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血红素加氧酶-1在牛磺酸氯胺和牛磺酸溴胺对J774.2巨噬细胞中前列腺素E2生成的下调作用中的角色。

The role of heme oxygenase-1 in down regulation of PGE2 production by taurine chloramine and taurine bromamine in J774.2 macrophages.

作者信息

Olszanecki R, Kurnyta M, Biedroń R, Chorobik P, Bereta M, Marcinkiewicz J

机构信息

Chair of Pharmacology, Jagiellonian University Medical College, Kraków, Poland.

出版信息

Amino Acids. 2008 Aug;35(2):359-64. doi: 10.1007/s00726-007-0609-x. Epub 2007 Dec 21.

Abstract

Taurine chloramine (TauCl) and taurine bromamine (TauBr), products of myeloperoxidase halide system, exert anti-inflammatory properties. TauCl was demonstrated to inhibit the production of a variety of pro-inflammatory mediators including cyclooxygenase-2 (COX-2) dependent production of prostaglandin E(2) (PGE(2)). Recently we have demonstrated that both major leukocyte haloamines, TauCl and TauBr, induced expression of HO-1 in non-activated and LPS-activated J774.2 macrophages. In this study, we have shown that TauCl and TauBr, at non-cytotoxic concentrations, inhibited the production of (PGE(2)) without altering the expression of COX-2 protein, in LPS/IFN-gamma stimulated J774.2 cells. The inhibitory effect of TauCl and TauBr was reversed by chromium III mesoporhyrin (CrMP), an inhibitor of HO-1 activity. Our data suggest that HO-1 might participate in anti-inflammatory effects of TauCl/TauBr possibly by inhibition of COX-2 activity and decrease of PGE(2) production.

摘要

髓过氧化物酶卤化物系统的产物氯胺牛磺酸(TauCl)和溴胺牛磺酸(TauBr)具有抗炎特性。已证实TauCl可抑制多种促炎介质的产生,包括环氧合酶-2(COX-2)依赖性的前列腺素E2(PGE2)的产生。最近我们证明,两种主要的白细胞卤胺,即TauCl和TauBr,均可在未激活和LPS激活的J774.2巨噬细胞中诱导血红素加氧酶-1(HO-1)的表达。在本研究中,我们发现,在LPS/γ干扰素刺激的J774.2细胞中,非细胞毒性浓度的TauCl和TauBr可抑制PGE2的产生,而不改变COX-2蛋白的表达。HO-1活性抑制剂三价铬中卟啉(CrMP)可逆转TauCl和TauBr的抑制作用。我们的数据表明,HO-1可能通过抑制COX-2活性和减少PGE2产生参与TauCl/TauBr的抗炎作用。

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