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A xenogeneic-free system generating functional human gut organoids from pluripotent stem cells
Hajime Uchida, … , Akihiro Umezawa, Hidenori Akutsu
Hajime Uchida, … , Akihiro Umezawa, Hidenori Akutsu
Published January 12, 2017
Citation Information: JCI Insight. 2017;2(1):e86492. https://doi.org/10.1172/jci.insight.86492.
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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 4

Contractility of gut organoids.

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Contractility of gut organoids.
(A) Immunohistochemical staining for α-s...
(A) Immunohistochemical staining for α-smooth muscle actin (SMA) in a day 60 gut organoid. Scale bar: 200 μm. (B) Immunostaining for the intestinal cells of Cajal. CKIT and S-100 double-positive cells within the myenteric and submucosal plexuses (white arrowheads). Scale bar: 50 μm. (C) The distribution of the neurotransmitter serotonin, an enteroendocrine cell marker, in a representative hESC-derived day 60 gut organoid. Serotonin-positive cells were observed in the lining epithelium and displayed a triangular shape (yellow arrowheads). Scale bar: 100 μm. (D) Contractile activity of the motile gut organoid in response to pharmacological agents (Supplemental Video 2). The aspect ratios are based on the ratio of the longest diameter to the shortest diameter of the organoid, which were calculated for each frame. The original video was recorded at 30 frames per second. The playback speed of the video was 20 times actual speed. Waves of constant contractions were observed before treatment (frames 1–160), histamine treatment increased the frequency of gut organoid contractile activity in frequency, and atropine treatment decreased contraction amplitude and frequency. (E) Nonmotile organoids (n = 6) did not show contractions in response to histamine (Supplemental Video 3). The original video was recorded at 30 frames per second. (F) Human intestine tissue and motile and nonmotile organoids were immunostained for histamine H1 receptor. Cell nuclei were counterstained with DAPI. Nonmotile organoids showed positive staining in the epithelial and mesenchymal areas. Scale bar: 20 μm.

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