Histone deacetylase 6 inhibits STING-dependent antiviral immunity via site-specific deacetylation

Histone deacetylase HDAC6 is a critical regulator of antiviral innate immunity, but its precise molecular mechanisms during RNA viral infection remain incompletely understood. In this study, we demonstrate that HDAC6 depletion (via siRNA knockdown or pharmacological inhibition) significantly suppresses vesicular stomatitis virus (VSV) replication. Further analysis revealed that HDAC6 modulates innate immune signaling by targeting the stimulator of interferon genes (STING) pathway, thereby attenuating type I interferon (IFN) responses. Mechanistically, HDAC6 directly interacts with STING and catalyzes its deacetylation at lysine 338 (K338). This post-translational modification impedes TBK1 recruitment by altering STING acetylation status, ultimately impairing STING phosphorylation at serine 366 (S366). Functional validation showed that overexpression of a STING with K338Q acetylation-mimetic mutant confers cellular resistance to VSV infection, establishing HDAC6-mediated STING deacetylation as a pivotal regulatory checkpoint in the antiviral response.

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Publication Details

Journal
Journal of Biological Chemistry
Published
2025-10-23
DOI
https://doi.org/10.1016/j.jbc.2025.110841
Citations
1
Primary Topic
interferon and immune responses
Type
article
Field-Weighted Citation Impact
0.80
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article

Histone deacetylase 6 inhibits STING-dependent antiviral immunity via site-specific deacetylation

Xiangwei Wang, Berihun Afera, Yuefeng Sun, Jianlin Han et al.
1 citations
Journal of Biological Chemistry
interferon and immune responses
0.80
article

Histone deacetylase 6 inhibits STING-dependent antiviral immunity via site-specific deacetylation

Xiangwei Wang, Berihun Afera, Yuefeng Sun, Jianlin Han, Miaomiao Li, Xiangping Yin, Min Qu, Pengyuan Cheng, Ke Guo, Yiyuan Ma, Dali Wei, Qunhua Ke
article en
1 citations

Abstract

Histone deacetylase HDAC6 is a critical regulator of antiviral innate immunity, but its precise molecular mechanisms during RNA viral infection remain incompletely understood. In this study, we demonstrate that HDAC6 depletion (via siRNA knockdown or pharmacological inhibition) significantly suppresses vesicular stomatitis virus (VSV) replication. Further analysis revealed that HDAC6 modulates innate immune signaling by targeting the stimulator of interferon genes (STING) pathway, thereby attenuating type I interferon (IFN) responses. Mechanistically, HDAC6 directly interacts with STING and catalyzes its deacetylation at lysine 338 (K338). This post-translational modification impedes TBK1 recruitment by altering STING acetylation status, ultimately impairing STING phosphorylation at serine 366 (S366). Functional validation showed that overexpression of a STING with K338Q acetylation-mimetic mutant confers cellular resistance to VSV infection, establishing HDAC6-mediated STING deacetylation as a pivotal regulatory checkpoint in the antiviral response.

Journal of Biological ChemistryVol. 301(12)
Nanjing Agricultural University (CN), Gansu Agricultural University (CN), Lanzhou Institute of Chemical Physics (CN), Lanzhou Veterinary Research Institute (CN), Chinese Academy of Agricultural Sciences (CN), Gansu Provincial Center for Disease Control and Prevention (CN), Mekelle University (ET), National Ilan University (TW), Lanzhou University (CN)
Openalex Percentile: Top 22%
interferon and immune responses
0.80
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