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肥大细胞对大鼠肠道跨上皮抗原转运途径的影响。

The influence of mast cells on pathways of transepithelial antigen transport in rat intestine.

作者信息

Berin M C, Kiliaan A J, Yang P C, Groot J A, Kitamura Y, Perdue M H

机构信息

Intestinal Disease Research Program, McMaster University, Hamilton, Canada.

出版信息

J Immunol. 1998 Sep 1;161(5):2561-6.

PMID:9725256
Abstract

Luminal Ag challenge of intestinal segments from sensitized rats results in a rapid (approximately 3 min) secretory response. We previously showed in horseradish peroxidase (HRP)-sensitized rats that the initial phase of transepithelial Ag transport occurred via a transcellular route and was enhanced by sensitization. However, following the hypersensitivity reaction, Ag also crossed between epithelial cells. The aim of this study was to determine the role of mast cells in the altered transepithelial Ag transport. White spotting mast cell-deficient rats and +/+ littermate controls were sensitized to HRP. After 10 to 14 days, jejunal segments were resected, mounted in Ussing chambers, and challenged with HRP on the luminal side. Electron microscopy of jejunum fixed at 2 min showed a similarly enhanced endocytic transport of HRP in sensitized +/+ and Ws/Ws rats compared with naive controls. In sensitized +/+ rats, a secretory response occurred approximately 3 min after challenge, and tissue conductance increased thereafter. Naive +/+ and sensitized Ws/Ws rats did not demonstrate a secretory response to HRP challenge, and conductance remained at baseline levels. The flux of HRP was elevated across tissue from sensitized +/+ rats but not across tissue from naive controls or sensitized Ws/Ws rats. The results indicate that sensitization enhances the initial phase of transepithelial uptake of Ag by transcytosis in a mast cell-independent manner. However, subsequent recruitment of the paracellular pathway for Ag transport in sensitized rats is dependent upon the presence of mast cells and occurs after the activation of such cells.

摘要

对致敏大鼠的肠段进行腔内抗原刺激会引发快速(约3分钟)的分泌反应。我们之前在辣根过氧化物酶(HRP)致敏的大鼠中发现,跨上皮抗原转运的初始阶段是通过跨细胞途径进行的,并且致敏会增强这种转运。然而,在过敏反应之后,抗原也会在上皮细胞之间穿过。本研究的目的是确定肥大细胞在改变的跨上皮抗原转运中的作用。将白色斑点肥大细胞缺陷型大鼠及其同窝对照(+/+)致敏于HRP。10至14天后,切除空肠段,安装在尤斯灌流小室中,并在腔侧用HRP进行刺激。对2分钟时固定的空肠进行电子显微镜检查显示,与未致敏对照相比,致敏的+/+和Ws/Ws大鼠中HRP的内吞转运同样增强。在致敏的+/+大鼠中,刺激后约3分钟出现分泌反应,此后组织电导增加。未致敏的+/+和致敏的Ws/Ws大鼠对HRP刺激未表现出分泌反应,电导保持在基线水平。HRP从致敏的+/+大鼠的组织中通量升高,但从未致敏对照或致敏的Ws/Ws大鼠的组织中通量未升高。结果表明,致敏以肥大细胞非依赖的方式通过转胞吞作用增强了跨上皮摄取抗原的初始阶段。然而,致敏大鼠中随后招募的抗原转运旁细胞途径依赖于肥大细胞的存在,并且在这些细胞激活后发生。

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