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High-contrast, synchronous volumetric imaging with selective volume illumination microscopy.
Truong, Thai V; Holland, Daniel B; Madaan, Sara; Andreev, Andrey; Keomanee-Dizon, Kevin; Troll, Josh V; Koo, Daniel E S; McFall-Ngai, Margaret J; Fraser, Scott E.
Afiliação
  • Truong TV; Translational Imaging Center, University of Southern California, Los Angeles, CA, 90089, USA. tvtruong@usc.edu.
  • Holland DB; Molecular and Computational Biology Section, University of Southern California, Los Angeles, CA, 90089, USA. tvtruong@usc.edu.
  • Madaan S; Translational Imaging Center, University of Southern California, Los Angeles, CA, 90089, USA.
  • Andreev A; Translational Imaging Center, University of Southern California, Los Angeles, CA, 90089, USA.
  • Keomanee-Dizon K; Department of Biomedical Engineering, University of Southern California, Los Angeles, CA, 90089, USA.
  • Troll JV; Translational Imaging Center, University of Southern California, Los Angeles, CA, 90089, USA.
  • Koo DES; Department of Biomedical Engineering, University of Southern California, Los Angeles, CA, 90089, USA.
  • McFall-Ngai MJ; Translational Imaging Center, University of Southern California, Los Angeles, CA, 90089, USA.
  • Fraser SE; Translational Imaging Center, University of Southern California, Los Angeles, CA, 90089, USA.
Commun Biol ; 3(1): 74, 2020 02 14.
Article em En | MEDLINE | ID: mdl-32060411
ABSTRACT
Light-field fluorescence microscopy uniquely provides fast, synchronous volumetric imaging by capturing an extended volume in one snapshot, but often suffers from low contrast due to the background signal generated by its wide-field illumination strategy. We implemented light-field-based selective volume illumination microscopy (SVIM), where illumination is confined to only the volume of interest, removing the background generated from the extraneous sample volume, and dramatically enhancing the image contrast. We demonstrate the capabilities of SVIM by capturing cellular-resolution 3D movies of flowing bacteria in seawater as they colonize their squid symbiotic partner, as well as of the beating heart and brain-wide neural activity in larval zebrafish. These applications demonstrate the breadth of imaging applications that we envision SVIM will enable, in capturing tissue-scale 3D dynamic biological systems at single-cell resolution, fast volumetric rates, and high contrast to reveal the underlying biology.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Processamento de Imagem Assistida por Computador / Imageamento Tridimensional Limite: Animals Idioma: En Revista: Commun Biol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Processamento de Imagem Assistida por Computador / Imageamento Tridimensional Limite: Animals Idioma: En Revista: Commun Biol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos