炎症
生物
促炎细胞因子
炎症体
免疫系统
背景(考古学)
细胞生物学
先天免疫系统
信号转导
免疫
免疫学
获得性免疫系统
功能(生物学)
下调和上调
基因
遗传学
古生物学
作者
Runliu Wu,Jiao Liu,Daolin Tang,Rui Kang
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:2023-08-07
卷期号:211 (4): 518-526
被引量:15
标识
DOI:10.4049/jimmunol.2300101
摘要
Immunometabolism is an interdisciplinary field that focuses on the relationship between metabolic pathways and immune responses. Dysregulated immunometabolism contributes to many pathological settings, such as cytokine storm or immune tolerance. Aconitate decarboxylase 1 (ACOD1, also known as immunoresponsive gene 1), the mitochondrial enzyme responsible for catalyzing itaconate production, was originally identified as a bacterial LPS-inducible gene involved in innate immunity in mouse macrophages. We now know that the upregulation of ACOD1 expression in immune or nonimmune cells plays a context-dependent role in metabolic reprogramming, signal transduction, inflammasome regulation, and protein modification. The emerging function of ACOD1 in inflammation and infection is a double-edged sword. In this review, we discuss how ACOD1 regulates anti-inflammatory or proinflammatory responses in an itaconate-dependent or -independent manner. Further understanding of ACOD1 expression and function may pave the way for the development of precision therapies for inflammatory diseases.
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