首页> 美国卫生研究院文献>Journal of Cellular and Molecular Medicine >Interstitial cells of Cajal macrophages and mast cells in the gut musculature: morphology distribution spatial and possible functional interactions
【2h】

Interstitial cells of Cajal macrophages and mast cells in the gut musculature: morphology distribution spatial and possible functional interactions

机译:肠道肌肉中Cajal巨噬细胞和肥大细胞的间质细胞:形态分布空间和可能的功能相互作用

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

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.
机译:Cajal间质细胞(ICC)被认为是胃肠运动的起搏器细胞,并被认为是神经肌肉传递的介质。肠蠕动障碍通常与ICC和/或超微结构损伤数量减少有关,有时与免疫细胞有关。啮齿类动物肠道肌层外部的巨噬细胞和肥大细胞可与ICC紧密空间接触。巨噬细胞是浆膜和Auerbach丛(AP)水平上恒定且规则分布的细胞群。在人类结肠中,ICC在AP水平与巨噬细胞紧密接触,表明功能相互作用。因此,已经提出ICC和巨噬细胞相互作用。巨噬细胞和肥大细胞被认为在经典激活过程中通过产生促炎性介质而在先天免疫防御中起重要作用,这本身可能导致组织损伤。它们还参与与抗炎介质,组织重塑和体内平衡,癌症,蠕虫感染和免疫表型转换有关的替代激活。在各种情况下,ICC都会受到损坏-手术切除,可能是啮齿动物的肠梗阻-发生先天性激活,而在蠕虫感染中-发生其他激活。在替代性激活过程中,肌层巨噬细胞可以切换表型,从而导致F4 / 80和甘露糖受体的上调。在克罗恩病和门失弛缓症等慢性病中,ICC和肥大细胞会形成紧密的空间接触,并且可能触发零碎的脱粒。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号