An oxidized ribonucleotide 8-oxoGTP drives neuroinflammation and accelerates cognitive decline

Oxidative stress is a hallmark of aging and a key driver of neurodegenerative diseases. While much attention has been given to oxidative damage of macromolecules, the functional consequences of oxidizing the abundant nucleotide triphosphate (NTP) pool remain largely unknown. Here, we identify oxidized GTP (8-oxoGTP)-a major product of NTP oxidation-not as a mere marker of damage, but as an endogenous signaling molecule that drives microglial activation and neuroinflammation. 8-oxoGTP accumulated in the aging mouse brain, and its elevation was sufficient to induce synaptic dysfunction, tau hyperphosphorylation, neuronal loss, and cognitive decline. Mechanistically, 8-oxoGTP functioned as a potent activator of heterotrimeric G proteins, binding more strongly to Gα subunits than GTP itself, triggering Src kinase/MAPK/Akt/NF-κB signaling in microglia, leading to pro-inflammatory cytokine production, reactive oxygen species generation, and neurotoxicity. Pharmacological inhibition of Src family kinases rescued the neuroinflammatory and cognitive phenotypes induced by 8-oxoGTP. Our findings reveal a previously unrecognized mechanism linking nucleotide oxidation to age-associated neurodegenerative processes.

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Journal
Science Advances
Published
2026-10-28
DOI
https://doi.org/10.1126/sciadv.aee0110
Primary Topic
Neuroinflammation and Neurodegeneration Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

An oxidized ribonucleotide 8-oxoGTP drives neuroinflammation and accelerates cognitive decline

Ruomei Qi, Liqun Zhang, Yaqing Ma, Zheli Jiang et al.
1 links
Science Advances
Neuroinflammation and Neurodegeneration Mechanisms
article

An oxidized ribonucleotide 8-oxoGTP drives neuroinflammation and accelerates cognitive decline

Ruomei Qi, Liqun Zhang, Yaqing Ma, Zheli Jiang, Jian‐Ping Cai, Da‐Peng Dai, Jin Li, Lv-Tao Zeng, Ju Cui, Wei Zhang, HU Guo-xin, Xiaoyang Zhou, Zhenhe Wang, Zihui Wang, Xu-Fan Gao, Gang Sheng, Ran Huan, Rui Li, Jia-Xin Pan, Zheng-Lu Wang, Wen Su, Hai-Bo Chen, Ting Wang
article en

Abstract

Oxidative stress is a hallmark of aging and a key driver of neurodegenerative diseases. While much attention has been given to oxidative damage of macromolecules, the functional consequences of oxidizing the abundant nucleotide triphosphate (NTP) pool remain largely unknown. Here, we identify oxidized GTP (8-oxoGTP)-a major product of NTP oxidation-not as a mere marker of damage, but as an endogenous signaling molecule that drives microglial activation and neuroinflammation. 8-oxoGTP accumulated in the aging mouse brain, and its elevation was sufficient to induce synaptic dysfunction, tau hyperphosphorylation, neuronal loss, and cognitive decline. Mechanistically, 8-oxoGTP functioned as a potent activator of heterotrimeric G proteins, binding more strongly to Gα subunits than GTP itself, triggering Src kinase/MAPK/Akt/NF-κB signaling in microglia, leading to pro-inflammatory cytokine production, reactive oxygen species generation, and neurotoxicity. Pharmacological inhibition of Src family kinases rescued the neuroinflammatory and cognitive phenotypes induced by 8-oxoGTP. Our findings reveal a previously unrecognized mechanism linking nucleotide oxidation to age-associated neurodegenerative processes.

Science AdvancesVol. 12(44)
Capital Medical University (CN), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Wenzhou Medical University (CN), First Affiliated Hospital of Wenzhou Medical University (CN), Shandong Provincial Hospital (CN), Beijing Hospital (CN), Peking University Shougang Hospital (CN), Shandong First Medical University (CN)
National Natural Science Foundation of China
Good health and well-being
Openalex Percentile: Top 18%
Neuroinflammation and Neurodegeneration Mechanisms
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