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1,6-O,O-二乙酰基britannilactone 通过抑制 STAT6 活化抑制 A549 细胞中 eotaxin-1 和 ALOX15 的表达。

1,6-O,O-Diacetylbritannilactone Inhibits Eotaxin-1 and ALOX15 Expression Through Inactivation of STAT6 in A549 Cells.

机构信息

Tianjin Key Laboratory on Technologies Enabling Development of Clinical Therapeutics and Diagnostics, School of Pharmacy, Tianjin Medical University, Tianjin, 300070, China.

Tianjin Key Laboratory of Ophthalmology and Visual Science, Tianjin Eye Hospital, Tianjin, 300020, China.

出版信息

Inflammation. 2017 Dec;40(6):1967-1974. doi: 10.1007/s10753-017-0637-y.

Abstract

1,6-O,O-Diacetylbritannilactone (OODBL), a plant sesquiterpene lactone, was previously reported to show multiple pharmacological effects such as anti-cancer and anti-inflammatory activities. In this study, we investigated the anti-inflammatory effect of OODBL on interleukin (IL)-4-induced signal transducer and activator of transcription 6 (STAT6) signaling pathway in human lung A549 cells. We found that OODBL dramatically inhibited IL-4-induced messenger RNA (mRNA) expression of eotaxin-1 and arachidonate 15-lipoxygenase-1 (ALOX15) in a dose-dependent manner. To clarify the action mechanism of OODBL, we examined the effect of OODBL on activation of STAT6. OODBL decreased both STAT6 phosphorylation and reporter gene activity. Furthermore, OODBL suppressed phosphorylation of Janus Kinase 3 (JAK3) without affecting JAK1. Taken together, OODBL abolished IL-4-induced eotaxin-1 and ALOX15 mRNA expressions by repressing the activation of STAT6 and JAK3. These results suggest that OODBL has a potential therapeutic efficacy on inflammatory diseases especially allergic airway disease as a lead compound.

摘要

1,6-O,O-二乙酰基britannilactone(OODBL)是一种植物倍半萜内酯,先前的研究报道其具有多种药理作用,如抗癌和抗炎活性。在这项研究中,我们研究了 OODBL 对人肺 A549 细胞白细胞介素(IL)-4 诱导的信号转导和转录激活因子 6(STAT6)信号通路的抗炎作用。我们发现 OODBL 能够显著抑制 IL-4 诱导的 eotaxin-1 和花生四烯酸 15-脂氧合酶-1(ALOX15)mRNA 的表达,呈剂量依赖性。为了阐明 OODBL 的作用机制,我们研究了 OODBL 对 STAT6 激活的影响。OODBL 降低了 STAT6 磷酸化和报告基因活性。此外,OODBL 抑制了 Janus 激酶 3(JAK3)的磷酸化,而不影响 JAK1。综上所述,OODBL 通过抑制 STAT6 和 JAK3 的激活,消除了 IL-4 诱导的 eotaxin-1 和 ALOX15 mRNA 的表达。这些结果表明,OODBL 作为一种先导化合物,具有治疗炎症性疾病,特别是过敏性气道疾病的潜力。

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