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硫酸化维赞汀诱导巨噬细胞胞外诱捕网的形成。

Sulfated vizantin induces formation of macrophage extracellular traps.

作者信息

Oda Masataka, Kurosawa Mie, Yamamoto Hirofumi, Domon Hisanori, Kimura Tatsuya, Isono Toshihito, Maekawa Tomoki, Hayashi Naoki, Yamada Noriteru, Furue Yui, Kai Daichi, Terao Yutaka

机构信息

Division of Microbiology and Infectious Diseases, Graduate School ot Medical and Dental Sciences, Niigata University, 2-5274, Gakkocho-dori, Chuo-ku, Niigara, 95 l-8514, Japan.

Department of Microbiology and Infection Control Science, Kyoto Pharmaceutical University, 5 Misasagi, Yamashina, Kyoto, 607-8414, Japan.

出版信息

Microbiol Immunol. 2018 May;62(5):310-316. doi: 10.1111/1348-0421.12589.

Abstract

Vizantin is an insoluble adjuvant that activates macrophages and lymphocytes. Recently, 2,2',3,3',4,4'-hexasulfated-vizantin (sulfated vizantin), which enables solubilization of vizantin, was developed by the present team. Sulfated vizantin was found to enhance bactericidal activity against multi-drug resistant Pseudomonas aeruginosa in RAW264.7 cells. In addition, spread of P. aeruginosa was inhibited in RAW264.7 cells treated with sulfated vizantin. When only sulfated vizantin and P. aeruginosa were incubated, sulfated vizantin did not affect growth of P. aeruginosa. Formation of DNA-based extracellular traps (ETs), a novel defense mechanism in several types of innate immune cells, helps to eliminate pathogens. In the present study, ET-forming macrophages constituted the majority of immune cells. Sulfated vizantin induced ET formation in RAW264.7 cells, whereas a Ca-chelating reagent, EDTA, and T-type calcium channel blocker, tetrandrine, inhibited ET formation and attenuated inhibition of spread of P. aeruginosa in sulfated vizantin-treated cells. Thus, sulfated vizantin induces ET formation in phagocytic cells in a Ca-dependent manner, thus preventing spread of P. aeruginosa. Hence, sulfated vizantin may be useful in the management of infectious diseases.

摘要

维赞汀是一种可激活巨噬细胞和淋巴细胞的不溶性佐剂。最近,本团队研发出了2,2',3,3',4,4'-六硫酸化维赞汀(硫酸化维赞汀),它能使维赞汀溶解。研究发现硫酸化维赞汀可增强RAW264.7细胞对多重耐药铜绿假单胞菌的杀菌活性。此外,在用硫酸化维赞汀处理的RAW264.7细胞中,铜绿假单胞菌的扩散受到抑制。当仅将硫酸化维赞汀与铜绿假单胞菌一起孵育时,硫酸化维赞汀不会影响铜绿假单胞菌的生长。基于DNA的细胞外陷阱(ETs)的形成是几种先天免疫细胞中的一种新型防御机制,有助于清除病原体。在本研究中,形成ET的巨噬细胞构成了免疫细胞的主体。硫酸化维赞汀可诱导RAW264.7细胞形成ET,而一种钙螯合剂乙二胺四乙酸(EDTA)和T型钙通道阻滞剂粉防己碱可抑制ET形成,并减弱硫酸化维赞汀处理的细胞中对铜绿假单胞菌扩散的抑制作用。因此,硫酸化维赞汀以钙依赖的方式诱导吞噬细胞形成ET,从而阻止铜绿假单胞菌的扩散。因此,硫酸化维赞汀可能对传染病的治疗有用。

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