Department of Paediatric Surgery and Paediatric Urology, University Hospital Frankfurt, Goethe University Frankfurt, Theodor-Stern-Kai 7, 60590, Frankfurt, Germany.
Pediatr Surg Int. 2023 Apr 27;39(1):188. doi: 10.1007/s00383-023-05467-1.
Interstitial cells of Cajal (ICCs) are pacemaker cells of gastrointestinal motility that generate and transmit electrical slow waves to smooth muscle cells in the gut wall, thus inducing phasic contractions and coordinated peristalsis. Traditionally, tyrosine-protein kinase Kit (c-kit), also known as CD117 or mast/stem cell growth factor receptor, has been used as the primary marker of ICCs in pathology specimens. More recently, the Ca-activated chloride channel, anoctamin-1, has been introduced as a more specific marker of ICCs. Over the years, various gastrointestinal motility disorders have been described in infants and young children in which symptoms of functional bowel obstruction arise from ICC-related neuromuscular dysfunction of the colon and rectum. The current article provides a comprehensive overview of the embryonic origin, distribution, and functions of ICCs, while also illustrating the absence or deficiency of ICCs in pediatric patients with Hirschsprung disease intestinal neuronal dysplasia, isolated hypoganglionosis, internal anal sphincter achalasia, and congenital smooth muscle cell disorders such as megacystis microcolon intestinal hypoperistalsis syndrome.
Cajal 间质细胞(ICCs)是胃肠道运动的起搏细胞,它们产生并向肠壁平滑肌细胞传递电慢波,从而诱导相性收缩和协调蠕动。传统上,酪氨酸蛋白激酶 Kit(c-kit),也称为 CD117 或肥大/干细胞生长因子受体,被用作病理标本中 ICCs 的主要标志物。最近,钙激活氯离子通道,anoctamin-1,被引入作为 ICCs 的更特异性标志物。多年来,在婴儿和幼儿中描述了各种胃肠道动力障碍,其中功能性肠梗阻的症状源于结肠和直肠与 ICC 相关的神经肌肉功能障碍。本文全面概述了 ICCs 的胚胎起源、分布和功能,同时还说明了在先天性巨结肠、肠神经元发育不良、孤立性低神经节细胞症、内括约肌失弛缓症和先天性平滑肌细胞疾病(如巨膀胱-微结肠-肠蠕动不良综合征)的儿科患者中 ICCs 的缺失或缺乏。