Targeting Endothelial KDM5A to Attenuate Aging and Ameliorate Age‐Associated Metabolic Abnormalities

Vascular aging accelerates the gradual deterioration of systemic organ function, yet its key driving factors are still largely unexplored. Here, it is demonstrated that lysine-specific demethylase 5A (KDM5A) decreases and histone H3 lysine 4 (H3K4me3) increases in vascular endothelial cells (VECs) isolated from ageing mice and VEC senescence models. KDM5A deficiency exacerbated endothelial cell aging in vitro. Endothelial-specific KDM5A-deficient mice exhibit shortened lifespan and multiple senescent phenotypes, including fat accumulation, reduced thermogenic capacity, skeletal kyphosis, and age-related liver lesions, while maintaining VECs-specific KDM5A levels attenuates these adverse metabolic abnormalities and prolongs lifespan. Mechanistically, endothelial KDM5A deficiency aggravates aging-associated fatty acid (FA) metabolism disorders by enhancing H3K4me3 enrichment at the promoter region of FA-binding protein 4 (FABP4), which leads to active FABP4 transcription. Together, the study reveals the regulatory mechanisms of KDM5A in age-dependent metabolic disorders and identifies KDM5A/FABP4 axis as a potential therapeutic target for vascular aging and related organ dysfunction.

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Publication Details

Journal
Advanced Science
Published
2025-11-14
DOI
https://doi.org/10.1002/advs.202512657
Primary Topic
Epigenetics and DNA Methylation
Type
article
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article

Targeting Endothelial KDM5A to Attenuate Aging and Ameliorate Age‐Associated Metabolic Abnormalities

Lifeng Liang, Xi Sun, Yan Zhou, J. Qi et al.
Advanced Science
Epigenetics and DNA Methylation
article

Targeting Endothelial KDM5A to Attenuate Aging and Ameliorate Age‐Associated Metabolic Abnormalities

Lifeng Liang, Xi Sun, Yan Zhou, J. Qi, Jiaran Shi, Juntao Chen, Xiaoxin Zhang, Kun Yang, Cuicui Lyu, Rifeng Gao, Yang Lyu, Aiqiang Dong, Weijun Yang, Wei Wei, Bo Li, Chao Chen, Wenli Li, Ling Yang, Jiahui Cheng, Xian Zhu, Yizhe Zhang, Xiaoting Xu
article en

Abstract

Vascular aging accelerates the gradual deterioration of systemic organ function, yet its key driving factors are still largely unexplored. Here, it is demonstrated that lysine-specific demethylase 5A (KDM5A) decreases and histone H3 lysine 4 (H3K4me3) increases in vascular endothelial cells (VECs) isolated from ageing mice and VEC senescence models. KDM5A deficiency exacerbated endothelial cell aging in vitro. Endothelial-specific KDM5A-deficient mice exhibit shortened lifespan and multiple senescent phenotypes, including fat accumulation, reduced thermogenic capacity, skeletal kyphosis, and age-related liver lesions, while maintaining VECs-specific KDM5A levels attenuates these adverse metabolic abnormalities and prolongs lifespan. Mechanistically, endothelial KDM5A deficiency aggravates aging-associated fatty acid (FA) metabolism disorders by enhancing H3K4me3 enrichment at the promoter region of FA-binding protein 4 (FABP4), which leads to active FABP4 transcription. Together, the study reveals the regulatory mechanisms of KDM5A in age-dependent metabolic disorders and identifies KDM5A/FABP4 axis as a potential therapeutic target for vascular aging and related organ dysfunction.

Advanced ScienceVol. 13(6)
Zhejiang Chinese Medical University (CN), Shanghai Jiao Tong University (CN), Fudan University (CN), Renji Hospital (CN), Shanghai Chest Hospital (CN), Ningbo Medical Center Lihuili Hospital (CN), Zhongshan Hospital (CN), Obstetrics and Gynecology Hospital of Fudan University (CN), Beijing Friendship Hospital (CN), Second Affiliated Hospital of Zhejiang University (CN)
Openalex Percentile: Top 69%
Epigenetics and DNA Methylation
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