MicroRNAs: At the Interface of Metabolic Pathways and Inflammatory Responses by Macrophages

被引:26
作者
Nelson, Morgan C. [1 ,2 ]
O'Connell, Ryan M. [1 ,2 ]
机构
[1] Univ Utah, Dept Pathol, Div Microbiol & Immunol, Salt Lake City, UT 84112 USA
[2] Univ Utah, Huntsman Canc Inst, Salt Lake City, UT 84112 USA
来源
FRONTIERS IN IMMUNOLOGY | 2020年 / 11卷
关键词
microRNA; metabolism; macrophage; immunometabolism; inflammation; macrophage polarization; TUMOR-ASSOCIATED MACROPHAGES; NITRIC-OXIDE; SUCCINATE-DEHYDROGENASE; ALTERNATIVE ACTIVATION; IMMUNE-RESPONSE; INNATE IMMUNITY; IN-VIVO; CELL; POLARIZATION; CANCER;
D O I
10.3389/fimmu.2020.01797
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Macrophages are key cells of the innate immune system with functional roles in both homeostatic maintenance of self-tissues and inflammatory responses to external stimuli, including infectious agents. Recent advances in metabolic research have revealed that macrophage functions rely upon coordinated metabolic programs to regulate gene expression, inflammation, and other important cellular processes. Polarized macrophages adjust their use of nutrients such as glucose and amino acids to meet their changing metabolic needs, and this in turn supports the functions of the activated macrophage. Metabolic and inflammatory processes have been widely studied, and a crucial role for their regulation at the post-transcriptional level by microRNAs (miRNAs) has been identified. miRNAs govern many facets of macrophage biology, including direct targeting of metabolic regulators and inflammatory pathways. This review will integrate emerging data that support an interplay between miRNAs and metabolism during macrophage inflammatory responses, highlighting critical miRNAs and miRNA families. Additionally, we will address the implications of these networks for human disease and discuss emerging areas of research in this field.
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页数:13
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