COMPOUNDS THAT INDUCE AUTOIMMUNITY IN THE BROWN-NORWAY RAT SENSITIZE MAST-CELLS FOR MEDIATOR RELEASE AND INTERLEUKIN-4 EXPRESSION

被引:69
作者
OLIVEIRA, DBG [1 ]
GILLESPIE, K [1 ]
WOLFREYS, K [1 ]
MATHIESON, PW [1 ]
QASIM, F [1 ]
COLEMAN, JW [1 ]
机构
[1] UNIV LIVERPOOL,DEPT PHARMACOL & THERAPEUT,LIVERPOOL L69 3BX,MERSEYSIDE,ENGLAND
关键词
MAST CELL; RAT; AUTOIMMUNITY; INTERLEUKIN-4;
D O I
10.1002/eji.1830250822
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 Th 2 response in the BN rat model of chemical-induced autoimmunity.
引用
收藏
页码:2259 / 2264
页数:6
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