NF-κB in monocytes and macrophages – an inflammatory master regulator in multitalented immune cells

生物 细胞生物学 先天免疫系统 转录因子 炎症体 趋化因子 免疫系统 巨噬细胞极化 炎症 NF-κB 免疫学 调节器 促炎细胞因子 细胞因子 信号转导 巨噬细胞 遗传学 体外 基因
作者
Marion Mußbacher,Martina Derler,José Basílio,Johannes A. Schmid
出处
期刊:Frontiers in Immunology [Frontiers Media]
卷期号:14 被引量:115
标识
DOI:10.3389/fimmu.2023.1134661
摘要

Nuclear factor κB (NF-κB) is a dimeric transcription factor constituted by two of five protein family members. It plays an essential role in inflammation and immunity by regulating the expression of numerous chemokines, cytokines, transcription factors, and regulatory proteins. Since NF-κB is expressed in almost all human cells, it is important to understand its cell type-, tissue-, and stimulus-specific roles as well as its temporal dynamics and disease-specific context. Although NF-κB was discovered more than 35 years ago, many questions are still unanswered, and with the availability of novel technologies such as single-cell sequencing and cell fate-mapping, new fascinating questions arose. In this review, we will summarize current findings on the role of NF-κB in monocytes and macrophages. These innate immune cells show high plasticity and dynamically adjust their effector functions against invading pathogens and environmental cues. Their versatile functions can range from antimicrobial defense and antitumor immune responses to foam cell formation and wound healing. NF-κB is crucial for their activation and balances their phenotypes by finely coordinating transcriptional and epigenomic programs. Thereby, NF-κB is critically involved in inflammasome activation, cytokine release, and cell survival. Macrophage-specific NF-κB activation has far-reaching implications in the development and progression of numerous inflammatory diseases. Moreover, recent findings highlighted the temporal dynamics of myeloid NF-κB activation and underlined the complexity of this inflammatory master regulator. This review will provide an overview of the complex roles of NF-κB in macrophage signal transduction, polarization, inflammasome activation, and cell survival.
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