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Method Article

Technique to Target Microinjection to the Developing Xenopus Kidney

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DOI:

10.3791/53799

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May 3rd, 2016

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In This Article

Summary

Here, we present a protocol to use fate maps and lineage tracers to target injections into individual blastomeres that give rise to the kidney of Xenopus laevis embryos.

Abstract

The embryonic kidney of Xenopus laevis (frog), the pronephros, consists of a single nephron, and can be used as a model for kidney disease. Xenopus embryos are large, develop externally, and can be easily manipulated by microinjection or surgical procedures. In addition, fate maps have been established for early Xenopus embryos. Targeted microinjection into the individual blastomere that will eventually give rise to an organ or tissue of interest can be used to selectively overexpress or knock down gene expression within this restricted region, decreasing secondary effects in the rest of the developing embryo. In this protocol, we describe how to utilize established Xenopus fate maps to target the developing Xenopus kidney (the pronephros), through microinjection into specific blastomere of 4- and 8-cell embryos. Injection of lineage tracers allows verification of the specific targeting of the injection. After embryos have developed to stage 38 - 40, whole-mount immunostaining is used to visualize pronephric development, and the contribution by targeted cells to the pronephros can be assessed. The same technique can be adapted to target other tissue types in addition to the pronephros.

Introduction

The Xenopus embryonic kidney, the pronephros, is a good model for studying kidney development and disease. The embryos develop externally, are large in size, can be produced in large numbers, and are easily manipulated through microinjection or surgical procedures. In addition, the genes governing kidney development in mammals and amphibians are conserved. Mammalian kidneys progress through three stages: the pronephros, mesonephros, and metanephros1, while embryonic amphibians have a pronephros and adult amphibians have a metanephros. The basic filtering unit of these kidney forms is the nephron, and both mammals and amphibians require the same sig....

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Protocol

The following protocol has been approved by the University of Texas Health Science Center at Houston's Center for Laboratory Animal Medicine Animal Welfare Committee, which serves as the Institutional Care and Use Committee (protocol #: HSC-AWC-13-135).

1. Identification and Selection of Blastomeres for Kidney-targeted Injections 

  1. Prior to generating embryos, use the Normal Table of Xenopus Development21 to understand the orientation of the early cell divisions in the embryo. Alternatively, access diagrams of the early developmental stages of Xenopus on Xenbase11.
  2. Access the interactive ....

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Results

Microinjections of 4- and 8-cell Xenopus embryos with MEM-RFP mRNA show different levels of targeting to the pronephros. Figure 4 shows stage 40 embryos with correct MEM-RFP mRNA expression patterns. Embryos were injected in the left ventral blastomere (Figure 4A), and sorted for the proper expression pattern of MEM-RFP mRNA. In addition to expressing MEM-RFP in the proximal, intermediate, distal and connecting tubules of the kidney, properly inj.......

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Discussion

Targeting the pronephros of developing Xenopus embryos relies on identifying and injecting the correct blastomere. Injection of the V2 blastomere of 8-cell embryos targets the left pronephros18. This leaves the contralateral right pronephros as an internal control. If morpholino knockdown or RNA overexpression is used to alter kidney development, the contralateral right pronephros can be used to compare the effects of gene knockdown or overexpression on the left pronephros. In this case, proper contro.......

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Disclosures

The authors declare that they have no competing financial interests.

Acknowledgements

This work was supported by a National Institutes of Health NIDDK grant (K01DK092320) and startup funding from the Department of Pediatrics at the University of Texas McGovern Medical School.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Sodium chlorideFisherS271-3
Potassium chlorideFisherP217-500
Magnesium sulfate FisherM63-500
Calcium chlorideFisherC79-500
HEPESFisherBP310-500
EDTAFisherS311-500
Gentamycin solution, 50 mg/mlAmrescoE737-20ML
L-Cysteine, 99%+Acros Organics52-90-4
FicollFisherBP525-100
100 mm x 15 mm Petri dishFisherFB0875712
Mini Fridge IIBoekel260009Benchtop incubator for embryos.
Gap43-RFP plasmidFor making tracer RNA. Ref: Davidson et al., 2006.
Rhodamine dextran, 10,000 M.W.InvitrogenD1817Tracer.
Molecular biology grade, USP sterile purified waterCorning46-000-CI
7" Drummond replacement tubesDrummond3-000-203-G/XLMicroinjection needles.
Needle pullerSutter InstrumentsP-30
Fine forcepsDumont11252-30For breaking microinjection needle tip.
Nanoject IIDrummond3-000-204Microinjector.
Mineral oil, heavyFisherCAS 8042-47-5Oil for needles.
27 G Monoject hypodermic needleCovidien8881200508For loading mineral oil into microinjection needle.
5 ml Luer-Lok syringeBD309646For loading mineral oil into microinjection needle.
60 mm x 15 mm Petri dishFisherFB0875713A
800 micron Polyester meshSmall PartsCMY-0800-C
Transfer pipetsFisher13-711-7MFor transferring embryos. Cut off the tip so that the embryos are easily taken up by the pipette.
6-well cell culture plateNest Biotechnology
MOPSFisherBP308-500
EGTAAcros Organics67-42-5
FormaldehydeFisherBP531-500
15 mm x 45 mm Screw thread vialFisher03-339-25BFor fixing, staining, and storing embryos.
24-well cell Culture plateNest Biotechnology
BenzocaineSpectrumBE130
EthanolFisherBP2818-4
MethanolFisherA412-4
Phosphate buffered saline (PBS) 1x powderFisherBP661-50
Bovine serum albumenFisherBP1600-100
Triton X-100FisherBP151-500
3D Mini rocker, model 135Denville Scientific57281
Goat serum, New Zealand originInvitrogen16210064
Sodium azideFisherS227I-25
Monoclonal 3G8 antibodyEuropean Xenopus Resource CentrePrimary antibody to label proximal tubules.
Monoclonal 4A6 antibodyEuropean Xenopus Resource CentrePrimary antibody to label intermediate, distal and connecting tubules.
anti-RFP pAb, purified IgG/rabbitMBLPM005Primary antibody to label Gap43-RFP tracer.
Alexa Fluor 488 goat anti-mouse IgGLife TechnologiesA11001Secondary antibody to label kidney tubules.
Alexa Fluor 555 goat anti-rabbit IgGLife TechnologiesA21428Secondary antibody to label Gap43-RFP tracer.
9 Cavity spot plateCorning7220-85
Benzyl benzoateFisher105862500Optional - for clearing embryos
Benzyl alcoholFisherA396-500Optional - for clearing embryos

References

  1. Vize, P. D., Seufert, D. W., Carroll, T. J., Wallingford, J. B. Model systems for the study of kidney development: Use of the pronephros in the analysis of organ induction and patterning. Dev. Biol. 188 (2), 189-204 (1997).
  2. Brandli, A. W.

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