Impaired lipid metabolism by age-dependent DNA methylation alterations accelerates aging.

Autor: Xin Li, Jiaqiang Wang, Leyun Wang, Guihai Feng, Gen Li, Meixin Yu, Yufei Li, Chao Liu, Xuewei Yuan, Guangxi Zang, Zhihuan Li, Ling Zhao, Hong Ouyang, Qingli Quan, Guangyu Wang, Zhang, Charlotte, Oulan Li, Junkai Xiang, Jian-Kang Zhu, Wei Li
Předmět:
Zdroj: Proceedings of the National Academy of Sciences of the United States of America; 2/25/2020, Vol. 117 Issue 8, p4328-4336, 9p
Abstrakt: Epigenetic alterations and metabolic dysfunction are two hallmarks of aging. However, the mechanism of how their interaction regulates aging, particularly in mammals, remains largely unknown. Here we show ELOVL fatty acid elongase 2 (Elovl2), a gene whose epigenetic alterations are most highly correlated with age prediction, contributes to aging by regulating lipid metabolism. Impaired Elovl2 function disturbs lipid synthesis with increased endoplasmic reticulum stress and mitochondrial dysfunction, leading to key accelerated aging phenotypes. Restoration of mitochondrial activity can rescue age-related macular degeneration (AMD) phenotypes induced by Elovl2 deficiency in human retinal pigmental epithelial (RPE) cells. We revealed an epigenetic-metabolism axis contributing to aging and potentially to antiaging therapy. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index