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西格玛配体SR 31747A增强内毒素诱导的白细胞介素-10生成

Enhancement of endotoxin-induced interleukin-10 production by SR 31747A, a sigma ligand.

作者信息

Bourrie B, Bouaboula M, Benoit J M, Derocq J M, Esclangon M, Le Fur G, Casellas P

机构信息

Sanofi Recherche, Department of Immunopharmacology, Montpellier, France.

出版信息

Eur J Immunol. 1995 Oct;25(10):2882-7. doi: 10.1002/eji.1830251026.

Abstract

SR 31747A is a new sigma ligand eliciting immunosuppressive and anti-inflammatory properties. Here, we show that SR 31747A greatly enhances lipopolysaccharide (LPS)-induced systemic release of interleukin (IL)-10, while it inhibits the secretion of tumor necrosis factor (TNF)-alpha and interferon (IFN)-gamma. In line with this finding, we also show by using quantitative reverse transcription-polymerase chain reaction analysis that SR 31747A increased LPS-induced IL-10 mRNA accumulation in spleen cells, whereas the level of both TNF-alpha and IFN-gamma mRNA was dramatically decreased. The enhancement of IL-10 production by SR 31747A treatment was also apparent in nude and severe-combined immunodeficient mice treated with LPS, clearly indicating that T and B cells were not involved. Finally, SR 31747A conferred protection against the lethal effect of LPS. The finding that SR 31747A strongly stimulates the synthesis of the natural anti-inflammatory cytokine IL-10, a property not observed with dexamethasone, provides new insights for the clinical use of this original compound, particularly in chronic inflammatory diseases where IL-10 is believed to be a pivotal regulatory component.

摘要

SR 31747A是一种具有免疫抑制和抗炎特性的新型西格玛配体。在此,我们表明SR 31747A能极大地增强脂多糖(LPS)诱导的白细胞介素(IL)-10的全身释放,同时抑制肿瘤坏死因子(TNF)-α和干扰素(IFN)-γ的分泌。与此发现一致,我们还通过定量逆转录-聚合酶链反应分析表明,SR 31747A增加了LPS诱导的脾细胞中IL-10 mRNA的积累,而TNF-α和IFN-γ mRNA的水平则显著降低。在用LPS处理的裸鼠和严重联合免疫缺陷小鼠中,SR 31747A处理增强IL-10产生的现象也很明显,这清楚地表明T细胞和B细胞未参与其中。最后,SR 31747A对LPS的致死作用具有保护作用。SR 31747A强烈刺激天然抗炎细胞因子IL-10的合成,这一特性在地塞米松中未观察到,这为这种原始化合物的临床应用提供了新的见解,特别是在IL-10被认为是关键调节成分的慢性炎症性疾病中。

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