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多胺在调节巨噬细胞极化和功能中的作用。

The role of polyamines in the regulation of macrophage polarization and function.

机构信息

Division of Gastroenterology, Hepatology and Nutrition, Department of Medicine, Vanderbilt University Medical Center, Vanderbilt University School of Medicine, 2215 Garland Avenue, Room 1030C Medical Research Building IV, Nashville, TN, 37232, USA.

Department of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN, USA.

出版信息

Amino Acids. 2020 Feb;52(2):151-160. doi: 10.1007/s00726-019-02719-0. Epub 2019 Apr 23.

Abstract

Naturally occurring polyamines are ubiquitously distributed and play important roles in cell development, amino acid and protein synthesis, oxidative DNA damage, proliferation, and cellular differentiation. Macrophages are essential in the innate immune response, and contribute to tissue remodeling. Naïve macrophages have two major potential fates: polarization to (1) the classical pro-inflammatory M1 defense response to bacterial pathogens and tumor cells, and (2) the alternatively activated M2 response, induced in the presence of parasites and wounding, and also implicated in the development of tumor-associated macrophages. ODC, the rate-limiting enzyme in polyamine synthesis, leads to an increase in putrescine levels, which impairs M1 gene transcription. Additionally, spermidine and spermine can regulate translation of pro-inflammatory mediators in activated macrophages. In this review, we focus on polyamines in macrophage activation patterns in the context of gastrointestinal inflammation and carcinogenesis. We seek to clarify mechanisms of innate immune regulation by polyamine metabolism and potential novel therapeutic targets.

摘要

天然存在的多胺广泛分布,在细胞发育、氨基酸和蛋白质合成、氧化 DNA 损伤、增殖和细胞分化中发挥重要作用。巨噬细胞在先天免疫反应中至关重要,并有助于组织重塑。幼稚巨噬细胞有两种主要的潜在命运:极化为 (1) 对细菌病原体和肿瘤细胞的经典促炎 M1 防御反应,和 (2) 替代激活的 M2 反应,在寄生虫和创伤存在的情况下诱导,也与肿瘤相关巨噬细胞的发展有关。多胺合成的限速酶 ODC 导致腐胺水平升高,从而损害 M1 基因转录。此外,亚精胺和精胺可以调节激活的巨噬细胞中促炎介质的翻译。在这篇综述中,我们重点讨论了多胺在胃肠道炎症和癌变中巨噬细胞激活模式中的作用。我们试图阐明多胺代谢对先天免疫调节的机制和潜在的新治疗靶点。

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