Glycosylation as a dynamic regulator of RLR and cGAS-STING innate immune signalling pathways

Innate immune sensing by RIG-I-like receptors (RLRs) and the cGAS-STING pathway is tightly regulated by glycosylation. This review summarizes how distinct glycosylation modalities shape antiviral signaling at multiple levels. N-glycosylation in the ER-Golgi is essential for STING folding, stability, and signaling competence, whereas aberrant glycan states disrupt DNA sensing. In contrast, cytosolic O-GlcNAcylation dynamically modulates RLR-cGAS pathways by regulating MAVS aggregation, suppressing IRF3 and NF-κB activation, and interfering with cGAS-DNA binding. We further discuss crosstalk between glycosylation, ubiquitination, and phosphorylation, metabolic regulation of UDP-GlcNAc flux, and pathogen- or tumor-driven glycosylation reprogramming, highlighting glycosylation enzymes as potential immunomodulatory targets.

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Publication Details

Journal
Communications Biology
Published
2026-03-24
DOI
https://doi.org/10.1038/s42003-026-09767-9
Primary Topic
interferon and immune responses
Type
article
Field-Weighted Citation Impact
0.00
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article

Glycosylation as a dynamic regulator of RLR and cGAS-STING innate immune signalling pathways

Communications Biology
interferon and immune responses
article

Glycosylation as a dynamic regulator of RLR and cGAS-STING innate immune signalling pathways

article en

Abstract

Innate immune sensing by RIG-I-like receptors (RLRs) and the cGAS-STING pathway is tightly regulated by glycosylation. This review summarizes how distinct glycosylation modalities shape antiviral signaling at multiple levels. N-glycosylation in the ER-Golgi is essential for STING folding, stability, and signaling competence, whereas aberrant glycan states disrupt DNA sensing. In contrast, cytosolic O-GlcNAcylation dynamically modulates RLR-cGAS pathways by regulating MAVS aggregation, suppressing IRF3 and NF-κB activation, and interfering with cGAS-DNA binding. We further discuss crosstalk between glycosylation, ubiquitination, and phosphorylation, metabolic regulation of UDP-GlcNAc flux, and pathogen- or tumor-driven glycosylation reprogramming, highlighting glycosylation enzymes as potential immunomodulatory targets.

Communications BiologyVol. 9(1)
Hebei Agricultural University (CN), Henan University of Traditional Chinese Medicine (CN), University of Calgary (CA), Second Affiliated Hospital of Zhengzhou University (CN), Hebei University (CN)
Openalex Percentile: Top 9%
interferon and immune responses
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