| Literature DB >> 34582804 |
Wei Gu1, Hua Wang2, Xiaofeng Huang1, Judith Kraiczy3, Pratik N P Singh3, Charles Ng4, Sezin Dagdeviren5, Sean Houghton1, Oscar Pellon-Cardenas6, Ying Lan1, Yaohui Nie1, Jiaoyue Zhang1, Kushal K Banerjee3, Emily J Onufer7, Brad W Warner7, Jason Spence8, Ellen Scherl4, Shahin Rafii1, Richard T Lee5, Michael P Verzi6, David Redmond1, Randy Longman4, Kristian Helin9, Ramesh A Shivdasani3, Qiao Zhou10.
Abstract
Adult stem cells maintain regenerative tissue structure and function by producing tissue-specific progeny, but the factors that preserve their tissue identities are not well understood. The small and large intestines differ markedly in cell composition and function, reflecting their distinct stem cell populations. Here we show that SATB2, a colon-restricted chromatin factor, singularly preserves LGR5+ adult colonic stem cell and epithelial identity in mice and humans. Satb2 loss in adult mice leads to stable conversion of colonic stem cells into small intestine ileal-like stem cells and replacement of the colonic mucosa with one that resembles the ileum. Conversely, SATB2 confers colonic properties on the mouse ileum. Human colonic organoids also adopt ileal characteristics upon SATB2 loss. SATB2 regulates colonic identity in part by modulating enhancer binding of the intestinal transcription factors CDX2 and HNF4A. Our study uncovers a conserved core regulator of colonic stem cells able to mediate cross-tissue plasticity in mature intestines.Entities:
Keywords: SATB2, intestine regeneration, colonic mucosa, stem cell conversion, enhancer remodelingintestine
Mesh:
Year: 2021 PMID: 34582804 PMCID: PMC8741647 DOI: 10.1016/j.stem.2021.09.004
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 25.269