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In This Article

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

Summary

Here we describe a protocol to generate kidney organoids from human pluripotent stem cells (hPSCs). This protocol generates kidney organoids within two weeks. The resulting kidney organoids can be cultured in large-scale spinner flasks or multi-well magnetic stir plates for parallel drug-testing approaches.

Abstract

Kidney organoids generated from hPSCs have provided an unlimited source of renal tissue. Human kidney organoids are an invaluable tool for studying kidney disease and injury, developing cell-based therapies, and testing new therapeutics. For such applications, large numbers of uniform organoids and highly reproducible assays are needed. We have built upon our previously published kidney organoid protocol to improve the overall health of the organoids. This simple, robust 3D protocol involves the formation of uniform embryoid bodies in minimum component medium containing lipids, insulin-transferrin-selenium-ethanolamine supplement and polyvinyl alcohol with GSK3 inhibitor (CHIR99021) for 3 days, followed by culture in knock-out serum replacement (KOSR)-containing medium. In addition, agitating assays allows for reduction in clumping of the embryoid bodies and maintaining a uniform size, which is important for reducing variability between organoids. Overall, the protocol provides a fast, efficient, and cost-effective method for generating large quantities of kidney organoids.

Introduction

In recent years, a number of protocols to differentiate human pluripotent stem cells into kidney organoids have been developed1,2,3,4,5. Kidney organoids have provided an important tool to aid research into new regenerative medicine approaches, model kidney-related diseases, perform toxicity studies and therapeutic drug development. Despite their wide applicability, kidney organoids have limitations such as lack of maturation, limited long-term culture capacity in vitro, and a paucity of several ce....

Protocol

All experiments using hPSCs were performed in compliance with institutional guidelines, and were carried out in a Class II biosafety hood with appropriate personal protective equipment. All reagents are cell culture-grade unless stated otherwise. All cultures are incubated at 37 °C, 5% CO2 air atmosphere. At all stages of the assay, embryoid bodies or kidney organoids can be collected, and fixed or prepared for analysis. The hPSC lines used to generate this data have been fully characterized and published18.

1. Preparing culture plates

NOTE: Approximately 1 h prior to splitti....

Results

In this most recent version of our protocol, kidney organoid differentiation is initiated in a defined, low protein medium. The assays are performed entirely in suspension and rely on the innate ability of hPSCs differentiation and organization for initiation of tubulogenesis. A single assay originating from a 100 mm ~60% confluent hPSC culture plate routinely yields 500-1,000 kidney organoids, as shown in our previous publication5. Due to such high numbers of organoids generated, this protocol is.......

Discussion

Previous studies have shown that the initial protocol steps are critical for intermediate mesoderm differentiation5,19,20 and, therefore, it is essential to implement a stringent medium composition at this stage. Removing undefined components such as serum, albumin, protein free hybridoma medium II from the first stage of the protocol may help to improve consistent differentiation efficiency between assays21

Disclosures

Authors have nothing to disclose.

Acknowledgements

This research was funded by the National Institutes of Health R01 DK069403, UC2 DK126122 and P30-DK079307 and ASN Foundation for Kidney Research Ben J. Lipps Research Fellowship Program to AP.

....

