Metabolomics Core Laboratory, Healthy Aging Research Center, Chang Gung University, Taoyuan City 33302, Taiwan.
Clinical Metabolomics Core Laboratory, Chang Gung Memorial Hospital, Taoyuan City 33305, Taiwan.
Cells. 2021 Dec 20;10(12):3597. doi: 10.3390/cells10123597.
7-Ketocholesterol (7KCh) is a major oxidized cholesterol product abundant in lipoprotein deposits and atherosclerotic plaques. Our previous study has shown that 7KCh accumulates in erythrocytes of heart failure patients, and further investigation centered on how 7KCh may affect metabolism in cardiomyocytes. We applied metabolomics to study the metabolic changes in cardiac cell line HL-1 after treatment with 7KCh. Mevalonic acid (MVA) pathway-derived metabolites, such as farnesyl-pyrophosphate and geranylgeranyl-pyrophosphate, phospholipids, and triacylglycerols levels significantly declined, while the levels of lysophospholipids, such as lysophosphatidylcholines (lysoPCs) and lysophosphatidylethanolamines (lysoPEs), considerably increased in 7KCh-treated cells. Furthermore, the cholesterol content showed no significant change, but the production of cholesteryl esters was enhanced in the treated cells. To explore the possible mechanisms, we applied mRNA-sequencing (mRNA-seq) to study genes differentially expressed in 7KCh-treated cells. The transcriptomic analysis revealed that genes involved in lipid metabolic processes, including MVA biosynthesis and cholesterol transport and esterification, were differentially expressed in treated cells. Integrated analysis of both metabolomic and transcriptomic data suggests that 7KCh induces cholesteryl ester accumulation and reprogramming of lipid metabolism through altered transcription of such genes as sterol O-acyltransferase- and phospholipase A2-encoding genes. The 7KCh-induced reprogramming of lipid metabolism in cardiac cells may be implicated in the pathogenesis of cardiovascular diseases.
7-酮胆固醇(7KCh)是一种富含脂蛋白沉积物和动脉粥样硬化斑块的主要胆固醇氧化产物。我们之前的研究表明,7KCh 在心力衰竭患者的红细胞中积累,进一步的研究集中在 7KCh 如何影响心肌细胞的代谢。我们应用代谢组学研究了 7KCh 处理后的 HL-1 心脏细胞系的代谢变化。甲羟戊酸(MVA)途径衍生的代谢物,如法呢基焦磷酸和香叶基焦磷酸、磷脂和三酰基甘油水平显著下降,而溶血磷脂,如溶血磷脂酰胆碱(lysoPC)和溶血磷脂酰乙醇胺(lysoPE)的水平在 7KCh 处理的细胞中显著增加。此外,胆固醇含量没有明显变化,但处理细胞中的胆固醇酯生成增强。为了探讨可能的机制,我们应用 mRNA 测序(mRNA-seq)研究了 7KCh 处理细胞中差异表达的基因。转录组分析表明,参与脂质代谢过程的基因,包括 MVA 生物合成和胆固醇转运和酯化,在处理细胞中差异表达。代谢组学和转录组学数据的综合分析表明,7KCh 通过固醇 O-酰基转移酶和磷脂酶 A2 编码基因等基因的转录改变,诱导胆固醇酯的积累和脂质代谢的重编程。7KCh 诱导的心脏细胞脂质代谢重编程可能与心血管疾病的发病机制有关。