4.7 Review

Impact of intracellular innate immune receptors on immunometabolism

Journal

CELLULAR & MOLECULAR IMMUNOLOGY
Volume 19, Issue 3, Pages 337-351

Publisher

CHIN SOCIETY IMMUNOLOGY
DOI: 10.1038/s41423-021-00780-y

Keywords

Immunometabolism; NLRs; NLRP3; AIM2 inflammasomes; innate sensors; receptors; STING; AKT-mTOR

Categories

Funding

  1. NIH [R35 CA232109, PO1 DK094779, U19 AI067798, R01 AI141333, R01 AI029564]

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Immunometabolism plays a crucial role in regulating immune cell functions, with the interaction between PI3K-AKT-mTOR and LKB1-AMPK signaling pathways being essential for modulating cell metabolism. Intracellular innate immune sensors/receptors have a significant impact on metabolic pathways, highlighting the need for further investigation into their mechanisms of interaction.
Immunometabolism, which is the metabolic reprogramming of anaerobic glycolysis, oxidative phosphorylation, and metabolite synthesis upon immune cell activation, has gained importance as a regulator of the homeostasis, activation, proliferation, and differentiation of innate and adaptive immune cell subsets that function as key factors in immunity. Metabolic changes in epithelial and other stromal cells in response to different stimulatory signals are also crucial in infection, inflammation, cancer, autoimmune diseases, and metabolic disorders. The crosstalk between the PI3K-AKT-mTOR and LKB1-AMPK signaling pathways is critical for modulating both immune and nonimmune cell metabolism. The bidirectional interaction between immune cells and metabolism is a topic of intense study. Toll-like receptors (TLRs), cytokine receptors, and T and B cell receptors have been shown to activate multiple downstream metabolic pathways. However, how intracellular innate immune sensors/receptors intersect with metabolic pathways is less well understood. The goal of this review is to examine the link between immunometabolism and the functions of several intracellular innate immune sensors or receptors, such as nucleotide-binding and leucine-rich repeat-containing receptors (NLRs, or NOD-like receptors), absent in melanoma 2 (AIM2)-like receptors (ALRs), and the cyclic dinucleotide receptor stimulator of interferon genes (STING). We will focus on recent advances and describe the impact of these intracellular innate immune receptors on multiple metabolic pathways. Whenever appropriate, this review will provide a brief contextual connection to pathogenic infections, autoimmune diseases, cancers, metabolic disorders, and/or inflammatory bowel diseases.

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