Augmentation of scleral glycolysis promotes myopia through histone lactylation

IF 27.7 1区 生物学 Q1 CELL BIOLOGY
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, Hanyu Deng, Shengcong Liu, Xingxing Yang, Jia Qu, Wei Chen, Xiangtian Zhou, Fei Zhao
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Abstract

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.

Abstract Image

通过组蛋白乳酰化增强巩膜糖酵解促进近视的形成
近视的特点是巩膜成纤维细胞向肌成纤维细胞转分化(FMT)的不适应性增加。巩膜缺氧是导致近视的一个重要因素,但人们对缺氧如何诱发近视却知之甚少。在这里,我们发现小鼠和豚鼠的近视与缺氧诱导的巩膜中关键糖酵解酶表达和乳酸水平的增加有关。促进巩膜糖酵解或乳酸盐生成可诱导FMT和近视;相反,抑制糖酵解或乳酸盐生成则可消除或抑制FMT和近视。从机理上讲,巩膜糖酵解-乳酸盐水平的增加通过H3K18la促进了FMT和近视的发生,而这又促进了Notch1的表达。遗传分析发现,两个编码糖酵解酶的基因ENO2和TPI1显著富集。此外,增加豚鼠的糖摄入量不仅能诱导近视,还能通过巩膜糖酵解-乳酸-组蛋白乳酰化途径增强对近视诱导的反应。总之,我们认为巩膜糖酵解通过乳酸盐诱导的组蛋白乳酰化促进 FMT,从而导致近视。
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来源期刊
Cell metabolism
Cell metabolism 生物-内分泌学与代谢
CiteScore
48.60
自引率
1.40%
发文量
173
审稿时长
2.5 months
期刊介绍: Cell Metabolism is a top research journal established in 2005 that focuses on publishing original and impactful papers in the field of metabolic research.It covers a wide range of topics including diabetes, obesity, cardiovascular biology, aging and stress responses, circadian biology, and many others. Cell Metabolism aims to contribute to the advancement of metabolic research by providing a platform for the publication and dissemination of high-quality research and thought-provoking articles.
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