Evaluation of the ability of human induced nephron progenitor cells to form chimeric renal organoids using mouse embryonic renal progenitor cells

• Published in: Biochemical and biophysical research communications 2023-06, Vol.662, p.18-25
• Main Authors: Matsumoto, Naoto, Yamanaka, Shuichiro, Morimoto, Keita, Matsui, Kenji, Nishimura, Sandy, Kinoshita, Yoshitaka, Inage, Yuka, Fujimori, Koki, Kuroda, Takao, Saito, Yatsumu, Takamura, Tsuyoshi, Fujimoto, Toshinari, Tajiri, Susumu, Matsumoto, Kei, Inoue, Makoto, Kobayashi, Eiji, Yokoo, Takashi
• Format: Article
• Language: English
• Subjects: Animals; Cell Differentiation; Chimera; Embryonic Stem Cells; Humans; Kidney; Mice; Mice, Transgenic; Nephrons; Organoid; Organoids; Progenitors; Regeneration; Xenotransplantation
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2023.04.052

The number of patients with end-stage renal failure is increasing annually worldwide and the problem is compounded by a shortage of renal transplantation donors. In our previous research, we have shown that transplantation of renal progenitor cells into the nephrogenic region of heterologous fetuses can induce the development of nephrons. We have also developed transgenic mice in which specific renal progenitor cells can be removed by drugs. By combining these two technologies, we have succeeded in generating human-mouse chimeric kidneys in fetal mice. We hope to apply these technologies to regenerative medicine. The quality of nephron progenitor cells (NPCs) derived from human pluripotent stem cells is important for the generation of chimeric kidneys, but there is currently no simple evaluation system for the chimerogenic potential of human NPCs. In this study, we focused on the fact that the re-aggregation of mouse renal progenitor cells can be used for nephron formation, even when merged into single cells. First, we examined the conditions under which nephron formation is likely to occur in mice during re-aggregation. Next, to improve the differentiation potential of human NPCs derived from pluripotent stem cells, NPCs were sorted using Integrin subunit alpha 8 (ITGA8). Finally, we demonstrated chimera formation between different species by mixing mouse cells with purified, selectively-induced human NPCs under optimum conditions. We observed these chimeric organoids at different time points to learn about these human-mouse chimeric structures at various stages of renal development. We found that the rate of chimera formation was affected by the purity of the human NPCs and the cell ratios used. We demonstrated that chimeric nephrons can be generated using a simple model, even between distant species. We believe that this admixture of human and mouse renal progenitor cells is a promising technology with potential application for the evaluation of the chimera formation abilities of NPCs. •Renal chimeric organoids were created by mixing human nephron progenitor cells (NPCs) with mouse renal progenitor cells.•Human-mouse kidney chimeric organoids showed chimeric structures at various stages of renal development.•The rate of chimera formation was affected by the cell admixture ratio and the purity of NPCs.