Berin M C, Kiliaan A J, Yang P C, Groot J A, Taminiau J A, Perdue M H
Intestinal Diseases Research Program, McMaster University, Hamilton, Ontario, Canada.
Gastroenterology. 1997 Sep;113(3):856-64. doi: 10.1016/s0016-5085(97)70180-x.
BACKGROUND & AIMS: Intestine from sensitized rats develops a rapid secretory response to luminal antigen challenge that depends on activation of subepithelial mast cells. The aim of this study was to determine the timing and route of the transepithelial protein antigen transport.
Rats were sensitized to horseradish peroxidase (HRP). After 10-14 days, jejunal segments were resected, mounted in Ussing chambers, and challenged with HRP on the luminal side.
Electron microscopy of tissue specimens fixed at 2 minutes (before mast cell activation) showed enhanced endocytic uptake of HRP in enterocytes of HRP-sensitized rats compared with ovalbumin-sensitized or saline-injected controls. At this time, HRP was distributed throughout epithelial cells and was already evident in the lamina propria. In contrast, HRP was restricted to the apical region of enterocytes in controls. At 30 minutes (after mast cell activation), in HRP-sensitized rats only, HRP was also located within tight junctions and the paracellular region between epithelial cells. Tissue conductance was increased in HRP-sensitized rats beginning 30 minutes after HRP addition and correlated with the overall flux of HRP across the tissue.
The results show that specific sensitization enhances the initial uptake and transcytosis of antigen across intestinal epithelium. Subsequent to activation of mast cells, antigen transport is further enhanced by penetration through the paracellular pathway.
致敏大鼠的肠道对肠腔抗原刺激会产生快速分泌反应,该反应依赖于上皮下肥大细胞的激活。本研究的目的是确定经上皮蛋白抗原转运的时间和途径。
将大鼠对辣根过氧化物酶(HRP)进行致敏。10 - 14天后,切除空肠段,安装在尤斯灌流小室中,并在肠腔侧用HRP进行刺激。
对固定于2分钟(肥大细胞激活前)的组织标本进行电子显微镜检查显示,与卵清蛋白致敏或注射生理盐水的对照组相比,HRP致敏大鼠的肠上皮细胞中HRP的内吞摄取增强。此时,HRP分布于整个上皮细胞,并且在固有层中已经很明显。相比之下,对照组中HRP局限于肠上皮细胞的顶端区域。在30分钟(肥大细胞激活后),仅在HRP致敏大鼠中,HRP也位于紧密连接和上皮细胞之间的细胞旁区域。在添加HRP后30分钟开始,HRP致敏大鼠的组织电导增加,并且与HRP跨组织的总通量相关。
结果表明,特异性致敏增强了抗原跨肠上皮的初始摄取和转胞吞作用。肥大细胞激活后,抗原通过细胞旁途径的渗透进一步增强了转运。