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松柏醛通过白细胞中 ALOX15 的上调加剧 LPS 诱导的细胞凋亡。

Pinosylvin exacerbates LPS-induced apoptosis via ALOX 15 upregulation in leukocytes.

机构信息

Department of Molecular Biology & Institute of Nanosensor and Biotechnology, Dankook University, Cheonan 31116, Korea.

出版信息

BMB Rep. 2018 Jun;51(6):302-307. doi: 10.5483/bmbrep.2018.51.6.024.

Abstract

Pinosylvin is known to have anti-inflammatory activity in endothelial cells. In this study, we found that pinosylvin had a pro-apoptotic activity in lipopolysaccharide (LPS)-preconditioned leukocytes. This finding suggests that pinosylvin has an effect on the resolution of inflammation. To understand the detailed mechanism, we examined if pinosylvin enhances cyclooxygenase (COX) or lipoxygenase (LOX) activity in THP-1 and U937 cells. LOX activity was found to be markedly increased by pinosylvin, whereas COX activity was not altered. Furthermore, we found that pinosylvin enhanced both levels of ALOX 15 mRNA and protein, implying that LOX activity, elevated by pinosylvin, is attributed to upregulation of ALOX 15 expression. From this cell signaling study, pinosylvin appeared to promote phosphorylations of ERK and JNK. ERK or JNK inhibitors were found to attenuate ALOX 15 expression and LPS-induced apoptosis promoted by pinosylvin. In conclusion, pinosylvin enhances the apoptosis of LPSpreconditioned leukocytes by up-regulating ALOX 15 expression through ERK and JNK. These findings suggest that pinosylvin may induce the resolution of inflammation. [BMB Reports 2018; 51(6): 302-307].

摘要

松柏醇已知具有内皮细胞抗炎活性。在这项研究中,我们发现松柏醇在脂多糖 (LPS) 预处理的白细胞中有促凋亡活性。这一发现表明松柏醇对炎症的消退有影响。为了了解详细的机制,我们检查了松柏醇是否增强了 THP-1 和 U937 细胞中的环加氧酶 (COX) 或脂加氧酶 (LOX) 活性。发现松柏醇明显增加了 LOX 活性,而 COX 活性没有改变。此外,我们发现松柏醇增强了 ALOX 15 mRNA 和蛋白的水平,这意味着 LOX 活性的升高归因于 ALOX 15 表达的上调。从这个细胞信号研究中,松柏醇似乎促进了 ERK 和 JNK 的磷酸化。ERK 或 JNK 抑制剂被发现可以减弱由松柏醇诱导的 ALOX 15 表达和 LPS 诱导的凋亡。总之,松柏醇通过 ERK 和 JNK 上调 ALOX 15 表达,增强 LPS 预处理白细胞的凋亡。这些发现表明松柏醇可能诱导炎症的消退。[BMB 报告 2018;51(6):302-307]。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/568e/6033067/658667e4e0ff/bmb-51-302f1.jpg

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