Chongqing Key Laboratory of Medicinal Chemistry & Molecular Pharmacology, Chongqing University of Technology, Chongqing, People's Republic of China.
Chongqing Key Laboratory of Medicinal Chemistry & Molecular Pharmacology, Chongqing University of Technology, Chongqing, People's Republic of China; College of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing, People's Republic of China.
J Nutr Biochem. 2023 Mar;113:109249. doi: 10.1016/j.jnutbio.2022.109249. Epub 2022 Dec 8.
Low-grade chronic inflammation originating from the adipose tissue and imbalance of lipid metabolism in the liver are the main drivers of the development of obesity and its related metabolic disorders. In this work, we found that garlic-derived exosomes (GDE) supplementation improved insulin resistance, altered the levels of inflammatory cytokines in serum and epididymal white adipose tissue (eWAT) by decreasing the accumulation of macrophages in HFD-fed mice. Meanwhile, we also observed that GDE regulated the expression of 6-phosphofructo-2-kinase/fructose-2, 6-biphosphatase 3 (PFKFB3), one of the critical glycolytic enzymes, to shape the metabolic reprograming of macrophage induced by lipopolysaccharide (LPS) and mitigate the inflammatory response in adipocytes via macrophage-adipocyte cross-talk. Data from small RNA sequencing, bioinformatical analysis and the gene over-expression revealed that miR-396e, one of the most abundant miRNAs of GDE, played a critical role in promoting the metabolic reprogramming of macrophage by directly targeting PFKFB3. The findings of this study not only provide an in-depth understanding of GDE protecting against inflammation in obesity but supply evidence to study the molecular mechanisms associated with the interspecies communication.
低水平的慢性炎症源于脂肪组织,肝脏的脂质代谢失衡,是肥胖及其相关代谢紊乱发展的主要驱动因素。在这项工作中,我们发现大蒜衍生的外泌体(GDE)补充剂通过减少高脂肪饮食喂养的小鼠中巨噬细胞的积累,改善了胰岛素抵抗,改变了血清和附睾白色脂肪组织(eWAT)中炎症细胞因子的水平。同时,我们还观察到 GDE 调节了 6-磷酸果糖-2-激酶/果糖-2,6-二磷酸酶 3(PFKFB3)的表达,PFKFB3 是一种关键的糖酵解酶,通过脂多糖(LPS)诱导的巨噬细胞代谢重编程,减轻脂肪细胞的炎症反应,通过巨噬细胞-脂肪细胞的串扰。来自小 RNA 测序、生物信息学分析和基因过表达的数据表明,GDE 中最丰富的 miRNA 之一 miR-396e 通过直接靶向 PFKFB3,在促进巨噬细胞的代谢重编程中发挥关键作用。这项研究的结果不仅深入了解了 GDE 对肥胖炎症的保护作用,还为研究与种间通讯相关的分子机制提供了证据。