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在棕色挪威大鼠中诱导自身免疫的化合物使肥大细胞对介质释放和白细胞介素-4表达敏感。

Compounds that induce autoimmunity in the brown Norway rat sensitize mast cells for mediator release and interleukin-4 expression.

作者信息

Oliveira D B, Gillespie K, Wolfreys K, Mathieson P W, Qasim F, Coleman J W

机构信息

Department of Medicine, University of Cambridge School of Clinical Medicine, Addenbrooke's Hospital, GB.

出版信息

Eur J Immunol. 1995 Aug;25(8):2259-64. doi: 10.1002/eji.1830250822.

Abstract

Brown Norway (BN) rats given mercuric chloride (HgCl2), gold (Au) salts or D-penicillamine develop a T helper 2 (Th2) cell-mediated autoimmune syndrome. The recent observation of tissue injury within 24 h of HgCl2 treatment suggested the involvement of a non-T cell. We therefore examined the effect of these compounds on rat mast cells in vitro. Incubation of BN rat peritoneal mast cells with HgCl2 enhanced the release of serotonin in response to IgE cross-linking agents. Mast cells from Lewis rats, a strain not susceptible to the autoimmune syndrome in vivo, were affected to a lesser extent. The effect was observed with purified BN mast cells, suggesting a direct action. Similar effects were seen with D-penicillamine in the presence of copper ions, a combination that produces hydrogen peroxide, and Au. HgCl2 caused significant induction of interleukin (IL)-4 mRNA in mast cells from BN, but not Lewis rats. The data demonstrate a novel enhancing effect of a number of compounds on mast cell mediator release, and an inducing effect of HgCl2 on mast cell IL-4, expression. These findings are consistent with our hypotheses that mast cells may contribute to early tissue injury, and also, via production of IL-4, may initiate and/or augment, the Th2 response in the BN rat model of chemical-induced autoimmunity.

摘要

给棕色挪威(BN)大鼠注射氯化汞(HgCl2)、金(Au)盐或D-青霉胺会引发辅助性T细胞2(Th2)细胞介导的自身免疫综合征。最近观察到在HgCl2处理后24小时内出现组织损伤,提示有非T细胞参与。因此,我们在体外研究了这些化合物对大鼠肥大细胞的影响。用HgCl2孵育BN大鼠腹膜肥大细胞可增强其对IgE交联剂的反应中5-羟色胺的释放。来自Lewis大鼠(一种在体内不易患自身免疫综合征的品系)的肥大细胞受影响程度较小。在纯化的BN肥大细胞中观察到这种效应,表明是直接作用。在存在产生过氧化氢的铜离子和Au的情况下,D-青霉胺也有类似作用。HgCl2可显著诱导BN大鼠而非Lewis大鼠肥大细胞中白细胞介素(IL)-4 mRNA的表达。数据表明多种化合物对肥大细胞介质释放有新的增强作用,以及HgCl2对肥大细胞IL-4表达有诱导作用。这些发现与我们的假设一致,即肥大细胞可能导致早期组织损伤,并且还可能通过产生IL-4在化学诱导自身免疫的BN大鼠模型中启动和/或增强Th2反应。

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