Unveiling lactylation: A novel frontier in the pathogenesis of diabetic nephropathy (Review)

Emerging insights into lactate‑mediated protein lactylation illuminate novel regulatory axes in the pathogenesis of diabetic nephropathy (DN). While histone lactylation has established epigenetic associations with metabolic memory, expanding proteomic evidence reveals dynamic lactylation landscapes across extracellular matrix components, inflammatory mediators and redox regulators in renal compartments. The present review systematically catalogues DN‑relevant histones and non‑histone substrates undergoing functional lactylation, while mechanistically dissecting how hyperglycemia‑fueled lactate flux drives DN through lactate‑mediated protein modification landscapes. The present review further delineates the progress of research on the potential regulatory mechanisms involved in DN and delve into the possible functions and related mechanisms. This mechanistic reappraisal establishes lactylation topology mapping as a prerequisite for developing precision modulation approaches in DN management.

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Publication Details

Journal
International Journal of Molecular Medicine
Published
2026-03-27
DOI
https://doi.org/10.3892/ijmm.2026.5814
Primary Topic
Advanced Glycation End Products research
Type
article
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article

Unveiling lactylation: A novel frontier in the pathogenesis of diabetic nephropathy (Review)

Youhua Xu, Dingkun Gui, Niansong Wang, Yuanyuan Xiao
International Journal of Molecular Medicine
Advanced Glycation End Products research
article

Unveiling lactylation: A novel frontier in the pathogenesis of diabetic nephropathy (Review)

Youhua Xu, Dingkun Gui, Niansong Wang, Yuanyuan Xiao
article en

Abstract

Emerging insights into lactate‑mediated protein lactylation illuminate novel regulatory axes in the pathogenesis of diabetic nephropathy (DN). While histone lactylation has established epigenetic associations with metabolic memory, expanding proteomic evidence reveals dynamic lactylation landscapes across extracellular matrix components, inflammatory mediators and redox regulators in renal compartments. The present review systematically catalogues DN‑relevant histones and non‑histone substrates undergoing functional lactylation, while mechanistically dissecting how hyperglycemia‑fueled lactate flux drives DN through lactate‑mediated protein modification landscapes. The present review further delineates the progress of research on the potential regulatory mechanisms involved in DN and delve into the possible functions and related mechanisms. This mechanistic reappraisal establishes lactylation topology mapping as a prerequisite for developing precision modulation approaches in DN management.

International Journal of Molecular MedicineVol. 57(6)
Macau University of Science and Technology (MO), University of Macau (MO), Shanghai Sixth People's Hospital (CN)
Zero hunger
Openalex Percentile: Top 3%
Advanced Glycation End Products research
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