Materials

NameCompanyCatalog NumberComments
2-MercaptoethanolThermo Fisher21-985-023
Anti-adherence rinsing solutionSTEMCELL Technologies7010
CHIR99021STEMCELL Technologies7205410 mM stock in DMSO
Corning disposable spinner flasksFisher Scientific07-201-152
Corning Ultra-Low Attachment 6-well platesFisher Scientific07-200-601
Corning Slow-Speed StirrersFisher Scientific11-495-03Multi plate magnetic stirrer for spinner flask culture
DispaseSTEMCELL Technologies7923Aliquot and freeze
DMEM, low glucose, pyruvate, no glutamine, no phenol redThermo Fisher11054020
DPBS 1x, no calcium, no magnesiumThermo Fisher14-190-250
Egg / Oval Stirring Bars2magPI20106
Excelta General-Purpose TweezersFisher Scientific17-456-103Keep sterile in the cell culture hood
EZBio Single Use Media Bottle, 250mLFoxx Life Sciences138-3211-FLSUsed to make PVA 10%
Falcon Standard Tissue Culture Dishes (100 mm)Thermo Fisher08-772E
Fisherbrand Sterile Aspirating Pipet 2mLFisher Scientific14-955-135
Fisherbrand  Cell Lifters - Cell lifterFisher Scientific08-100-240
Fisherbrand Multi Function 3D RotatorsFisher Scientific88-861-047Orbital shaker
Geltrex LDEV-Free Reduced Growth Factor Basement Membrane MatrixThermo FisherA1413302BME. Aliquot on ice and freeze. Another suitable matrix alternative is Matrigel or Cultrex.
Gentle Cell Dissociation ReagentSTEMCELL Technologies7174GCDR
GlutaMAX SupplementThermo Fisher35-050-061L-glutamine supplement.
HEPES (1M)Thermo Fisher15-630-080
Insulin-Transferrin-Selenium-EthanolamineThermo Fisher51-500-056ITSE
KnockOut  Serum Replacement - Multi-SpeciesThermo FisherA3181502KOSR. Aliquot and freeze
Lipid Mixture 1, Chemically DefinedMillipore-SigmaL0288-100ML
MEM Non-Essential Amino Acids SolutionThermo Fisher11140-050
MilliporeSigma Stericup Quick Release-GP Sterile Vacuum Filtration System 500mLFisher ScientificS2GPU05RE
MilliporeSigma  Stericup Quick Release-GP Sterile Vacuum Filtration System 250mLFisher ScientificS2GPU02RE
MIXcontrol MTP / Variomag TELEcontrol MTP Control Unit2magVMF 90250 U
MIXdrive 6 MTP / Variomag TELEdrive 6 MTP Microplate Stirring Drive2magVMF 406006MSP
MP Biomedicals  7X Cleaning SolutionFisher ScientificMP0976670A4Tissue culture suitable detergent. Make a 5% solution in water
mTeSR1STEMCELL Technologies85850hPSC medium.TeSR-E8, NutriStem XF, and mTeSR Plus medium have also been tested and are suitable alternatives. 
Nunc 50 mL Conical, Sterile Centrifuge TubesFisher Scientific12-565-270
Nunc 15mL Conical Sterile Centrifuge TubesFisher Scientific12-565-268
Penicillin-StreptomycinThermo Fisher15-140-122Aliquot and freeze
PlasmocinInvivogenant-mptAnti-mycoplasma reagent. Aliquot and freeze
pluriStrainer® 200 µmFisher ScientificNC0776417Cell strainer
pluriStrainer® 500 µmFisher ScientificNC0822591Cell strainer
Poly(vinyl alcohol) 87-90% hydrolyzed  (PVA)Millipore-SigmaP8136-250G10% in DPBS stirring at 98 degrees C until disolves, make in 138-3211-FLS
ROCK inhibitor Y-27632 (ROCKi)STEMCELL Technologies7230410 mM stock in DPBS
Sterile Disposable Serological Pipets  - 10mLFisher Scientific13-678-11E
Sterile Disposable Serological Pipets - 25mLFisher Scientific13-678-11
Sterile Disposable Serological pipette - 5 mLFisher Scientific13-678-12D
TeSR-E5STEMCELL Technologies5916Serum-free, low protein base medium for E5-ILP
Variomag distriBOX 2 Distributor2magVMF 90512If you use more than one MIXdrive

References

  1. Takasato, M., et al. Kidney organoids from human iPS cells contain multiple lineages and model human nephrogenesis. Nature. 526 (7574), 564-568 (2015).
  2. Freedman, B. S., et al.

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Kidney OrganoidsHuman Pluripotent Stem CellsHPSCsCell CultureRenal DevelopmentRenal DiseaseSimplified MethodCell DifferentiationEmbryoid BodiesCell Culture Techniques

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