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本文引用的文献

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Macrophage activation and polarization: nomenclature and experimental guidelines.巨噬细胞激活与极化:命名及实验指南
Immunity. 2014 Jul 17;41(1):14-20. doi: 10.1016/j.immuni.2014.06.008.
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The M1 and M2 paradigm of macrophage activation: time for reassessment.巨噬细胞活化的M1和M2范式:是时候重新评估了。
F1000Prime Rep. 2014 Mar 3;6:13. doi: 10.12703/P6-13. eCollection 2014.
3
A critical role for suppressor of cytokine signalling 3 in promoting M1 macrophage activation and function in vitro and in vivo.细胞因子信号转导抑制因子 3 在体外和体内促进 M1 巨噬细胞激活和功能中的关键作用。
Immunology. 2014 Jan;141(1):96-110. doi: 10.1111/imm.12173.
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Macrophages control innate inflammation.巨噬细胞控制先天炎症。
Diabetes Obes Metab. 2013 Sep;15 Suppl 3:10-8. doi: 10.1111/dom.12151.
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The adenosine-dependent angiogenic switch of macrophages to an M2-like phenotype is independent of interleukin-4 receptor alpha (IL-4Rα) signaling.巨噬细胞中依赖于腺苷的血管生成开关向 M2 样表型的转换不依赖于白细胞介素 4 受体 α(IL-4Rα)信号。
Inflammation. 2013 Aug;36(4):921-31. doi: 10.1007/s10753-013-9621-3.
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Genetic programs expressed in resting and IL-4 alternatively activated mouse and human macrophages: similarities and differences.静息状态和 IL-4 交替激活的小鼠和人巨噬细胞中表达的遗传程序:相似性和差异性。
Blood. 2013 Feb 28;121(9):e57-69. doi: 10.1182/blood-2012-06-436212. Epub 2013 Jan 4.
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Fra-1 protooncogene regulates IL-6 expression in macrophages and promotes the generation of M2d macrophages.Fra-1 原癌基因调节巨噬细胞中 IL-6 的表达,并促进 M2d 巨噬细胞的生成。
Cell Res. 2010 Jun;20(6):701-12. doi: 10.1038/cr.2010.52. Epub 2010 Apr 13.
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Glucocorticoids induce differentiation of a specifically activated, anti-inflammatory subtype of human monocytes.糖皮质激素可诱导人单核细胞中一种特异性活化的抗炎亚型的分化。
Blood. 2007 Feb 1;109(3):1265-74. doi: 10.1182/blood-2006-02-001115. Epub 2006 Oct 3.
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Regulation of macrophage phenotype by long-term exposure to IL-10.长期暴露于白细胞介素-10对巨噬细胞表型的调节作用。
Immunobiology. 2005;210(2-4):77-86. doi: 10.1016/j.imbio.2005.05.002.
10
The chemokine system in diverse forms of macrophage activation and polarization.不同形式巨噬细胞活化与极化中的趋化因子系统
Trends Immunol. 2004 Dec;25(12):677-86. doi: 10.1016/j.it.2004.09.015.

体外极化巨噬细胞。

Polarizing Macrophages In Vitro.

作者信息

Huang Xuan, Li Yong, Fu Mingui, Xin Hong-Bo

机构信息

Institute of Translational Medicine, Nanchang University, Nanchang, People's Republic of China.

Department of Biomedical Science and Shock, Trauma Research Center, School of Medicine, University of Missouri Kansas City, Kansas City, MO, USA.

出版信息

Methods Mol Biol. 2018;1784:119-126. doi: 10.1007/978-1-4939-7837-3_12.

DOI:10.1007/978-1-4939-7837-3_12
PMID:29761394
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8875934/
Abstract

Macrophages are a heterogeneous population of innate myeloid cells involved in health and disease, which are the most functionally diverse cells of the hematopoietic system. The main functions of macrophages include responding to pathogens and modulating the adaptive immune response, induction and resolution of inflammation, tissue repair, and homeostasis. Macrophages exhibit remarkable plasticity, in which the different populations of macrophages with distinct physiological and pathological roles can be developed in response to different stimuli. Depending on the types of stimuli that macrophages are exposed to, these cells will be able to polarize to M1 (pro-inflammatory) or M2 (anti-inflammatory) macrophages. M1 macrophages are induced by stimulation with IFNγ and LPS. Based on the stimuli and the achieved transcriptional changes, the M2 macrophages can be classified into four subdivisions: alternative activated macrophages (M2a, activated by IL-4 or IL-13), type 2 macrophages (M2b, activated by immune complexes and LPS), deactivated macrophages (M2c, activated by glucocorticoids or IL-10), and M2-like macrophages (M2d, activated by adenosines or IL-6). In this chapter, we describe the methods to generate different phenotypes of activated macrophages by adding certain stimuli and we also summarize the distinct markers and/or cytokines used for verification of each activated macrophage.

摘要

巨噬细胞是参与健康与疾病的异质性固有髓系细胞群体,是造血系统中功能最为多样的细胞。巨噬细胞的主要功能包括对病原体作出反应并调节适应性免疫反应、诱导和消除炎症、组织修复以及维持体内平衡。巨噬细胞具有显著的可塑性,能够根据不同刺激产生具有不同生理和病理作用的不同巨噬细胞群体。根据巨噬细胞所接触的刺激类型,这些细胞能够极化为M1(促炎)或M2(抗炎)巨噬细胞。M1巨噬细胞由IFNγ和LPS刺激诱导产生。基于刺激因素和所实现的转录变化,M2巨噬细胞可分为四个亚群:替代性活化巨噬细胞(M2a,由IL-4或IL-13活化)、2型巨噬细胞(M2b,由免疫复合物和LPS活化)、失活巨噬细胞(M2c,由糖皮质激素或IL-10活化)以及M2样巨噬细胞(M2d,由腺苷或IL-6活化)。在本章中,我们描述了通过添加特定刺激来产生不同表型活化巨噬细胞的方法,并且还总结了用于验证每种活化巨噬细胞的独特标志物和/或细胞因子。