicellular specimens with real-time optimized tiling light-sheet selective plane illumination microscopy

  • Stony Brook University

Research output: Contribution to journalArticlepeer-review

91 Scopus citations

Abstract

Despite the progress made in selective plane illumination microscopy, high-resolution 3D live imaging of multicellular specimens remains challenging. Tiling light-sheet selective plane illumination microscopy (TLS-SPIM) with real-time light-sheet optimization was developed to respond to the challenge. It improves the 3D imaging ability of SPIM in resolving complex structures and optimizes SPIM live imaging performance by using a real-time adjustable tiling light sheet and creating a flexible compromise between spatial and temporal resolution. We demonstrate the 3D live imaging ability of TLS-SPIM by imaging cellular and subcellular behaviours in live C. elegans and zebrafish embryos, and show how TLS-SPIM can facilitate cell biology research in multicellular specimens by studying left-right symmetry breaking behaviour of C. elegans embryos.

Original languageEnglish
Article number11088
JournalNature Communications
Volume7
DOIs
StatePublished - Mar 23 2016

Fingerprint

Dive into the research topics of 'Imaging multicellular specimens with real-time optimized tiling light-sheet selective plane illumination microscopy'. Together they form a unique fingerprint.

Cite this