缺氧诱导组蛋白乳酸化促进肺动脉高压患者肺动脉平滑肌细胞增殖。

IF 3.5 2区 生物学 Q3 CELL BIOLOGY
Ai Chen, Zhihai Chen, Bangbang Huang, Guili Lian, Li Luo, Liangdi Xie
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引用次数: 0

摘要

肺动脉高压(Pulmonary hypertension, PH)以肺血管重构和肺动脉平滑肌细胞(PASMCs)过度增殖为特征。糖酵解在PH发病机制中起着至关重要的作用,但糖酵解与PASMCs增殖之间的表观遗传机制尚不清楚。组蛋白乳酸化是一种源于糖酵解乳酸的新型翻译后修饰,可能调节PASMCs的增殖。在缺氧条件下培养原代大鼠PASMCs,并用l -乳酸钠(NaLa)处理,以评估糖酵解活性和组蛋白乳酸化。RNA测序、RT-qPCR和Western blotting鉴定差异表达基因(DEGs),而ChIP-qPCR评估基因启动子处组蛋白乳酸化富集。在体内,采用缺氧诱导的PH大鼠模型来研究草酸酯对糖酵解的抑制作用。孟德尔随机化(MR)分析评估了胎盘生长因子(PGF)和ph之间的因果关系。缺氧和NaLa治疗显著增加糖酵解活性、乳酸生成和组蛋白乳酸化,促进PASMCs增殖。转录组学分析鉴定出157个基因,其中5个关键基因(Gbe1、Pgf、Mt2A、Ythdf2和Gys1)在组蛋白乳酸化反应中上调。ChIP-qPCR证实H3K18la在它们的启动子上富集。在缺氧PH大鼠中,用草酸酯抑制糖酵解可有效降低组蛋白乳酸化、PASMCs增殖和血管重构。MR分析确定PGF是导致PH风险的原因因素,提示潜在的治疗靶点。本研究揭示糖酵解诱导的组蛋白乳酸化可驱动ph下PASMCs增殖和血管重构。以乳酸代谢和组蛋白乳酸化为靶点可能提供一种新的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hypoxia-induced histone lactylation promotes pulmonary arterial smooth muscle cells proliferation in pulmonary hypertension.

Pulmonary hypertension (PH) is characterized by pulmonary vascular remodeling and excessive proliferation of pulmonary artery smooth muscle cells (PASMCs). Glycolysis plays a crucial role in PH pathogenesis, but the epigenetic mechanisms linking glycolysis to PASMCs proliferation remain unclear. Histone lactylation, a novel post-translational modification derived from glycolytic lactate, may regulate PASMCs proliferation. Primary rat PASMCs were cultured under hypoxia and treated with sodium L-lactate (NaLa) to assess glycolytic activity and histone lactylation. RNA sequencing, RT-qPCR, and Western blotting identified differentially expressed genes (DEGs), while ChIP-qPCR evaluated histone lactylation enrichment at gene promoters. In vivo, a hypoxia-induced PH rat model was used to examine the effect of glycolysis inhibition using oxamate. Mendelian randomization (MR) analysis assessed the causal relationship between placental growth factor (PGF) and PH. Hypoxia and NaLa treatment significantly increased glycolytic activity, lactate production, and histone lactylation, promoting PASMCs proliferation. Transcriptomic analysis identified 157 DEGs, with five key genes (Gbe1, Pgf, Mt2A, Ythdf2 and Gys1) upregulated in response to histone lactylation. ChIP-qPCR confirmed H3K18la enrichment at their promoters. Glycolysis inhibition with oxamate effectively reduced histone lactylation, PASMCs proliferation, and vascular remodeling in hypoxic PH rats. MR analysis identified PGF as a causal factor contributing to PH risk, suggesting a potential therapeutic target. This study reveals that glycolysis-induced histone lactylation drives PASMCs proliferation and vascular remodeling in PH. Targeting lactate metabolism and histone lactylation may provide a novel therapeutic approach.

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来源期刊
Molecular and Cellular Biochemistry
Molecular and Cellular Biochemistry 生物-细胞生物学
CiteScore
8.30
自引率
2.30%
发文量
293
审稿时长
1.7 months
期刊介绍: Molecular and Cellular Biochemistry: An International Journal for Chemical Biology in Health and Disease publishes original research papers and short communications in all areas of the biochemical sciences, emphasizing novel findings relevant to the biochemical basis of cellular function and disease processes, as well as the mechanics of action of hormones and chemical agents. Coverage includes membrane transport, receptor mechanism, immune response, secretory processes, and cytoskeletal function, as well as biochemical structure-function relationships in the cell. In addition to the reports of original research, the journal publishes state of the art reviews. Specific subjects covered by Molecular and Cellular Biochemistry include cellular metabolism, cellular pathophysiology, enzymology, ion transport, lipid biochemistry, membrane biochemistry, molecular biology, nuclear structure and function, and protein chemistry.
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