Literature DB >> 34244350

Imaging Methods in Xenopus Cells, Embryos, and Tadpoles.

Lance A Davidson1, Laura Anne Lowery2.   

Abstract

Xenopus is an excellent vertebrate model system ideally suited for a wide range of imaging methods designed to investigate cell and developmental biology processes. The individual cells of Xenopus are much larger than those in many other vertebrate model systems, such that both cell behavior and subcellular processes can more easily be observed and resolved. Gene function in Xenopus can be manipulated and visualized using a variety of approaches, and the embryonic fate map is stereotypical, such that microinjections can target specific tissues and cell types during development. Tissues, organotypic explants, and individual cells can also be mounted in stable chambers and cultured easily in simple salt solutions without cumbersome environmental controls. Furthermore, Xenopus embryonic tissues can be microsurgically isolated and shaped to expose cell behaviors and protein dynamics in any regions of the embryo to high-resolution live-cell imaging. The combination of these attributes makes Xenopus a powerful system for understanding cell and developmental processes as well as disease mechanisms, through quantitative analysis of protein dynamics, cell movements, tissue morphogenesis, and regeneration. Here, we introduce various methods, of both fixed and living tissues, for visualizing Xenopus cells, embryos, and tadpoles. Specifically, we highlight protocol updates for whole-mount in situ hybridization and immunofluorescence, as well as robust live imaging approaches including methods for optimizing the time-lapse imaging of whole embryos and explants.
© 2022 Cold Spring Harbor Laboratory Press.

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Year:  2022        PMID: 34244350      PMCID: PMC9476831          DOI: 10.1101/pdb.top105627

Source DB:  PubMed          Journal:  Cold Spring Harb Protoc        ISSN: 1559-6095


  26 in total

1.  Multichannel wholemount fluorescent and fluorescent/chromogenic in situ hybridization in Xenopus embryos.

Authors:  Peter D Vize; Kyle E McCoy; Xiaolan Zhou
Journal:  Nat Protoc       Date:  2009       Impact factor: 13.491

2.  Magnetic resonance microscopy of embryonic cell lineages and movements.

Authors:  R E Jacobs; S E Fraser
Journal:  Science       Date:  1994-02-04       Impact factor: 47.728

3.  Vital dye mapping of the gastrula and neurula of Xenopus laevis. II. Prospective areas and morphogenetic movements of the deep layer.

Authors:  R E Keller
Journal:  Dev Biol       Date:  1976-07-01       Impact factor: 3.582

4.  Imaging developing neural morphology using optical coherence tomography.

Authors:  S A Boppart; B E Bouma; M E Brezinski; G J Tearney; J G Fujimoto
Journal:  J Neurosci Methods       Date:  1996-12       Impact factor: 2.390

5.  Low-magnification live imaging of Xenopus embryos for cell and developmental biology.

Authors:  John B Wallingford
Journal:  Cold Spring Harb Protoc       Date:  2010-05

Review 6.  Tools for live imaging of active Rho GTPases in Xenopus.

Authors:  Rachel E Stephenson; Ann L Miller
Journal:  Genesis       Date:  2017-01       Impact factor: 2.487

7.  Neurulation in Xenopus laevis. An analysis and model based upon light and electron microscopy.

Authors:  T E Schroeder
Journal:  J Embryol Exp Morphol       Date:  1970-04

8.  The neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and control of brain size in Xenopus embryos.

Authors:  Helen Rankin Willsey; Yuxiao Xu; Amanda Everitt; Jeanselle Dea; Cameron R T Exner; A Jeremy Willsey; Matthew W State; Richard M Harland
Journal:  Development       Date:  2020-06-22       Impact factor: 6.868

9.  X-ray phase-contrast in vivo microtomography probes new aspects of Xenopus gastrulation.

Authors:  Julian Moosmann; Alexey Ershov; Venera Altapova; Tilo Baumbach; Maneeshi S Prasad; Carole LaBonne; Xianghui Xiao; Jubin Kashef; Ralf Hofmann
Journal:  Nature       Date:  2013-05-16       Impact factor: 49.962

10.  Neural tube closure in Xenopus laevis involves medial migration, directed protrusive activity, cell intercalation and convergent extension.

Authors:  L A Davidson; R E Keller
Journal:  Development       Date:  1999-10       Impact factor: 6.868

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