Prox1-positive cells monitor and sustain the murine intestinal epithelial cholinergic niche
Year: 2020
Type: article
Abstract: The enteric neurotransmitter acetylcholine governs important intestinal epithelial secretory and immune functions through its actions on epithelial muscarinic Gq-coupled receptors such as M3R. Its role in the regulation of intestinal stem cell function and differentiation, however, has not been clarified. Here, we find that nonselective muscarinic receptor antagonism in mice as well as epithelial-specific ablation of M3R induces a selective expansion of DCLK1-positive tuft cells, suggesting a model of feedback inhibition. Cholinergic blockade reduces Lgr5-positive intestinal stem cell tracing and cell number. In contrast, Prox1-positive endocrine cells appear as primary sensors of cholinergic blockade inducing the expansion of tuft cells, which adopt an enteroendocrine phenotype and contribute to increased mucosal levels of acetylcholine. This compensatory mechanism is lost with acute irradiation injury, resulting in a paucity of tuft cells and acetylcholine production. Thus, enteroendocrine tuft cells appear essential to maintain epithelial homeostasis following modifications of the cholinergic intestinal niche.
Source: Nature Communications
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $5,380
Awards: Limited Competition for the Continuation of the Intestinal Stem Cell Consortium Coordinating Center, The effects of Dysbiosis on intestinal stem cells, inflammation, and cancer, G1801228747, G189118987, Regulatory mechanism of gastric differentiation from gastric stem cells, G4389420412, Understanding stem cell heterogeneity and niche function in intestinal regeneration after irradiation, The role of stem cells and the microenvironment in gastrointestinal cancers
OpenAlex ID: W3000625295
