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TREM-1 是 U937 泡沫细胞中 TNF-α 和 IL-8 产生的正调节剂。

TREM-1 is a positive regulator of TNF-α and IL-8 production in U937 foam cells.

机构信息

Department of Cardiovascular, First Hospital of Jilin University, 71 Xinmin of Chaoyang district, Changchun 130021, China.

出版信息

Bosn J Basic Med Sci. 2012 May;12(2):94-101. doi: 10.17305/bjbms.2012.2503.

Abstract

The purpose of our study was to investigate the expression levels of TREM-1 (triggering receptor expressed on myeloid cells-1) in U937 foam cells and determine whether TREM-1 regulates the production of tumor necrosis factor-alpha and interleukin-8 in these cells. Human U937 cells were incubated with phorbol 12-myristate 13-acetate and then oxidized human low-density lipoprotein to induce foam cell formation. Oil red O staining was used to identify the foam cells. The production of IL-8 and TNF-α by U937 foam cells was assayed by enzyme-linked immunosorbent assay. The expression of TREM-1 mRNA in U937 foam cells was detected by reverse transcription-polymerase chain reaction. Moreover, U937 foam cells were transfected by small interfering RNA using Lipofectamine 2000 to knockdown TREM-1. Western blot was performed to assay protein expression of TREM-1 and ELISA was used to examine the effect of TREM-1 knockdown on IL-8 and TNF-α production. PMA and ox-LDL induced U937 cells to form foam cells. The production of TNF-α and IL-8 was found to be significantly elevated in U937 foam cells, concomitant with a significant up-regulation of TREM-1 mRNA. TREM-1 siRNA was able to partially silence the expression of TREM-1 protein and remarkably inhibited TNF-α and IL-8 production in U937 foam cells, suggesting that TREM-1 is a positive regulator of TNF-α and IL-8 production in U937 foam cells. Our finding that TREM-1 controls the production of IL-8 and TNF-α in U937 foam cells defines a potentially critical role of TREM-1 in the pathogenesis of atherosclerosis and implicates TREM-1 as a potential therapeutic target for the disease.

摘要

我们的研究目的是探讨髓系细胞触发受体-1(TREM-1)在 U937 泡沫细胞中的表达水平,并确定 TREM-1 是否调节这些细胞中肿瘤坏死因子-α(TNF-α)和白细胞介素-8(IL-8)的产生。用佛波醇 12-肉豆蔻酸 13-乙酸酯孵育人 U937 细胞,然后用氧化型人低密度脂蛋白诱导泡沫细胞形成。用油红 O 染色鉴定泡沫细胞。通过酶联免疫吸附试验测定 U937 泡沫细胞中 IL-8 和 TNF-α的产生。用逆转录聚合酶链反应检测 U937 泡沫细胞中 TREM-1 mRNA 的表达。此外,用 Lipofectamine 2000 转染小干扰 RNA 使 U937 泡沫细胞沉默 TREM-1。用 Western blot 测定 TREM-1 蛋白表达,用 ELISA 检测 TREM-1 沉默对 IL-8 和 TNF-α产生的影响。PMA 和 ox-LDL 诱导 U937 细胞形成泡沫细胞。发现 U937 泡沫细胞中 TNF-α和 IL-8 的产生明显升高,同时 TREM-1 mRNA 明显上调。TREM-1 siRNA 能够部分沉默 TREM-1 蛋白的表达,并显著抑制 U937 泡沫细胞中 TNF-α和 IL-8 的产生,表明 TREM-1 是 U937 泡沫细胞中 TNF-α和 IL-8 产生的正调节因子。我们的研究结果表明,TREM-1 控制 U937 泡沫细胞中 IL-8 和 TNF-α的产生,这定义了 TREM-1 在动脉粥样硬化发病机制中的潜在关键作用,并暗示 TREM-1 是该疾病的潜在治疗靶点。

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