Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, 34141, Republic of Korea.
KRIBB School of Bioscience, Korea University of Science and Technology (UST), Daejeon, 34113, Republic of Korea.
Nat Commun. 2018 Aug 2;9(1):3039. doi: 10.1038/s41467-018-05450-8.
Human pluripotent stem cell (hPSC)-derived intestinal organoids (hIOs) form 3D structures organized into crypt and villus domains, making them an excellent in vitro model system for studying human intestinal development and disease. However, hPSC-derived hIOs still require in vivo maturation to fully recapitulate adult intestine, with the mechanism of maturation remaining elusive. Here, we show that the co-culture with human T lymphocytes induce the in vitro maturation of hIOs, and identify STAT3-activating interleukin-2 (IL-2) as the major factor inducing maturation. hIOs exposed to IL-2 closely mimic the adult intestinal epithelium and have comparable expression levels of mature intestinal markers, as well as increased intestine-specific functional activities. Even after in vivo engraftment, in vitro-matured hIOs retain their maturation status. The results of our study demonstrate that STAT3 signaling can induce the maturation of hIOs in vitro, thereby circumventing the need for animal models and in vivo maturation.
人多能干细胞(hPSC)衍生的肠类器官(hIO)形成 3D 结构,组织成隐窝和绒毛区域,使其成为研究人类肠道发育和疾病的极佳体外模型系统。然而,hPSC 衍生的 hIO 仍需要体内成熟才能完全重现成人肠道,其成熟的机制仍难以捉摸。在这里,我们表明与人 T 淋巴细胞共培养可诱导 hIO 的体外成熟,并鉴定出激活 STAT3 的白细胞介素 2(IL-2)是诱导成熟的主要因素。暴露于 IL-2 的 hIO 与成人肠道上皮细胞非常相似,具有相似水平的成熟肠道标志物,以及增加的肠道特异性功能活性。即使在体内植入后,体外成熟的 hIO 仍保留其成熟状态。我们的研究结果表明,STAT3 信号可以在体外诱导 hIO 的成熟,从而避免了对动物模型和体内成熟的需求。