巨噬细胞极化
转录组
代谢组学
巨噬细胞
动脉硬化
医学
生物
生物信息学
计算生物学
基因
内科学
遗传学
基因表达
体外
作者
Lin Shen,Han Li,Weiqian Chen,Yanping Su,Junchao Yu,Minjiang Chen,Gaofeng Shu,Enqi Qiao,Xiaoju Guo,Min Xu,Shuiwei Xia,Zhao Zhi,Chenying Lu,Jiansong Ji
标识
DOI:10.1016/j.bbadis.2022.166550
摘要
The polarization of macrophages often leads to severe calcification and necrosis in aged atherosclerotic plaques, which eventually leads to poor prognosis of ischaemic cardiovascular and cerebrovascular diseases. More reliable diagnostic methods are urgently needed to discover therapeutic targets of macrophage polarization in aged atherosclerotic plaques. Metabolomics of aged plaques (n = 20) and macrophage polarization transcriptomes (n = 30) were integrated to identify metabolic therapeutic targets of macrophage polarization associated with aged plaque. Finally, metabolic inhibitors were used to verify the reliability of the target genes. Integrated multiomics analysis revealed that 6 metabolic pathways (including 21 genes) regulate macrophage polarization in aged atherosclerosis. Targeted treatment of macrophage polarization with metabolic inhibitors can effectively reduce the adverse risk of aged atherosclerosis. The combination of transcriptomics and metabolomics approaches can identify effective therapeutic targets for macrophage polarization in arteriosclerosis.
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