| Literature DB >> 29429899 |
Sara H Rouhanifard1, Aime Lopez Aguilar2, Lu Meng3, Kelley W Moremen3, Peng Wu4.
Abstract
At the base of the intestinal crypt, long-lived Lgr5+ stem cells are intercalated by Paneth cells that provide essential niche signals for stem cell maintenance. This unique epithelial anatomy makes the intestinal crypt one of the most accessible models for the study of adult stem cell biology. The glycosylation patterns of this compartment are poorly characterized, and the impact of glycans on stem cell differentiation remains largely unexplored. We find that Paneth cells, but not Lgr5+ stem cells, express abundant terminal N-acetyllactosamine (LacNAc). Employing an enzymatic method to edit glycans in cultured crypt organoids, we assess the functional role of LacNAc in the intestinal crypt. We discover that blocking access to LacNAc on Paneth cells leads to hyperproliferation of the neighboring Lgr5+ stem cells, which is accompanied by the downregulation of genes that are known as negative regulators of proliferation.Entities:
Keywords: LacNAc; Paneth cells; enteroid; enzymatic glycan engineering; glycosylation; intestinal stem cell
Mesh:
Substances:
Year: 2018 PMID: 29429899 PMCID: PMC5910180 DOI: 10.1016/j.chembiol.2018.01.010
Source DB: PubMed Journal: Cell Chem Biol ISSN: 2451-9448 Impact factor: 8.116