Cdc42 Coordinates Proliferation, Polarity, Migration, and Differentiation of Small Intestinal Epithelial Cells in Mice
| Autor: | Yi Zheng, Shailaja Akunuru, Jaime Melendez, Ming Liu, Leesa Sampson, David P. Witte, Jefferson E. Vallance, Noah F. Shroyer, Xiaonan Han |
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| Rok vydání: | 2013 |
| Předmět: |
Cellular differentiation
macromolecular substances Biology digestive system Article Mice Intestinal mucosa Cell Movement Intestine Small Cell polarity medicine Animals Intestinal Mucosa Progenitor cell cdc42 GTP-Binding Protein Cell Proliferation Intestinal permeability Hepatology Gastroenterology Cell Polarity Cell Differentiation medicine.disease Intestinal epithelium Microvillus Cell biology medicine.anatomical_structure Cdc42 GTP-Binding Protein |
| Zdroj: | Gastroenterology. 145:808-819 |
| ISSN: | 0016-5085 |
| Popis: | Background & Aims Cdc42 is a Rho GTPase that regulates diverse cellular functions, including proliferation, differentiation, migration, and polarity. In the intestinal epithelium, a balance among these events maintains homeostasis. We used genetic techniques to investigate the role of Cdc42 in intestinal homeostasis and its mechanisms. Methods We disrupted Cdc42 specifically in intestinal epithelial cells by creating Cdc42flox/flox-villin-Cre+ and Cdc42flox/flox-Rosa26-CreER+ mice. We collected intestinal and other tissues, and analyzed their cellular, molecular, morphologic, and physiologic features, compared with the respective heterozygous mice. Results In all mutant mice studied, the intestinal epithelium had gross hyperplasia, crypt enlargement, microvilli inclusion, and abnormal epithelial permeability. Cdc42 deficiency resulted in defective Paneth cell differentiation and localization without affecting the differentiation of other cell lineages. In mutant intestinal crypts, proliferating stem and progenitor cells increased, compared with control mice, resulting in increased crypt depth. Cdc42 deficiency increased migration of stem and progenitor cells along the villi, caused a mild defect in the apical junction orientation, and impaired intestinal epithelium polarity, which can contribute to the observed defective intestinal permeability. The intestinal epithelium of the Cdc42flox/flox-villin-Cre+ and Cdc42flox/flox-Rosa26-CreER+ mice appeared similar to that of patients with microvillus inclusion disease. In the digestive track, loss of Cdc42 also resulted in crypt hyperplasia in the colon, but not the stomach. Conclusions Cdc42 regulates proliferation, polarity, migration, and differentiation of intestinal epithelial cells in mice and maintains intestine epithelial barrier and homeostasis. Defects in Cdc42 signaling could be associated with microvillus inclusion disease. |
| Databáze: | OpenAIRE |
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