Xinfeng capsule attenuates ankylosing spondylitis by downregulating YTHDC1-mediated m6A modification of LINC01579 and suppressing IL-17/NF-κB signaling

Background: A-dependent epigenetic mechanisms remains unclear. Objective: A modification. Methods: A levels were quantified by MeRIP-qPCR. Inflammation and pathway activation were assessed via immunofluorescence, Western blot, and enzyme-linked immunosorbent assay (ELISA). RNA stability was evaluated using actinomycin D assays, while cell migration was measured by scratch assays. Bone destruction was analyzed using micro-CT and histological staining. Additionally, an IL-17 pathway inhibitor (AIN457) and agonist (SR0987) were employed to validate pathway involvement. Results: , XFC ameliorated joint inflammation, bone erosion, and joint space narrowing in PGIA mice. Conclusion: XFC alleviates AS progression by inhibiting YTHDC1-mediated m6A modification of LINC01579, which prevents its degradation and subsequently dampens IL-17/NF-κB pathway activation. These findings highlight a potential epigenetic mechanism underlying the therapeutic effects of XFC in AS.

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Journal
Frontiers in Immunology
Published
2026-04-16
DOI
https://doi.org/10.3389/fimmu.2026.1762062
Primary Topic
RNA modifications and cancer
Type
article
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0.00
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article

Xinfeng capsule attenuates ankylosing spondylitis by downregulating YTHDC1-mediated m6A modification of LINC01579 and suppressing IL-17/NF-κB signaling

Xian-heng Zhang, X W Chen, Jian Liu, Yanyan Fang et al.
Frontiers in Immunology
RNA modifications and cancer
article

Xinfeng capsule attenuates ankylosing spondylitis by downregulating YTHDC1-mediated m6A modification of LINC01579 and suppressing IL-17/NF-κB signaling

Xian-heng Zhang, X W Chen, Jian Liu, Yanyan Fang, Xiang Ding
article en

Abstract

Background: A-dependent epigenetic mechanisms remains unclear. Objective: A modification. Methods: A levels were quantified by MeRIP-qPCR. Inflammation and pathway activation were assessed via immunofluorescence, Western blot, and enzyme-linked immunosorbent assay (ELISA). RNA stability was evaluated using actinomycin D assays, while cell migration was measured by scratch assays. Bone destruction was analyzed using micro-CT and histological staining. Additionally, an IL-17 pathway inhibitor (AIN457) and agonist (SR0987) were employed to validate pathway involvement. Results: , XFC ameliorated joint inflammation, bone erosion, and joint space narrowing in PGIA mice. Conclusion: XFC alleviates AS progression by inhibiting YTHDC1-mediated m6A modification of LINC01579, which prevents its degradation and subsequently dampens IL-17/NF-κB pathway activation. These findings highlight a potential epigenetic mechanism underlying the therapeutic effects of XFC in AS.

Frontiers in ImmunologyVol. 17
Anhui University of Traditional Chinese Medicine (CN)
Good health and well-being
Openalex Percentile: Top 22%
RNA modifications and cancer
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