Methods and systems for converting precursor cells into intestinal tissues through directed differentiation
The generation of complex organ tissues from human embryonic and pluripotent stem cells (PSCs) remains a major challenge for translational studies. It is shown that PSCs can be directed to differentiate into intestinal tissue in vitro by modulating the combinatorial activities of several signaling pathways in a step-wise fashion, effectively recapitulating in vivo fetal intestinal development. The resulting intestinal “organoids” were three-dimensional structures consisting of a polarized, columnar epithelium surrounded by mesenchyme that included a smooth muscle-like layer. The epithelium was patterned into crypt-like SOX9-positive proliferative zones and villus-like structures with all of the major functional cell types of the intestine. The culture system is used to demonstrate that expression of NEUROG3, a pro-endocrine transcription factor mutated in enteric anendocrinosis is sufficient to promote differentiation towards the enteroendocrine cell lineage. In conclusion, PSC-derived human intestinal tissue should allow for unprecedented studies of human intestinal development, homeostasis and disease.
1. A method of inducing formation of an organoid in vitro, wherein said organoid expresses CDX2, KLF5, and SOX9, comprising the steps of:
a) contacting a population of definitive endoderm cells with an FGF signaling pathway activator and a Wnt signaling pathway activator until CDX2+ posterior definitive endoderm cells are obtained, wherein said posterior definitive endoderm cells maintain expression of CDX2 following removal of said FGF signaling pathway activator and said Wnt signaling pathway activator;
b) culturing said posterior definitive endoderm cells of step (a) to obtain a 3-dimensional spheroid, wherein said 3-dimensional spheroid comprises a CDX2+ polarized epithelium and a CDX2+ mesenchyme; and
c) contacting said 3-dimensional spheroid of step (b) with epidermal growth factor (EGF) until said organoid expressing CDX2, KLF5, and SOX9 is obtained.
2. The method of claim 1 , wherein said Wnt signaling pathway activator is one or more molecules selected from Wnt1, Wnt2, Wnt2b, Wnt3, Wnt3a, Wnt4, Wnt5a, Wnt5b, Wnt6, Wnt7a, Wnt7b, Wnt8a, Wnt8b, Wnt9a, Wnt9b, Wnt10a, Wnt10b, Wnt11, Wnt16, Lithium Chloride; 2-amino-4,6-disubstituted pyrimidine (hetero) arylpyrimidines; IQ1; QS11; NSC668036; DCA beta-catenin; 2-amino-4-[3,4-(methylenedioxy)-benzyl -amino]-6-(3-methoxyphenyl) pyrimidine, and combinations thereof.
3. The method of claim 1 , wherein said FGF signaling pathway activator is one or more molecules selected from FGF1, FGF2, FGF3, FGF4, FGF10, FGF11, FGF12, FGF13, FGF14, FGF15, FGF16, FGF17, FGF18, FGF19, FGF20, FGF21, FGF22, and FGF23.
4. The method of claim 1 , wherein said FGF signaling pathway activator is FGF4 and said Wnt signaling pathway activator is Wnt3a.
5. The method of claim 4 , wherein said definitive endoderm cell is contacted by Wnt3a during a first activation period and by FGF4 during a second activation period.
6. The method of claim 5 , wherein said first activation period and said second activation period overlap.
7. The method of claim 5 , wherein said first activation period and said second activation period do not overlap.
8. The method of claim 1 , wherein said specified activation period is between 24 and 120 hours.
9. The method of claim 1 , wherein said population of definitive endoderm cells is contacted with Wnt3a at a concentration between 50-1500 ng/ml.
10. The method of claim 1 , wherein the definitive endoderm cell is derived from a mouse or human pluripotent stem cell.
11. The method of claim 10 , wherein said pluripotent stem cell is an embryonic stem cell, an embryonic stem cell, or an induced pluripotent stem cell.
12. The method of claim 1 , wherein said definitive endoderm cell is derived by contacting the pluripotent stem cell with one or more molecules selected from the group consisting of Activin, the BMP subgroups of the TGF-beta superfamily of growth factors; Nodal, Activin A, Activin B, BMP4, Wnt3a, and a combinations thereof.
13. The method of claim 10 , wherein said pluripotent stem cell is a human pluripotent stem cell.
14. The method of claim 13 , wherein said human pluripotent stem cell is selected from the group consisting of a human embryonic stem cell, a human embryonic germ cell, and an induced human pluripotent stem cell.