Kidney micro-organoids in suspension culture as a scalable source of human pluripotent stem cell-derived kidney cells

  • Santhosh V. Kumar
    Murdoch Children's Research Institute 1 , Flemington Rd, Parkville, Victoria 3052 , Australia
  • Pei X. Er
    Murdoch Children's Research Institute 1 , Flemington Rd, Parkville, Victoria 3052 , Australia
  • Kynan T. Lawlor
    Murdoch Children's Research Institute 1 , Flemington Rd, Parkville, Victoria 3052 , Australia
  • Ali Motazedian
    Murdoch Children's Research Institute 1 , Flemington Rd, Parkville, Victoria 3052 , Australia
  • Michelle Scurr
    Murdoch Children's Research Institute 1 , Flemington Rd, Parkville, Victoria 3052 , Australia
  • Irene Ghobrial
    Murdoch Children's Research Institute 1 , Flemington Rd, Parkville, Victoria 3052 , Australia
  • Alexander N. Combes
    Murdoch Children's Research Institute 1 , Flemington Rd, Parkville, Victoria 3052 , Australia
  • Luke Zappia
    Murdoch Children's Research Institute 1 , Flemington Rd, Parkville, Victoria 3052 , Australia
  • Alicia Oshlack
    Murdoch Children's Research Institute 1 , Flemington Rd, Parkville, Victoria 3052 , Australia
  • Edouard G. Stanley
    Murdoch Children's Research Institute 1 , Flemington Rd, Parkville, Victoria 3052 , Australia
  • Melissa H. Little
    Murdoch Children's Research Institute 1 , Flemington Rd, Parkville, Victoria 3052 , Australia

抄録

<jats:title>ABSTRACT</jats:title> <jats:p>Kidney organoids have potential uses in disease modelling, drug screening and regenerative medicine. However, novel cost-effective techniques are needed to enable scaled-up production of kidney cell types in vitro. We describe here a modified suspension culture method for the generation of kidney micro-organoids from human pluripotent stem cells. Optimisation of differentiation conditions allowed the formation of micro-organoids, each containing six to ten nephrons that were surrounded by endothelial and stromal populations. Single cell transcriptional profiling confirmed the presence and transcriptional equivalence of all anticipated renal cell types consistent with a previous organoid culture method. This suspension culture micro-organoid methodology resulted in a three- to fourfold increase in final cell yield compared with static culture, thereby representing an economical approach to the production of kidney cells for various biological applications.</jats:p>

収録刊行物

  • Development

    Development 146 (5), dev172361-, 2019-03-01

    The Company of Biologists

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