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FRaeppli: a multispectral imaging toolbox for cell tracing and dense tissue analysis in zebrafish.
Caviglia, Sara; Unterweger, Iris A; Gasiunaite, Akvile; Vanoosthuyse, Alexandre E; Cutrale, Francesco; Trinh, Le A; Fraser, Scott E; Neuhauss, Stephan C F; Ober, Elke A.
Afiliação
  • Caviglia S; University of Copenhagen, NNF Center for Stem Cell Biology (DanStem), Blegdamsvej 3B, 2200 Copenhagen N, Denmark.
  • Unterweger IA; University of Zurich, Department of Molecular and Life Sciences, Winterthurerstrasse 190, 8057 Zürich, Switzerland.
  • Gasiunaite A; University of Copenhagen, NNF Center for Stem Cell Biology (DanStem), Blegdamsvej 3B, 2200 Copenhagen N, Denmark.
  • Vanoosthuyse AE; University of Copenhagen, NNF Center for Stem Cell Biology (DanStem), Blegdamsvej 3B, 2200 Copenhagen N, Denmark.
  • Cutrale F; University of Copenhagen, NNF Center for Stem Cell Biology (DanStem), Blegdamsvej 3B, 2200 Copenhagen N, Denmark.
  • Trinh LA; Translational Imaging Center, University of Southern California, 1002 West Childs Way, Los Angeles, CA 90089, USA.
  • Fraser SE; Biomedical Engineering, University of Southern California, 1002 West Childs Way, Los Angeles, CA 90089, USA.
  • Neuhauss SCF; Translational Imaging Center, University of Southern California, 1002 West Childs Way, Los Angeles, CA 90089, USA.
  • Ober EA; Molecular and Computational Biology, University of Southern California, 1002 West Childs Way, Los Angeles, CA 90089, USA.
Development ; 149(16)2022 08 15.
Article em En | MEDLINE | ID: mdl-35980363
ABSTRACT
Visualizing cell shapes and interactions of differentiating cells is instrumental for understanding organ development and repair. Across species, strategies for stochastic multicolour labelling have greatly facilitated in vivo cell tracking and mapping neuronal connectivity. Yet integrating multi-fluorophore information into the context of developing zebrafish tissues is challenging given their cytoplasmic localization and spectral incompatibility with common fluorescent markers. Inspired by Drosophila Raeppli, we developed FRaeppli (Fish-Raeppli) by expressing bright membrane- or nuclear-targeted fluorescent proteins for efficient cell shape analysis and tracking. High spatiotemporal activation flexibility is provided by the Gal4/UAS system together with Cre/lox and/or PhiC31 integrase. The distinct spectra of the FRaeppli fluorescent proteins allow simultaneous imaging with GFP and infrared subcellular reporters or tissue landmarks. We demonstrate the suitability of FRaeppli for live imaging of complex internal organs, such as the liver, and have tailored hyperspectral protocols for time-efficient acquisition. Combining FRaeppli with polarity markers revealed previously unknown canalicular topologies between differentiating hepatocytes, reminiscent of the mammalian liver, suggesting common developmental mechanisms. The multispectral FRaeppli toolbox thus enables the comprehensive analysis of intricate cellular morphologies, topologies and lineages at single-cell resolution in zebrafish.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peixe-Zebra / Integrases Limite: Animals Idioma: En Revista: Development Assunto da revista: BIOLOGIA / EMBRIOLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Dinamarca

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peixe-Zebra / Integrases Limite: Animals Idioma: En Revista: Development Assunto da revista: BIOLOGIA / EMBRIOLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Dinamarca