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在直肠乙状结肠型先天性巨结肠症和全结肠无神经节细胞症中,Cajal间质细胞数量减少。

Interstitial cells of Cajal reduce in number in recto-sigmoid Hirschsprung's disease and total colonic aganglionosis.

作者信息

Wang Hefeng, Zhang Yuhua, Liu Wei, Wu Rongde, Chen Xinguo, Gu Linuan, Wei Bin, Gao Yingmao

机构信息

Department of Pediatric Surgery, Shandong Provincial Hospital of Shandong University, Jinan, Shandong Province, China.

出版信息

Neurosci Lett. 2009 Feb 27;451(3):208-11. doi: 10.1016/j.neulet.2009.01.015. Epub 2009 Jan 13.

Abstract

Interstitial cells of Cajal (ICCs) play a key role in regulating gastrointestinal tract motility. The pathophysiological basis of colonic aperistalsis in Hirschsprung's disease (HD) is still not fully understood. Many studies reported that decreased numbers or disrupted networks of ICCs were associated with HD. Little information is available on the distribution of different subtypes of ICCs in HD. The aim of this study was to determine the alterations in density of different subtypes of ICC in colonic specimens of patients with total colonic and recto-sigmoid HD. Full thickness colonic specimens were obtained from five children with total colonic aganglionosis (TCA), sixteen with recto-sigmoid HD and seven controls. ICCs were visualized in frozen sections by c-Kit (CD117) fluorescent staining. In the control colon, c-Kit positive ICCs formed a dense network surrounding the myenteric plexus (IC-MY), along the submucosal surface of the circular muscle layer (IC-SM) and in the circular and longitudinal muscle layer (IC-IM). In the aganglionic region of the colon of the patients affected by HD, the number of ICCs (especially IC-IM and IC-SM) was markedly reduced and IC-MY networks were disrupted. Nearly total lack of three subtypes of ICCs was observed in the TCA specimens. This study demonstrated the altered distribution of different subtypes of ICCs in the resected colon of patients with recto-sigmoid HD and TCA. These findings suggest that the reduction of each subtype of ICCs may play an important role in the etiology of HD.

摘要

Cajal间质细胞(ICCs)在调节胃肠道蠕动中起关键作用。先天性巨结肠病(HD)中结肠无蠕动的病理生理基础仍未完全阐明。许多研究报道,ICCs数量减少或网络破坏与HD有关。关于HD中不同亚型ICCs的分布情况,目前所知甚少。本研究的目的是确定全结肠型和直肠乙状结肠型HD患者结肠标本中不同亚型ICCs密度的变化。从5例全结肠无神经节细胞症(TCA)患儿、16例直肠乙状结肠型HD患儿及7例对照者获取全层结肠标本。通过c-Kit(CD117)荧光染色在冰冻切片中观察ICCs。在对照结肠中,c-Kit阳性ICCs在肌间神经丛周围(IC-MY)、沿环肌层黏膜下表面(IC-SM)以及在环肌层和纵肌层(IC-IM)形成致密网络。在HD患者结肠的无神经节区域,ICCs数量(尤其是IC-IM和IC-SM)显著减少,IC-MY网络破坏。在TCA标本中几乎完全观察不到三种亚型的ICCs。本研究证实了直肠乙状结肠型HD和TCA患者切除结肠中不同亚型ICCs的分布改变。这些发现提示,各亚型ICCs的减少可能在HD的病因学中起重要作用。

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