巨噬细胞极化
巨噬细胞
免疫系统
生物
安普克
先天免疫系统
癌症免疫疗法
细胞生物学
信号转导
PI3K/AKT/mTOR通路
重编程
巨噬细胞激活因子
免疫
肿瘤微环境
免疫疗法
免疫学
细胞
磷酸化
生物化学
淋巴因子
蛋白激酶A
体外
作者
Shiyao Wang,Ruichen Liu,Qing Yu,Dong Lin,Yujing Bi,Guangwei Liu
出处
期刊:Cancer Letters
[Elsevier BV]
日期:2019-03-21
卷期号:452: 14-22
被引量:175
标识
DOI:10.1016/j.canlet.2019.03.015
摘要
In response to different microenvironmental stimuli, macrophages are polarized into two populations, M1 macrophages which are classically activated by interferon (IFN)-γ with lipopolysaccharides (LPSs) and M2 macrophages which are alternatively activated by interleukin-4 (IL-4), to perform specific roles in innate immune responses. Accordingly, macrophages occupy distinct metabolic profiles, regulated by orchestrated factors and signaling pathways, including the PI3K-AKT, HIF, c-Myc, AMPK, and PPARs pathways. These factors and pathways play pivotal roles not only in metabolic regulation but also in macrophage polarization. After activation, classically activated M1 macrophages and alternatively activated M2 macrophages display distinct patterns in glucose, lipid, amino acid and iron metabolism. Here, we summarized recently discovered metabolism-related inflammatory signaling factors, along with reprogrammed metabolism, after the activation of macrophages under conditions related to immunity and cancer. Additionally, macrophage regulatory roles in infectious diseases, cancer progression and anti-cancer immunotherapy are discussed in terms of metabolic profiles, providing insight into the prevention and treatment of immune-associated diseases.
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