Interstitial cells of cajal in reflux esophagitis: role in the pathogenesis of the disease

被引:1
|
作者
Shafik, A
Ahmed, I
El Sibai, O
Shafik, AA
机构
[1] Cairo Univ, Fac Med, Dept Surg & Expt Res, Cairo, Egypt
[2] Menoufia Univ, Dept Surg, Fac Med, Shibin Al Kawm, Egypt
来源
MEDICAL SCIENCE MONITOR | 2005年 / 11卷 / 12期
关键词
gastroesophageal reflux; esophagogastric junction; c-kit; esophagogastric junction incompetence; slow waves; action potentials;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Interstitial cells of Cajal (ICCs) are claimed to be involved in gut electromotor activity. We investigated whether absent or diminished ICCs in the esophagogastri c junction (EGJ) may be responsible for EGJ incompetence in gastro-esophageal reflux disease (GERD). Material/ Methods: Endoscopic specimens were obtained from the upper and mid third of the esophagus and from the EGJ of 29 patients (17 men, 12 women, mean age: 46.7 years) with GERD (5 grade A, 5 B, 6 C, and 13 D, Los Angeles classification) and from 8 controls. Sections were prepared for immmohistochemical investigation using an ICC marker c-kit. Controls had normal rabbit serum substituted for the primary antiserum. Results: C-kit-positive branched ICC-like cells were detected in the esophageal and EGJ musculature of the controls. They were distinguishable from the c-kit-negative unbranched smooth muscle cells and from the c-kit-positive unbranched mast cells. Immunoreactivity was absent in the negative controls. ICCs in the esophageal body existed in GERD and in controls, but were absent from the EGJ of 12 patients (2 grade C, 10 D) and occasionally detected in 5 of group A, 5 of B, 4 of C, and 3 of group D patients. Conclusions: ICCs were demonstrated in the esophageal body and EGJ of controls. In GERD patients they were detected in the esophageal body, but were deficient or absent in the EGJ. It is postulated that ICC absence or deficiency is responsible for EGJ incompetence and GER. The cause of ICC deficiency or absence needs to be investigated.
引用
收藏
页码:BR452 / BR456
页数:5
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