Parkos C A
Department of Pathology and Laboratory Medicine, Emory University, Atlanta, Georgia 30322, USA.
Am J Physiol. 1997 Oct;273(4):G763-8. doi: 10.1152/ajpgi.1997.273.4.G763.
In many inflammatory conditions of the gastrointestinal tract, disease activity and patient symptoms correlate with the histological finding of neutrophil (PMN) migration across the epithelium. PMN interactions with intestinal epithelium can influence epithelial functions ranging from barrier maintenance to electrolyte secretion. Additionally, PMN recruitment to the epithelium can be modulated by epithelial interactions with luminal enteric pathogens. Adhesive interactions between PMN and intestinal epithelial cells have been shown to be distinct from interactions of PMN with endothelia. In particular, PMN transepithelial migration is modulated by a distinct array of cytokines including interferon-gamma and interleukin-4 and requires the PMN beta2-integrin CD11b/CD18 but is independent of CD11a/CD18, selectins, and intercellular adhesion molecule 1. Additionally, an integral membrane protein termed CD47 has recently been shown to play an important role in PMN transepithelial migration at point(s) subsequent to initial adhesive interactions. This article provides a brief overview of PMN interactions with epithelia and their functional consequences in relation to inflammatory disease.
在许多胃肠道炎症性疾病中,疾病活动度和患者症状与中性粒细胞(PMN)穿过上皮迁移的组织学表现相关。PMN与肠上皮的相互作用可影响从屏障维持到电解质分泌等多种上皮功能。此外,上皮与肠腔病原体的相互作用可调节PMN向上皮的募集。已表明PMN与肠上皮细胞之间的黏附相互作用不同于PMN与内皮细胞的相互作用。特别是,PMN跨上皮迁移受包括干扰素-γ和白细胞介素-4在内的一系列独特细胞因子调节,需要PMNβ2整合素CD11b/CD18,但独立于CD11a/CD18、选择素和细胞间黏附分子1。此外,一种名为CD47的整合膜蛋白最近已被证明在初始黏附相互作用后的某个时间点在PMN跨上皮迁移中起重要作用。本文简要概述了PMN与上皮的相互作用及其与炎症性疾病相关的功能后果。