Protocol to develop a proximal tubule-on-chip model based on hiPSC-derived kidney organoids for functional analysis of renal transporters
Here, we present a protocol for describing the generation of a proximal tubule-on-chip model using human induced pluripotent stem cell (hiPSC)-derived kidney organoids for renal transporter analysis. We describe steps for hiPSC differentiation into kidney organoids, proximal tubule cell isolation, and microfluidic chip seeding. The hiPSC-derived model enhances transporter expression and polarization, with improved uptake and efflux functions compared to conventional immortalized cell-based models. This protocol serves as a platform to assess renal transporter function, nephrotoxicity, and drug-drug interactions. For complete details on the use and execution of this protocol, please refer to Ma et al.<sup>1</sup>.
Authors
- Cheng Ma (ORCID: https://orcid.org/0000-0002-1569-4987)
- Minoru Takasato (ORCID: https://orcid.org/0000-0002-0458-7414)
- Toshikazu Araoka (ORCID: https://orcid.org/0000-0001-9101-9417)
- Kazuya Fujimoto (ORCID: https://orcid.org/0000-0001-5326-9693)
- Ryosuke Negoro (ORCID: https://orcid.org/0000-0002-6567-575X)
- Ryuji Yokokawa (ORCID: https://orcid.org/0000-0002-6306-2693)
- Ramin Banan Sadeghian (ORCID: https://orcid.org/0000-0003-1695-4477)
- Naoki Ishiguro (ORCID: https://orcid.org/0000-0003-2041-4035)
Institutions
- Ritsumeikan University (JP)
- Kyoto University (JP)
- RIKEN Center for Biosystems Dynamics Research (JP)
- Boehringer Ingelheim (Japan) (JP)
Publication Details
- Journal
- STAR Protocols
- Published
- 2025-04-22
- DOI
- https://doi.org/10.1016/j.xpro.2025.103777
- Primary Topic
- Renal and related cancers
- Type
- article
- Field-Weighted Citation Impact
- 0.00