Human Intestinal Tissue with Adult Stem Cell Properties Derived from Pluripotent Stem Cells

Ryan Forster(University of California, Berkeley), Kunitoshi Chiba(University of California, Berkeley), Lorian Schaeffer(University of California, Berkeley), Samuel G. Regalado(University of California, Berkeley), Christine S. Lai(Whitehead Institute for Biomedical Research), Qing Gao(Whitehead Institute for Biomedical Research), Samira Kiani(Whitehead Institute for Biomedical Research), Henner F. Farin(Royal Netherlands Academy of Arts and Sciences), Hans Clevers(Skolkovo Institute of Science and Technology), Gregory J. Cost(Sangamo BioSciences (United States)), Andy Chan(Sangamo BioSciences (United States)), Edward J. Rebar(Sangamo BioSciences (United States)), Fyodor D. Urnov(Sangamo BioSciences (United States)), Philip D. Gregory(Sangamo BioSciences (United States)), Lior Pachter(University of California, Berkeley), Rudolf Jaenisch(Skolkovo Institute of Science and Technology), Dirk Hockemeyer(University of California, Berkeley)
Stem Cell Reports
June 1, 2014
Cited by 88Open Access
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Abstract

Genetically engineered human pluripotent stem cells (hPSCs) have been proposed as a source for transplantation therapies and are rapidly becoming valuable tools for human disease modeling. However, many applications are limited due to the lack of robust differentiation paradigms that allow for the isolation of defined functional tissues. Here, using an endogenous LGR5-GFP reporter, we derived adult stem cells from hPSCs that gave rise to functional human intestinal tissue comprising all major cell types of the intestine. Histological and functional analyses revealed that such human organoid cultures could be derived with high purity and with a composition and morphology similar to those of cultures obtained from human biopsies. Importantly, hPSC-derived organoids responded to the canonical signaling pathways that control self-renewal and differentiation in the adult human intestinal stem cell compartment. This adult stem cell system provides a platform for studying human intestinal disease in vitro using genetically engineered hPSCs.


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