Critical role of thrombospondin-1 in promoting intestinal mucosal wound repair

• Published in: JCI insight Vol. 9; no. 17
• Main Authors: Wilson, Zachary S, Raya-Sandino, Arturo, Miranda, Jael, Fan, Shuling, Brazil, Jennifer C, Quiros, Miguel, Garcia-Hernandez, Vicky, Liu, Qingyang, Kim, Chang H, Hankenson, Kurt D, Nusrat, Asma, Parkos, Charles A
• Format: Journal Article
• Language: English
• Published: United States American Society for Clinical Investigation 30.07.2024
• Subjects: Animals; CD47 Antigen - genetics; CD47 Antigen - metabolism; Cell Movement; Colon - metabolism; Colon - pathology; Epithelial Cells - metabolism; Humans; Intestinal Mucosa - metabolism; Intestinal Mucosa - pathology; Male; Mice; Mice, Knockout; Neuropeptides; rac1 GTP-Binding Protein - metabolism; rhoA GTP-Binding Protein - metabolism; Thrombospondin 1 - genetics; Thrombospondin 1 - metabolism; Transforming Growth Factor beta1 - metabolism; Wound Healing - physiology; Inflammatory bowel disease; Cytoskeleton; Inflammation; Cell migration/adhesion; Gastroenterology
• ISSN: 2379-3708; 2379-3708
• DOI: 10.1172/jci.insight.180608

Thrombospondin-1 (TSP1) is a matricellular protein associated with the regulation of cell migration through direct binding interactions with integrin proteins and by associating with other receptors known to regulate integrin function, including CD47 and CD36. We previously demonstrated that deletion of an epithelial TSP1 receptor, CD47, attenuates epithelial wound repair following intestinal mucosal injury. However, the mechanisms by which TSP1 contributes to intestinal mucosal repair remain poorly understood. Our results show upregulated TSP1 expression in colonic mucosal wounds and impaired intestinal mucosal wound healing in vivo upon intestinal epithelium-specific loss of TSP1 (VillinCre/+ Thbs1fl/fl or Thbs1ΔIEC mice). We report that exposure to exogenous TSP1 enhanced migration of intestinal epithelial cells in a CD47- and TGF-β1-dependent manner and that deficiency of TSP1 in primary murine colonic epithelial cells resulted in impaired wound healing. Mechanistically, TSP1 modulated epithelial actin cytoskeletal dynamics through suppression of RhoA activity, activation of Rho family small GTPase (Rac1), and changes in filamentous-actin bundling. Overall, TSP1 was found to regulate intestinal mucosal wound healing via CD47 and TGF-β1, coordinate integrin-containing cell-matrix adhesion dynamics, and remodel the actin cytoskeleton in migrating epithelial cells to enhance cell motility and promote wound repair.