Gfroerer Stefan, Rolle Udo
Department of Paediatric Surgery, University Hospital, Goethe University Frankfurt/M, 60596 Frankfurt/M, Germany,
Pediatr Surg Int. 2013 Sep;29(9):889-97. doi: 10.1007/s00383-013-3364-y.
Hirschsprung disease (HD) is the most prevalent congenital gastrointestinal motility disorder. The pathogenesis of HD is defined as a functional intestinal obstruction resulting from a defect in the intrinsic innervation of the distal bowel. In addition to the enteric nervous system, the interstitial cells of Cajal (ICC) play an important role in the generation of coordinated gastrointestinal peristalsis. The major function of the ICCs is the generation of slow waves that allow these cells to act as specialised pacemaker cells within various tissues. ICCs have additional functions in the gastrointestinal tract as regulators of mechanical activity and neurotransmission. Due to the central role of ICCs in gastrointestinal peristalsis, it has been suggested that defects or impairments of the ICCs may contribute to motility dysfunction in several gastrointestinal motility disorders. This review describes the distribution and functions of ICCs in the normal gut and in Hirschsprung disease.
先天性巨结肠症(HD)是最常见的先天性胃肠动力障碍疾病。HD的发病机制被定义为远端肠道固有神经支配缺陷导致的功能性肠梗阻。除了肠神经系统外, Cajal间质细胞(ICC)在协调胃肠蠕动的产生中也起着重要作用。 ICC的主要功能是产生慢波,使这些细胞能够作为各种组织中的特殊起搏细胞发挥作用。 ICC在胃肠道中还具有作为机械活动和神经传递调节因子的额外功能。由于ICC在胃肠蠕动中起着核心作用,因此有人提出,ICC的缺陷或损伤可能导致几种胃肠动力障碍中的动力功能障碍。这篇综述描述了ICC在正常肠道和先天性巨结肠症中的分布和功能。