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大蒜素增强巨噬细胞的抗分枝杆菌活性。

Enhancement of the antimycobacterial activity of macrophages by ajoene.

机构信息

1 Department of Medical Science, College of Medicine, Chungnam National University, Daejeon, South Korea.

2 Department of Microbiology, College of Medicine, Chungnam National University, Daejeon, South Korea.

出版信息

Innate Immun. 2018 Jan;24(1):79-88. doi: 10.1177/1753425917747975. Epub 2017 Dec 14.

Abstract

Ajoene, a garlic-derived sulfur-containing compound, has broad-spectrum antimicrobial activity. To assess the potential of ajoene for treating tuberculosis (TB), we determined whether it induces the stress response of the endoplasmic reticulum (ER), which plays an important role in TB. We showed that ajoene stimulation induced the production of ER stress sensor molecules and reactive oxygen species (ROS) levels. Ajoene-induced ROS production was dependent on c-Jun N-terminal kinase (JNK) activation. Interestingly, the inhibition of JNK activity and suppression of ROS production reduced ajoene-induced CHOP production in macrophages. Because ER stress activates autophagy, the activation of which suppresses the growth of mycobacteria, we investigated the ajoene-induced production of autophagy-related factors, including LC3-II, P62 and Beclin-1. As expected, ajoene treatment increased the levels of these factors in RAW 264.7 cells. Remarkably, the total amount of Mycobacterium tuberculosis (Mtb) H37Rv was significantly reduced in ajoene-treated RAW 264.7 cells. The treatment of macrophages with ajoene resulted in the activation of JNK, induction of ROS synthesis and accumulation of ROS, possibly leading to the activation of ER stress and autophagy. These results reveal the mechanism of the antimycobacterial effects of ajoene against Mtb H37Rv. Our findings might facilitate the development of novel therapies for patients with TB.

摘要

大蒜衍生的含硫化合物——ajoene 具有广谱抗菌活性。为评估 ajoene 治疗结核病(TB)的潜力,我们确定其是否能诱导内质网(ER)的应激反应,而 ER 在 TB 中起着重要作用。我们发现 ajoene 刺激诱导了 ER 应激传感器分子的产生和活性氧(ROS)水平的升高。Ajoene 诱导的 ROS 产生依赖于 c-Jun N-末端激酶(JNK)的激活。有趣的是,JNK 活性的抑制和 ROS 产生的抑制降低了巨噬细胞中 ajoene 诱导的 CHOP 产生。由于 ER 应激会激活自噬,而自噬的激活会抑制分枝杆菌的生长,因此我们研究了 ajoene 诱导的自噬相关因子的产生,包括 LC3-II、P62 和 Beclin-1。不出所料,Ajoene 处理增加了 RAW 264.7 细胞中这些因子的水平。值得注意的是,Ajoene 处理的 RAW 264.7 细胞中结核分枝杆菌(Mtb)H37Rv 的总量明显减少。巨噬细胞用 ajoene 处理会导致 JNK 的激活、ROS 合成和积累的诱导,这可能导致 ER 应激和自噬的激活。这些结果揭示了 ajoene 对 Mtb H37Rv 的抗分枝杆菌作用的机制。我们的研究结果可能有助于为 TB 患者开发新的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aaf9/6830758/5550cde35c0a/10.1177_1753425917747975-fig1.jpg

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