Division of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
Sci Rep. 2017 Jul 10;7(1):4950. doi: 10.1038/s41598-017-05064-y.
Psychological stress has been associated with intestinal epithelial hyperpermeability, the basic process in various functional and organic bowel diseases. In the present study, we aimed to clarify the differences and underlining mechanisms in stress-induced barrier disruption in functionally and structurally distinct epitheliums, including the villus epithelium (VE) and follicle-associated epithelium (FAE), a specialized epithelium overlaid the domes of Peyer's lymphoid follicles. Employing an Ussing Chamber system, the epithelial permeability was assessed in rats following water avoidance stress (WAS) in vivo and in mucosa tissues exposed to corticotropin-releasing factor (CRF) ex vivo. Decreased transepithelial resistance (TER) and increased paracellular and transcellular macromolecular permeability in colon, ileal VE and FAE had been observed in WAS rats and in CRF-exposed mucosa. Especially, the barrier dysfunction was more serious in the FAE. Moreover, WAS upregulated the expression of mast cell tryptase and protease-activated receptor-2 (PAR2), which positively correlated with epithelial conductance. Mast cell stabilizer cromolyn sodium obviously alleviated the barrier disruption induced by WAS in vivo and CRF in vitro. Serine protease inhibitor aprotinin and FUT-175, and selective PAR2 antagonist ENMD-1068 effectively inhibited the CRF-induced FAE hyperpermeability. Altogether, it concluded that the FAE was more susceptible to stress, and the mast cells and PAR2 signaling played crucial roles in this process.
心理应激与肠上皮通透性增加有关,而后者是多种功能性和器质性肠道疾病的基本过程。在本研究中,我们旨在阐明功能性和结构性不同的上皮细胞(包括绒毛上皮细胞(VE)和滤泡相关上皮细胞(FAE))中应激诱导的屏障破坏的差异及其潜在机制,FAE 是覆盖派氏淋巴滤泡顶部的一种特殊上皮细胞。采用 Ussing 室系统,在体内水回避应激(WAS)后和离体暴露于促肾上腺皮质释放因子(CRF)的黏膜组织中评估大鼠的上皮通透性。在 WAS 大鼠和 CRF 暴露的黏膜中,观察到结肠、回肠 VE 和 FAE 的跨上皮电阻(TER)降低,以及细胞旁和细胞内大分子通透性增加。特别是 FAE 的屏障功能障碍更为严重。此外,WAS 上调了肥大细胞胰蛋白酶和蛋白酶激活受体-2(PAR2)的表达,这与上皮电导呈正相关。肥大细胞稳定剂色甘酸钠明显减轻了体内 WAS 和体外 CRF 诱导的屏障破坏。丝氨酸蛋白酶抑制剂抑肽酶和 FUT-175 以及选择性 PAR2 拮抗剂 ENMD-1068 可有效抑制 CRF 诱导的 FAE 通透性增加。总之,结果表明 FAE 对应激更敏感,肥大细胞和 PAR2 信号通路在这一过程中起关键作用。