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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

This article presents a guide for sampling six significant and diverse organs in adult Xenopus that can be rapidly and easily accessed: the heart ventricle, liver lobe, pancreas, fat bodies, paired kidneys, and skin.

Abstract

Xenopus has been a powerful model organism for understanding vertebrate development and disease for over a hundred years. While experimental analysis and dissection techniques of the embryo have been well documented, descriptions of adult Xenopus structures and organs, together with techniques for working with adults, have not been updated to take into consideration the requirements of such modern approaches as quantitative proteomics and single-cell transcriptomics. The cell-type and gene-centric perspectives require contrasting observations in embryonic stages to those in adult tissues. The organs of the larva undergo significant changes in their overall structure, morphology, and anatomical location all along the larval to adult transition, most notably during massive metamorphosis remodeling. Establishing robust standards for organ identification and dissection is crucial to ensure datasets resulting from studies performed at different laboratories can be consistent. The present protocol identifies six of the organs in the adult Xenopus, demonstrating methods for dissection and sampling of the heart ventricle, liver, fat body, pancreas, paired kidney, and skin of the adult Xenopus. Depending on the preservation methods, the dissected organs can be used for quantitative proteomics, single cell/nuclei transcriptomics, in situ hybridization, immunohistochemistry, histology, etc. This protocol aims to standardize tissue sampling and facilitate multi-lab investigations of the adult organ systems.

Introduction

Though the "digital dissection" of adult Xenopus” is available1, replicable organ and tissue sampling of adult Xenopus remains challenging without the detailed instruction available for other adult models (e.g. mice2,3,4). This article aims to provide clear guidance for accurate and replicable organ sampling of adult Xenopus similar to what is currently available for their larvae5. An emphasis is placed on ease of completion to maintain maximum freshness and make the protocol accessible t....

Protocol

All experiments were performed in accordance with the rules and regulations of the Harvard Medical School IACUC (Institutional Animal Care and Use Committee) (IS 00001365_3). The representative results are shown for both a perfused and unperfused mature albino male Xenopus laevis.

1. Experimental preparation

NOTE: If perfusion protocol8 is being followed before sampling, skip to step 2.2.

  1. Ensure that the.......

Representative Results

By utilizing Figure 1 to Figure 20 and following all steps of this protocol, the heart ventricle, the left lobe of the liver, the pancreas, the left fat bodies, paired kidneys, and a flap of skin were cleanly excised within an hour of euthanasia. Within this time, the samples are rinsed and trimmed so that they will appear, as shown in Figure 21.

Discussion

As this protocol aims to maximize freshness, some samples may include undesired tissues. For example, the hepatopancreatic duct and some mesentery are sampled with the pancreas, and some peritoneal tissue, adrenal glands, and ureters will always be sampled with the paired kidneys.  If freshness is not a concern, then more precise sampling can be achieved using modified techniques.

The appearance and location of organs are comparable between sexes and species of Xenopus. However, .......

Acknowledgements

This work was supported by NIH's OD grant R24OD031956. We thank Samantha Jalbert, Jill Ralston, and Cora Anderson for their assistance and support as well as our editor and anonymous peer reviewers for their helpful feedback

....

Materials

NameCompanyCatalog NumberComments
5x Magnifying Glass with LED Light and Standamazon.comB08QJ6J8P1light must not produce heat
Disposable Transfer PipetsVWR414004-036
Dissecting Fine-Pointed ForcepsFisher Scinetific08-875
Dissecting scissors sharp piont, straight 6.5"VWR76457-374
Dissection TrayFisher Scinetific14-370-284styrofoam sheets are an acceptable alternative
Euthanasia containerUS Plastic Item 2860alternative opaque containers acceptable
Euthanasia container lidUS Plastic Item 3047
Iridectomy Scissors 6"vwr470018-938iris scissors are an acceptable alternative
MS-222: Syncaine (formerly tricaine)Pentair AESTRS1
PBS 1xCorning21-040-CV
Sodium Bicarbonate, Powder, USPFisher Scientific18-606-333
Specimen Forceps, SerratedVWR82027-442
T-Pins for DissectingFisher ScinetificS99385

References

  1. Porro, L. B., Richards, C. T. Digital dissection of the model organism Xenopus laevis using contrast-enhanced computed tomography. J Anat. 231 (2), 169-191 (2017).
  2. Ruehl-Fehlert, C., et al.

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Organ DissectionXenopusAdult Tissue SamplingHeart VentricleLiverFat BodyPancreasKidneySkinProteomicsTranscriptomicsHistology

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