Lactate promotes endothelial-to-mesenchymal transition via Snail1 lactylation after myocardial infarction

• Published in: Science advances Vol. 9; no. 5; p. eadc9465
• Main Authors: Fan, Min, Yang, Kun, Wang, Xiaohui, Chen, Linjian, Gill, P Spencer, Ha, Tuanzhu, Liu, Li, Lewis, Nicole H, Williams, David L, Li, Chuanfu
• Format: Journal Article
• Language: English
• Published: United States American Association for the Advancement of Science 03.02.2023
• Subjects: Biomedicine and Life Sciences; Cell Biology; Endothelial Cells - metabolism; Fibrosis; Humans; Hypoxia - metabolism; Lactic Acid; Myocardial Infarction - metabolism; SciAdv r-articles; Signal Transduction; Transforming Growth Factor beta - metabolism
• ISSN: 2375-2548; 2375-2548
• DOI: 10.1126/sciadv.adc9465

High levels of lactate are positively associated with the prognosis and mortality in patients with heart attack. Endothelial-to-mesenchymal transition (EndoMT) plays an important role in cardiac fibrosis. Here, we report that lactate exerts a previously unknown function that increases cardiac fibrosis and exacerbates cardiac dysfunction by promoting EndoMT following myocardial infarction (MI). Treatment of endothelial cells with lactate disrupts endothelial cell function and induces mesenchymal-like function following hypoxia by activating the TGF-β/Smad2 pathway. Mechanistically, lactate induces an association between CBP/p300 and Snail1, leading to lactylation of Snail1, a TGF-β transcription factor, through lactate transporter monocarboxylate transporter (MCT)-dependent signaling. Inhibiting Snail1 diminishes lactate-induced EndoMT and TGF-β/Smad2 activation after hypoxia/MI. The MCT inhibitor CHC mitigates lactate-induced EndoMT and Snail1 lactylation. Silence of MCT1 compromises lactate-promoted cardiac dysfunction and EndoMT after MI. We conclude that lactate acts as an important molecule that up-regulates cardiac EndoMT after MI via induction of Snail1 lactylation.