Epithelial genetic muscarinic receptor 3 ablation induces sex-specific modulation of colonic intestinal progenitor cells and response to intestinal injury

Abstract Background & Aims Epithelial muscarinic acetylcholine receptor subtype 3 (M3R) signaling modulates intestinal stem and progenitor cell function, yet its impact on colonic homeostasis remains unclear. Hence, this study explores the sex-specific effects of epithelial genetic M3R ablation...

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Vydáno v:Journal of Crohn's and colitis Ročník 19; číslo 6
Hlavní autoři: Ragab, Mohab, Wieland, Jessica, Waldherr Avila de Melo, Caroline, Agibalova, Tatiana, Ermolova, Anastasia, Durner, Niklas, Hempel, Anneke, Heindl, Fabian, Maurer, H Carlo, Steiger, Katja, Janssen, Klaus-Peter, Tschurtschenthaler, Markus, Wang, Timothy C, Quante, Michael, Schmid, Roland M, Middelhoff, Moritz
Médium: Journal Article
Jazyk:angličtina
Vydáno: UK Oxford University Press 04.06.2025
Témata:
Animals
Colitis - genetics
Colitis - metabolism
Colitis - pathology
Colon - cytology
Colon - metabolism
Colon - pathology
Disease Models, Animal
Female
Humans
Intestinal Mucosa - cytology
Intestinal Mucosa - metabolism
Intestinal Mucosa - pathology
Male
Mice
Muscarinic Agonists - pharmacology
Receptor, Muscarinic M3 - genetics
Receptor, Muscarinic M3 - metabolism
Receptors, G-Protein-Coupled - metabolism
Sex Factors
Stem Cells - metabolism
epithelial muscarinic receptor 3
colonic progenitor cells
colitis
ISSN:1873-9946, 1876-4479, 1876-4479
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Shrnutí:Abstract Background & Aims Epithelial muscarinic acetylcholine receptor subtype 3 (M3R) signaling modulates intestinal stem and progenitor cell function, yet its impact on colonic homeostasis remains unclear. Hence, this study explores the sex-specific effects of epithelial genetic M3R ablation and muscarinic receptor agonism on murine colonic Lgr5-EGFP+ progenitor cells and epithelial homeostasis. Methods Genetic ablation of M3R was achieved using Vil-Cre × M3R fl/fl mice. The effects on Lgr5-expressing progenitor cells, epithelial homeostasis, and response to intestinal injury were assessed, with attention to sex-specific differences. Effects of cholinergic and muscarinic agonism on epithelial cell homeostasis were evaluated employing murine and human colonoids. Results Genetic epithelial ablation of the M3R employing Vil-Cre × M3R fl/fl mice interestingly resulted in the prominent reduction in Lgr5-expressing progenitor cells in male tissues, contrasting an expansion of Lgr5-expressing cells in female colonic epithelia. This difference was abrogated in young female Vil-Cre × M3R fl/fl mice, which harbor reduced circulating sex hormone levels. Genetic M3R ablation further induced changes to epithelial differentiation. Importantly, male Vil-Cre × M3R fl/fl mice developed severe inflammation following induction of acute experimental colitis, which did almost not affect female Vil-Cre × M3R fl/fl mice. Moreover, sex-specific effects of modulations of cholinergic and muscarinic signaling on epithelial cells could be corroborated in murine and human colonoids. Conclusions Our data reveal sex differences in the modulation of intestinal, colonic epithelial cells by cholinergic, muscarinic signaling and highlight the potential for therapeutic strategies targeting cholinergic receptor signaling in colonic inflammatory diseases. Graphical Abstract Graphical Abstract
Bibliografie:ObjectType-Article-1
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content type line 23
ISSN:1873-9946
1876-4479
1876-4479
DOI:10.1093/ecco-jcc/jjaf038