Department of Pharmacology and Toxicology, University of Mississippi Medical Center, Jackson, Mississippi, USA.
J Cell Physiol. 2021 Nov;236(11):7578-7590. doi: 10.1002/jcp.30401. Epub 2021 Apr 30.
Endothelial glycolytic metabolism plays an important role in the process of angiogenesis. TP53-induced glycolysis and apoptosis regulator (TIGAR) is a significant mediator of cellular energy homeostasis. However, the role of TIGAR in endothelial metabolism, angiogenesis, and coronary flow reserve (CFR) has not been studied. The present study investigated whether knockout (KO) of TIGAR improves endothelial glycolytic function and angiogenesis. In vitro, aortic endothelial cells (ECs) from TIGAR KO mice exhibited increased expression of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase isoform-3 (PFKFB3) and increased glycolytic function. These were accompanied by increased mitochondrial basal/maximal respiration and ATP production. Furthermore, knockout of TIGAR in ECs enhanced endothelial proliferation, migration, and tube formation. Knockout of TIGAR also significantly increased aortic sprouting ex vivo. In vivo, knockout of TIGAR increased the expression of proangiogenic factor, angiopoietin-1 (Ang-1) in mouse hearts. Knockout of TIGAR also significantly increased coronary capillary density with enhanced CFR in these hearts. Furthermore, TIGAR KO mice subjected to pressure overload (PO), a common model to study angiogenesis and cardiac hypertrophy, exhibited elevated expression of Ang-1, VEGF, and PFKFB3 than that of the wild-type (WT) mice. WT mice subjected to PO exhibited a significant reduction of coronary capillary density and impaired CFR, but TIGAR KO mice did not. In addition, knockout of TIGAR blunted TAC-induced cardiac hypertrophy and dysfunction seen in the WT mice. In conclusion, knockout of TIGAR improves endothelial angiogenetic capabilities by enhancing the endothelial glycolytic function, mitochondrial respiration, and proangiogenic signaling, which leads to increased coronary capillary density and vascular function and protects against chronic stress.
内皮细胞糖酵解代谢在血管生成过程中发挥着重要作用。TP53 诱导的糖酵解和凋亡调节剂(TIGAR)是细胞能量平衡的重要介质。然而,TIGAR 在血管内皮代谢、血管生成和冠状动脉血流储备(CFR)中的作用尚未得到研究。本研究旨在探讨 TIGAR 敲除(KO)是否能改善内皮细胞的糖酵解功能和血管生成。在体外,TIGAR KO 小鼠的主动脉内皮细胞(ECs)表现出 6-磷酸果糖-2-激酶/果糖-2,6-双磷酸酶同工酶-3(PFKFB3)表达增加和糖酵解功能增强。这伴随着线粒体基础/最大呼吸和 ATP 产生的增加。此外,ECs 中 TIGAR 的敲除增强了内皮细胞的增殖、迁移和管状结构形成。TIGAR 的敲除还显著增加了主动脉在体外的发芽。在体内,TIGAR 的敲除增加了小鼠心脏中促血管生成因子血管生成素-1(Ang-1)的表达。TIGAR 的敲除还显著增加了这些心脏中的冠状动脉毛细血管密度,并增强了 CFR。此外,TIGAR KO 小鼠在压力超负荷(PO)后,即研究血管生成和心脏肥大的常用模型,表现出 Ang-1、VEGF 和 PFKFB3 的表达升高,高于野生型(WT)小鼠。PO 后 WT 小鼠的冠状动脉毛细血管密度显著减少,CFR 受损,但 TIGAR KO 小鼠没有。此外,TIGAR 的敲除减轻了 WT 小鼠 TAC 诱导的心脏肥大和功能障碍。总之,TIGAR 的敲除通过增强内皮细胞的糖酵解功能、线粒体呼吸和促血管生成信号,改善内皮细胞的血管生成能力,增加冠状动脉毛细血管密度和血管功能,保护其免受慢性应激的影响。