糖酵解
厌氧糖酵解
转分化
缺氧(环境)
组蛋白
巩膜
化学
细胞生物学
生物
内分泌学
内科学
生物化学
眼科
医学
新陈代谢
氧气
基因
有机化学
干细胞
作者
Xiaolei Lin,Yi Lei,Miaozhen Pan,Changxi Hu,Bintao Xie,Wenjing Wu,Jianzhong Su,Yating Li,Yuhan Tan,Xiaohuan Wei,Zhengbo Xue,Ruiyan Xu,Mengqi Di,Han‐Yu Deng,Shengcong Liu,Xingxing Yang,Jia Qu,Wei Chen,Xiangtian Zhou,Fei Zhao
出处
期刊:Cell Metabolism
[Elsevier]
日期:2024-01-16
卷期号:36 (3): 511-525.e7
被引量:8
标识
DOI:10.1016/j.cmet.2023.12.023
摘要
Myopia is characterized of maladaptive increases in scleral fibroblast-to-myofibroblast transdifferentiation (FMT). Scleral hypoxia is a significant factor contributing to myopia, but how hypoxia induces myopia is poorly understood. Here, we showed that myopia in mice and guinea pigs was associated with hypoxia-induced increases in key glycolytic enzymes expression and lactate levels in the sclera. Promotion of scleral glycolysis or lactate production induced FMT and myopia; conversely, suppression of glycolysis or lactate production eliminated or inhibited FMT and myopia. Mechanistically, increasing scleral glycolysis-lactate levels promoted FMT and myopia via H3K18la, and this promoted Notch1 expression. Genetic analyses identified a significant enrichment of two genes encoding glycolytic enzymes, ENO2 and TPI1. Moreover, increasing sugar intake in guinea pigs not only induced myopia but also enhanced the response to myopia induction via the scleral glycolysis-lactate-histone lactylation pathway. Collectively, we suggest that scleral glycolysis contributes to myopia by promoting FMT via lactate-induced histone lactylation.
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