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Journal of Molecular Endocrinology (2005) 35, 201-209    DOI: 10.1677/jme.1.01787
© 2005 Society for Endocrinology

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Differential expression of endothelin-2 along the mouse intestinal tract

Satoshi Takizawa1, Tsuyoshi Uchide2, Javier Adur1,3, Takaharu Kozakai1, Eiichi Kotake-Nara1,3, Jiexia Quan1 and Kaname Saida1,4

1 Institute for Biological Resources and Functions, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki 305-8566, Japan
2 Department of Toxicology, School of Veterinary Medicine and Animal Sciences, Kitasato University, Towada, Aomori 034-8628, Japan
3 New Energy and Industrial Technology Development Organization (NEDO), 16F, MUZA KAWASAKI Central Tower 1310 Omiya-cho, Saiwai-ku, Kawasaki, Kanagawa 212-8554, Japan
4 Human Stress Signal Research Center, National Institute of Advanced Industrial Science and Technology (AIST), Ikeda, Osaka 536-8577, Japan

(Requests for offprints should be addressed to K Saida; email: k.saida{at}aist.go.jp)

Endothelin (ET)-2, an ET family peptide, is highly expressed in intestine. However, the specific distribution and function of ET-2 remain unknown. We elucidated the expression profile and localization of ET-2 in mouse gastrointestinal tract. Real-time PCR analysis revealed that ET-2 gene expression in the gastrointestinal tract of healthy animals was relatively high in the colon. Immunohistochemical analysis revealed ET-2-like immunoreactivity mainly in epithelial cells of the mucosa throughout the intestinal tract of healthy animals. Intracellularly, ET-2 was concentrated close to the basement membrane of intestinal epithelial cells. A weak ET-2-like immunoreactivity was also localized to some neurofibers and the myenteric plexus of the muscle layer, coexpressing with vasoactive intestinal peptide. ET-2-like immunoreactivity was also detected at Brunner’s glands of the duodenum and follicle-associated epithelium of Peyer’s patch. In contrast, ET-1-like immunoreactivity was uniformly distributed in epithelial cells. In dextran sulfate sodium (DSS)-induced colitis, colonic ET-2 was upregulated during the late stage of DSS treatment. These results suggest that in intestinal epithelial cells ET-2 could be secreted into the lamina propria and the dome region in Peyer’s patch, and that it might modulate immune cells in these sites for mucosal defense.




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