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A xenogeneic-free system generating functional human gut organoids from pluripotent stem cells
Hajime Uchida, Masakazu Machida, Takumi Miura, Tomoyuki Kawasaki, Takuya Okazaki, Kengo Sasaki, Seisuke Sakamoto, Noriaki Ohuchi, Mureo Kasahara, Akihiro Umezawa, Hidenori Akutsu
Hajime Uchida, Masakazu Machida, Takumi Miura, Tomoyuki Kawasaki, Takuya Okazaki, Kengo Sasaki, Seisuke Sakamoto, Noriaki Ohuchi, Mureo Kasahara, Akihiro Umezawa, Hidenori Akutsu
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Resource and Technical Advance Development Stem cells

A xenogeneic-free system generating functional human gut organoids from pluripotent stem cells

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Abstract

Functional intestines are composed of cell types from all 3 primary germ layers and are generated through a highly orchestrated and serial developmental process. Directed differentiation of human pluripotent stem cells (hPSCs) has been shown to yield gut-specific cell types; however, these structures do not reproduce critical functional interactions between cell types of different germ layers. Here, we developed a simple protocol for the generation of mature functional intestinal organoids from hPSCs under xenogeneic-free conditions. The stem cell–derived gut organoids produced here were found to contain distinct types of intestinal cells, including enterocytes, goblet cells, Paneth cells, and enteroendocrine cells, that were derived from all 3 germ layers; moreover, they demonstrated intestinal functions, including peptide absorption, and showed innervated bowel movements in response to stimulation with histamine and anticholinergic drugs. Importantly, the gut organoids obtained using this xenogeneic-free system could be stably maintained in culture for prolonged periods and were successfully engrafted in vivo. Our xenogeneic-free approach for generating gut organoids from hPSCs provides a platform for studying human intestinal diseases and for pharmacological testing.

Authors

Hajime Uchida, Masakazu Machida, Takumi Miura, Tomoyuki Kawasaki, Takuya Okazaki, Kengo Sasaki, Seisuke Sakamoto, Noriaki Ohuchi, Mureo Kasahara, Akihiro Umezawa, Hidenori Akutsu

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Figure 2

Characterization of developing gut organoids.

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Characterization of developing gut organoids.
(A) Analysis of expression...
(A) Analysis of expression of cell biomarker genes in differentiated human embryonic stem cells (hESCs) (SEES1 cells). Values were normalized against GAPDH. The data are reported as mean ± SEM. Statistically significant differences were identified between embryonic stem (ES) vs. day 7, ES vs. day 14, and ES vs. day 21 using Student’s t test (**P < 0.01) (n = 3–6). (B) H&E staining of organoids with peristaltic movement at day 100. Scale bar: 2 mm (left); 200 μm (right). (C) Alcian Blue staining of differentiated organoids (day 60) indicating goblet-like cells (white arrowheads). Scale bar: 100 μm. (D) Relative expression of cell biomarker genes in differentiated day 50 organoids and human adult small intestine. Statistical analysis was performed using a t test or a Mann-Whitney rank-sum test (*P < 0.05, **P < 0.01). The data are reported as means (%) ± SEM and were obtained from 3 independent experiments (n = 3–4).

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