Cathelicidin regulates goblet cell mucus secretion and mucus-associated proteins in <i>Citrobacter rodentium</i>-induced colitis.

Abstract

Colonic goblet cells play a crucial role in mucosal defense by secreting Muc2 mucin and other proteins that entrap and expel enteropathogens. However, the role of innate effectors in the gut like cathelicidin peptides in regulating the mucus barrier during infections remains unclear. In this study, we used cathelicidin-deficient (<i>Camp</i>^<i>-/-</i>) littermates, colonoids, and human LS174T goblet-like cells to investigate how cathelicidin modulates goblet cell function and mucosal defense against attaching/effacing enteropathogen <i>Citrobacter rodentium</i>. We showed that increased fecal shedding and epithelial colonization by <i>C. rodentium</i> in <i>Camp</i>^<i>-/-</i> littermates was accompanied by impaired mucus secretion and higher retention of mucin granules and trefoil factor 3 (Tff3) in bloated colonic goblet cells. Reduction in mucus secretion by goblet cells was accompanied by reduced reactive oxygen species (ROS) production during <i>C. rodentium</i> infection in <i>Camp</i>^<i>-/-</i> as compared to <i>Camp</i>^<i>+/+</i> littermate controls. In LS174T goblet-like cells, human cathelicidin LL-37 stimulated the secretion of TFF3 and resistin-like molecule β (RELMβ) in a ROS-dependent manner. These findings reveal that cathelicidin regulates goblet cell mucus and mucus-associated protein secretion through a ROS-mediated mechanism critical for bacterial clearance and maintenance of gut homeostasis.