Human induced pluripotent stem cells (iPSCs) are used in regenerative medicine, disease modelling and drug screening. In addition, organoid culture techniques have enabled investigation of tissue development and cell–cell and tissue–tissue interactions in vitro. Over the past few years, pituitary disease modelling using iPSCs has been developed.
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References
Matsumoto, R. et al. Congenital pituitary hypoplasia model demonstrates hypothalamic OTX2 regulation of pituitary progenitor cells. J. Clin. Invest. 130, 641–654 (2020).
Kanie, K. et al. Modeling of T cell-mediated autoimmune pituitary disease using human induced pluripotent stem cell-originated organoid. Nat. Commun. 16, 7900 (2025).
Suga, H. et al. Self-formation of functional adenohypophysis in three-dimensional culture. Nature 480, 57–62 (2011).
Mac, T. T. et al. Modeling corticotroph deficiency with pituitary organoids supports the functional role of NFKB2 in human pituitary differentiation. eLife 12, RP90875 (2024).
Wang, S. et al. Human pituitary organoids: transcriptional landscape deciphered by scRNA-seq and stereo-seq, with insights into SOX3’s role in pituitary development. Adv. Sci. 12, e2414230 (2025).
Mallick, S. et al. Genetically engineered human pituitary corticotroph tumor organoids exhibit divergent responses to glucocorticoid receptor modulators. Transl. Res. 256, 56–72 (2023).
Matsumoto, R., Suga, H., Arima, H. & Yamamoto, T. Disease modeling of pituitary adenoma using human pluripotent stem cells. Cancers 14, 3660 (2022).
Yamamoto, M. et al. Autoimmune pituitary disease: new concepts with clinical implications. Endocr. Rev. 41, 261–272 (2020).
Urai, S., Iguchi, G. & Takahashi, Y. Anti-PIT1 hypophysitis after immune checkpoint inhibitor treatment. Nat. Rev. Endocrinol. 21, 265–266 (2025).
Leite, N. C. et al. Modeling type 1 diabetes in vitro using human pluripotent stem cells. Cell Rep. 32, 107894 (2020).
Acknowledgements
The authors express their gratitude to T. Aoi, H. Suga, T. Yamamoto, T. Ito, S. Kaneko, S. Urai, G. Iguchi, M. Yamamoto, H. Bando and H. Fukuoka for their insightful advice. The authors acknowledge support from a Grant-in-Aid for Scientific Research from the Japan Society for the Promotion of Science (KAKENHI; 22K16425 to R.M., 22K16396 and 25K19653 to K.K.); a grant from the Ministry of Health, Labor and Welfare (hypothalamo-hypophyseal disorders grant to Y.T.); a Collaborative Research Grant 2025 to Y.T. from the Japan Endocrine Society; and a grant from AMED (Research Center Network for Realization of Regenerative Medicine to Y.T., and JP25ek0109828 to R.M.).
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Matsumoto, R., Kanie, K. & Takahashi, Y. Emerging applications of human iPSCs in pituitary diseases. Nat Rev Endocrinol (2026). https://doi.org/10.1038/s41574-026-01248-7
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DOI: https://doi.org/10.1038/s41574-026-01248-7