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萝卜硫素通过抑制线粒体蛋白氧化和补体 C3 的激活促进衣原体感染。

Sulforaphane promotes chlamydial infection by suppressing mitochondrial protein oxidation and activation of complement C3.

机构信息

Department of Internal Medicine, Section on Molecular Medicine, Wake Forest School of Medicine, Winston-Salem, 27157, North Carolina.

Department of Biology, Wake Forest University, Winston-Salem, 27015, North Carolina.

出版信息

Protein Sci. 2019 Jan;28(1):216-227. doi: 10.1002/pro.3536.

Abstract

Sulforaphane (SFN), a phytochemical found in broccoli and other cruciferous vegetables, is a potent antioxidant and anti-inflammatory agent with reported effects in cancer chemoprevention and suppression of infection with intracellular pathogens. Here we report on the impact of SFN on infection with Chlamydia trachomatis (Ct), a common sexually transmitted pathogen responsible for 131 million new cases annually worldwide. Astoundingly, we find that SFN as well as broccoli sprouts extract (BSE) promote Ct infection of human host cells. Both the number and size of Ct inclusions were increased when host cells were pretreated with SFN or BSE. The initial investigations presented here point to both the antioxidant and thiol alkylating properties of SFN as regulators of Ct infection. SFN decreased mitochondrial protein sulfenylation and promoted Ct development, which were both reversed by treatment with mitochondria-targeted paraquat (MitoPQ). Inhibition of the complement component 3 (complement C3) by SFN was also identified as a mechanism by which SFN promotes Ct infections. Mass spectrometry analysis found alkylation of cysteine 1010 (Cys1010) in complement C3 by SFN. The studies reported here raise awareness of the Ct infection promoting activity of SFN, and also identify potential mechanisms underlying this activity.

摘要

萝卜硫素(SFN)是一种存在于西兰花和其他十字花科蔬菜中的植物化学物质,具有抗氧化和抗炎作用,已被报道具有抗癌化学预防和抑制细胞内病原体感染的作用。在这里,我们报告了 SFN 对沙眼衣原体(Ct)感染的影响,Ct 是一种常见的性传播病原体,每年在全球导致 1.31 亿例新病例。令人惊讶的是,我们发现 SFN 以及西兰花芽提取物(BSE)促进了 Ct 感染宿主细胞。当宿主细胞用 SFN 或 BSE 预处理时,Ct 包涵体的数量和大小都增加了。这里呈现的初步研究表明,SFN 的抗氧化和硫醇烷化特性均可以调节 Ct 感染。SFN 降低了线粒体蛋白的亚磺化水平,并促进了 Ct 的发展,而用靶向线粒体的百草枯(MitoPQ)处理则可以逆转这一过程。SFN 通过抑制补体成分 3(补体 C3)也被鉴定为促进 Ct 感染的机制之一。质谱分析发现 SFN 对补体 C3 中的半胱氨酸 1010(Cys1010)进行了烷化。本研究报告提高了对 SFN 促进 Ct 感染活性的认识,并确定了这种活性的潜在机制。

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