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血管生成素样蛋白2诱导腹膜细胞产生促炎反应。

Angiopoietin-like protein 2 induces proinflammatory responses in peritoneal cells.

作者信息

Umikawa Masato, Umikawa Asako, Asato Tsuyoshi, Takei Kimiko, Matsuzaki Goro, Kariya Ken-ichi, Zhang Cheng Cheng

机构信息

Department of Medical Biochemistry, Graduate School of Medicine, University of the Ryukyus, Okinawa, Japan.

Department of Medical Biochemistry, Graduate School of Medicine, University of the Ryukyus, Okinawa, Japan.

出版信息

Biochem Biophys Res Commun. 2015 Nov 13;467(2):235-41. doi: 10.1016/j.bbrc.2015.09.183. Epub 2015 Oct 3.

Abstract

Monocytes and macrophages are important effectors and regulators of inflammation, and both their differentiation and activation are regulated strictly in response to environmental cues. Angiopoietin-like protein 2 (Angptl2) is a multifaceted protein, displaying many physiological and pathological functions in inflammation, angiogenesis, hematopoiesis, and tumor development. Although recent studies implicate Angptl2 in chronic inflammation, the mechanisms of inflammation caused by Angptl2 remain unclear. The purpose of the present study was to elucidate the role of Angptl2 in inflammation by understanding the effects of Angptl2 on monocytes/macrophages. We showed that Angptl2 directly activates resident murine peritoneal monocytes and macrophages and induces a drastic upregulation of the transcription of several inflammatory genes including nitric oxide synthase 2 and prostaglandin-endoperoxide synthase 2, and several proinflammatory cytokine genes such as interleukin (IL)-1β, IL-6, TNFα, and CSF2, along with activation of ERK, JNK, p38, and nuclear factor kappa B signaling pathways. Concordantly, proinflammatory cytokines IL-1β, IL-6, TNFα, and GM-CSF, were rapidly elevated from murine peritoneal monocytes and macrophages. These results demonstrate a novel role for Angptl2 in inflammation via the direct activation of peritoneal monocytes and macrophages.

摘要

单核细胞和巨噬细胞是炎症的重要效应器和调节因子,它们的分化和激活均严格受环境信号调控。血管生成素样蛋白2(Angptl2)是一种多功能蛋白,在炎症、血管生成、造血及肿瘤发展过程中发挥着多种生理和病理功能。尽管近期研究表明Angptl2与慢性炎症有关,但其引发炎症的机制仍不清楚。本研究旨在通过了解Angptl2对单核细胞/巨噬细胞的影响,阐明Angptl2在炎症中的作用。我们发现,Angptl2可直接激活驻留的小鼠腹腔单核细胞和巨噬细胞,并诱导包括一氧化氮合酶2和前列腺素内过氧化物合酶2在内的多种炎症基因以及白细胞介素(IL)-1β、IL-6、肿瘤坏死因子α(TNFα)和集落刺激因子2(CSF2)等多种促炎细胞因子基因的转录大幅上调,同时激活细胞外信号调节激酶(ERK)、c-Jun氨基末端激酶(JNK)、p38和核因子κB信号通路。相应地,促炎细胞因子IL-1β、IL-6、TNFα和粒细胞-巨噬细胞集落刺激因子(GM-CSF)在小鼠腹腔单核细胞和巨噬细胞中迅速升高。这些结果表明,Angptl2通过直接激活腹腔单核细胞和巨噬细胞在炎症中发挥新的作用。

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