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Protease activated receptor 4 status of mast cells in post infectious irritable bowel syndrome
Authors:Han W  Wang Z  Lu X  Guo C
Institution:1. Department of Gastroenterology, Qilu Hospital of Shandong University, Jinan, Shandong Province, China;2. Department of Otolaryngology, Second Hospital of Shandong University, Jinan, Shandong Province, China;3. Department of Pathology, Qilu Hospital of Shandong University, Jinan, Shandong Province, China
Abstract:Background Growing evidence suggests that protease activated receptors (PARs) are mediators of persistent neuropathic pain, but their possible function as mediators in patients with post infectious irritable bowel syndrome (PI-IBS) remains to be further explored. This article aims to investigate the expression of PAR(2) and PAR(4) in the colonic mucosa of patients with PI-IBS, focusing on correlation with mast cell activation status. Methods A total of 17 normal controls and 23 patients with PI-IBS volunteered the study. The expression and localization of PAR(2) and PAR(4) were investigated by RT-PCR and immunohistochemistry, and the expression of PAR(2) and PAR(4) in the mast cells was examined using double-immunofluorescence staining. Key Results The immunohistochemical study revealed that epithelial and submucosal cells showed immunoreactivity for both PAR(2) and PAR(4) . Protease activated receptor 4 mRNA expression and immunoreactivity were down-regulated in PI-IBS compared with the control group. Specifically, a reduced immunoreactivity for PAR(4) was observed in mast cells of PI-IBS compared with normal controls, whereas there are no significant differences shown in PAR(2) between the PI-IBS and the control group. It is also found that the PAR(4) immunoreactivity decreases, while the activity of mast cells increases in PI-IBS rather than normal controls. Conclusions & Inferences This study outlines the down-regulation of PAR(4) in the mast cells of PI-IBS. It could be of considerable interests in understanding the mechanisms involved in the persistent colonic hypersensitivity and their potential role as therapeutic targets for PI-IBS.
Keywords:inflammation  irritable bowel syndrome  mast cells  protease activated receptors
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