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鞘氨醇-1-磷酸(S-1P)促进幼稚巨噬细胞分化并增强针对 的保护性免疫。

Sphingosine-1-Phosphate (S-1P) Promotes Differentiation of Naive Macrophages and Enhances Protective Immunity Against .

机构信息

Laboratory of Translational Medicine, School of Life Science, University of Hyderabad, Hyderabad, India.

Department of Experimental Animal Facility, National JALMA Institute for Leprosy and Other Mycobacterial Disease, Agra, India.

出版信息

Front Immunol. 2020 Jan 24;10:3085. doi: 10.3389/fimmu.2019.03085. eCollection 2019.

Abstract

Sphingosine-1-phosphate (S-1P) is a key sphingolipid involved in the pathobiology of various respiratory diseases. We have previously demonstrated the significance of S-1P in controlling non-pathogenic mycobacterial infection in macrophages, and here we demonstrate the therapeutic potential of S-1P against pathogenic (H37Rv) in the mouse model of infection. Our study revealed that S-1P is involved in the expression of iNOS proteins in macrophages, their polarization toward M1 phenotype, and secretion of interferon (IFN)-γ during the course of infection. S-1P is also capable of enhancing infiltration of pulmonary CD11b+ macrophages and expression of S-1P receptor-3 (S-1PR3) in the lungs during the course of infection. We further revealed the influence of S-1P on major signaling components of inflammatory signaling pathways during infection, thus highlighting antimycobacterial potential of S-1P in animals. Our data suggest that enhancing S-1P levels by sphingolipid mimetic compounds/drugs can be used as an immunoadjuvant for boosting immunity against pathogenic mycobacteria.

摘要

鞘氨醇-1-磷酸(S-1P)是一种参与多种呼吸道疾病病理生物学的关键鞘脂。我们之前已经证明了 S-1P 在控制巨噬细胞中非致病性分枝杆菌感染中的重要性,在这里,我们证明了 S-1P 在感染的小鼠模型中对致病性(H37Rv)的治疗潜力。我们的研究表明,S-1P 参与了感染过程中巨噬细胞中诱导型一氧化氮合酶(iNOS)蛋白的表达、向 M1 表型的极化以及干扰素(IFN)-γ的分泌。S-1P 还能够增强肺部 CD11b+巨噬细胞的浸润和 S-1P 受体-3(S-1PR3)在肺部的表达。我们进一步揭示了 S-1P 在感染过程中对炎症信号通路主要信号成分的影响,从而突出了 S-1P 在动物中的抗分枝杆菌潜力。我们的数据表明,通过鞘脂类似物/药物增强 S-1P 水平可以用作免疫佐剂,以增强对致病性分枝杆菌的免疫力。

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