| Literature DB >> 29470983 |
Yoshiyuki Saito1, Nobuyuki Onishi2, Hiroshi Takami3, Ryo Seishima4, Hiroyoshi Inoue5, Yuki Hirata1, Kaori Kameyama6, Kenji Tsuchihashi2, Eiji Sugihara2, Shinya Uchino7, Koichi Ito3, Hirofumi Kawakubo8, Hiroya Takeuchi9, Yuko Kitagawa8, Hideyuki Saya2, Osamu Nagano10.
Abstract
The low turnover rate of thyroid follicular cells and the lack of a long-term thyroid cell culture system have hampered studies of thyroid carcinogenesis. We have now established a thyroid organoid culture system that supports thyroid cell proliferation in vitro. The established mouse thyroid organoids performed thyroid functions including thyroglobulin synthesis, iodide uptake, and the production and release of thyroid hormone. Furthermore, transplantation of the organoids into recipient mice resulted in the formation of normal thyroid-like tissue capable of iodide uptake and thyroglobulin production in vivo. Finally, forced expression of oncogenic NRAS (NRASQ61R) in thyroid organoids established from p53 knockout mice and transplantation of the manipulated organoids into mouse recipients generated a model of poorly differentiated thyroid cancer. Our findings suggest that this newly developed thyroid organoid culture system is a potential research tool for the study of thyroid physiology and pathology including thyroid cancer.Entities:
Keywords: NRAS; Organoid; Thyroid; Thyroid cancer model; p53
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Year: 2018 PMID: 29470983 DOI: 10.1016/j.bbrc.2018.02.154
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575