Department of Cellular and Molecular Medicine, Faculty of Health Sciences, University of Copenhagen, Copenhagen N, Denmark.
J Cell Mol Med. 2010 Apr;14(4):818-32. doi: 10.1111/j.1582-4934.2010.01025.x. Epub 2010 Jan 30.
Interstitial cells of Cajal (ICC) are recognized as pacemaker cells for gastrointestinal movement and are suggested to be mediators of neuromuscular transmission. Intestinal motility disturbances are often associated with a reduced number of ICC and/or ultrastructural damage, sometimes associated with immune cells. Macrophages and mast cells in the intestinal muscularis externa of rodents can be found in close spatial contact with ICC. Macrophages are a constant and regularly distributed cell population in the serosa and at the level of Auerbach's plexus (AP). In human colon, ICC are in close contact with macrophages at the level of AP, suggesting functional interaction. It has therefore been proposed that ICC and macrophages interact. Macrophages and mast cells are considered to play important roles in the innate immune defence by producing pro-inflammatory mediators during classical activation, which may in itself result in damage to the tissue. They also take part in alternative activation which is associated with anti-inflammatory mediators, tissue remodelling and homeostasis, cancer, helminth infections and immunophenotype switch. ICC become damaged under various circumstances - surgical resection, possibly post-operative ileus in rodents - where innate activation takes place, and in helminth infections - where alternative activation takes place. During alternative activation the muscularis macrophage can switch phenotype resulting in up-regulation of F4/80 and the mannose receptor. In more chronic conditions such as Crohn's disease and achalasia, ICC and mast cells develop close spatial contacts and piecemeal degranulation is possibly triggered.
Cajal 间质细胞(ICC)被认为是胃肠道运动的起搏细胞,并且被认为是神经肌肉传递的介质。肠道运动障碍通常与 ICC 的数量减少和/或超微结构损伤有关,有时与免疫细胞有关。啮齿动物肠外膜的巨噬细胞和肥大细胞可以与 ICC 紧密空间接触。巨噬细胞是在浆膜和 Auerbach 丛(AP)水平上恒定且均匀分布的细胞群。在人类结肠中,ICC 在 AP 水平与巨噬细胞密切接触,提示存在功能相互作用。因此,有人提出 ICC 和巨噬细胞相互作用。巨噬细胞和肥大细胞被认为通过在经典激活过程中产生促炎介质在先天免疫防御中发挥重要作用,这本身可能导致组织损伤。它们还参与替代激活,与抗炎介质、组织重塑和动态平衡、癌症、寄生虫感染和免疫表型转换有关。ICC 在各种情况下都会受损 - 手术切除,啮齿动物可能会发生术后肠梗阻 - 先天激活发生,在寄生虫感染中 - 替代激活发生。在替代激活期间,肌层巨噬细胞可以改变表型,导致 F4/80 和甘露糖受体的上调。在更慢性的疾病中,如克罗恩病和贲门失弛缓症,ICC 和肥大细胞会形成紧密的空间接触,可能会触发颗粒状脱粒。