The DOI matches its Crossref record; 66 of the 66 references it cites were found in a registry or an index.
Protein lactylation induced by neural excitation
Open accessPublished version of a preprint
Abstract
Abstract Lactate is known to have diverse roles in the brain at the molecular and behavioral levels under both physiological and pathophysiological conditions, such as learning and memory and regulation of mood. Recently, a novel post-translational modification called lysine lactylation has been found in histone H3 of mouse macrophages, and the lactylation levels paralleled the intracellular lactate levels 1 . However, it is unknown whether lysine lactylation occurs in brain cells, and if it does, whether lactylation is induced by the stimuli that accompany changes in lactate levels. Herein, we reveal that lysine lactylation in brain cells is regulated by systemic changes in lactate levels, neural excitation, and behaviorally relevant stimuli. Lysine lactylation levels were increased by lactate treatment and by high-potassium-induced depolarization in cultured primary neurons; these increases were attenuated by pharmacological inhibition of monocarboxylate transporter 2 and lactate dehydrogenase, respectively, suggesting that both cell-autonomous and non-cell-autonomous neuronal mechanisms are involved in overall lysine lactylation. In vivo , electroconvulsive stimulation increased lysine lactylation levels in the prefrontal cortices of mice, and its levels were positively correlated with the expression levels of the neuronal activity marker c-Fos on an individual cell basis. In the social defeat stress model of depression in which brain lactate levels increase, lactylation levels were increased in the prefrontal cortices of the defeated mice, which was accompanied by increased c-Fos expression, decreased social behaviors, and increased anxiety-like behaviors, suggesting that stress-induced neuronal excitation may induce lysine lactylation, thereby affecting mood-related behaviors. Further, we identified 63 candidate lysine-lactylated proteins in the mouse cortex and found that lactylation levels in histone H1 increased in response to defeat stress. This study may open up an avenue for exploration of a novel role of neuronal activity-induced lactate mediated by protein lactylation in the brain.
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“Recent findings indicate that lactate-associated lactylation modulates glial inflammatory states and neuronal synaptic function, supporting its role in neuroplasticity (Yao et al., 2023; Hagihara et al., 2021).”
From Histone modifications and depression: epigenetic mechanisms, therapeutic targets, and translational outlook (2026) · cites this paper as Hagihara et al., 2021
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Research works printed but not linked: 1
- Hagihara, 2021, Systematic analysis of brain lactate and pH levels in 65 animal models related to neuropsychiatric conditions, bioRxiv
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Lactate metabolism in human health and disease
Li, X., Yang, Y., Zhang, B., Lin, X., Fu, X., An, Y., Zou, Y., Wang, J.-X., Wang, Z., & Yu, T. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-01151-3 · Cited by 1,454
Lactylation of METTL16 promotes cuproptosis via m6A-modification on FDX1 mRNA in gastric cancer
Sun, L., Zhang, Y., Yang, B., Sun, S., Zhang, P., Luo, Z., Feng, T., Cui, Z., Zhu, T., Li, Y., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-42025-8 · Cited by 542
Lactate and lactylation in cancer
Chen, J., Huang, Z., Chen, Y., Tian, H., Chai, P., Shen, Y., Yao, Y., Xu, S., Ge, S., & Jia, R. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-02082-x · Cited by 545
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Metadata
- Authors
- Hagihara, H., Shoji, H., Otabi, H., Toyoda, A., Katoh, K., Namihira, M., & Miyakawa, T.
- Affiliations
- Fujita Health University (JP)
- Ibaraki University (JP)
- Artificial Intelligence Research Center (JP)
- National Institute of Advanced Industrial Science and Technology (JP)
- Corresponding author
- Miyakawa, Tsuyoshi
- ORCID
- Venue
- Cell Reports
- Publisher
- Elsevier BV
- Published
- 2021-10
- Volume
- 37
- Issue
- 2
- Pages
- 109820
- ISSN
- 2211-1247 (ISSN-L)
- OpenAlex
- W3206354625
- Cited by
- 349
- References
- 66
- Citations by year
- 2026: 63 · 2025: 102 · 2024: 78 · 2023: 71 · 2022: 32 · 2021: 3
- FWCI
- 22.20
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Cell Reports (publishedVersion, cc-by-nc-nd)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
- SSRN Electronic Journal (acceptedVersion)
- PubMed (publishedVersion)
- Funders
- Japan Society for the Promotion of Science (JP16H06276, JP18K07378, JP19K06502, JP20H00522)
- Ministry of Education, Culture, Sports, Science and Technology (JP16H06462, JP17H06413, JP17H06417, JPMXP0618217663)
- Japan Agency for Medical Research and Development (JP18dm0107101, JP20he0622012h0001)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurobiology and Insect Physiology Research
- Keywords
- lysine lactylation, lactate, neuronal excitation, social stress, brain cells, c-fos, anxiety-like behavior, social behavior, histone H1, post-translational modification, neuronal activity
- MeSH terms
- Social Defeat, Action Potentials, Animals, Anxiety, Behavior, Animal, Brain, Cells, Cultured, Histones, Lysine, Mice, Inbred C57BL, Mice, Inbred ICR, Neurons, Protein Processing, Post-Translational, Proto-Oncogene Proteins c-fos, Lactic Acid, Proteome, Mice
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