Departamento de Ciencias Médicas Básicas, Instituto de Medicina Molecular Aplicada (IMMA) Nemesio Díez, Facultad de Medicina, Universidad San Pablo-CEU, CEU Universities, Urbanización Montepríncipe, 28660 Boadilla del Monte, Spain.
Centro de Metabolómica y Bioanálisis (CEMBIO), Facultad de Farmacia, Universidad San Pablo-CEU, CEU Universities, Urbanización Montepríncipe, 28660 Boadilla del Monte, Spain.
Int J Mol Sci. 2023 Aug 12;24(16):12714. doi: 10.3390/ijms241612714.
The resolution of inflammation is a complex process that is critical for removing inflammatory cells and restoring tissue function. The dysregulation of these mechanisms leads to chronic inflammatory disorders. Platelets, essential cells for preserving homeostasis, are thought to play a role in inflammation as they are a source of immunomodulatory factors. Our aim was to identify key metabolites carried by platelet-derived extracellular vesicles (PL-EVs) in a model of allergic inflammation. PL-EVs were isolated by serial ultracentrifugation using platelet-rich plasma samples obtained from platelet apheresis from severely ( = 6) and mildly ( = 6) allergic patients and non-allergic individuals used as controls ( = 8). PL-EVs were analysed by a multiplatform approach using liquid and gas chromatography coupled to mass spectrometry (LC-MS and GC-MS, respectively). PL-EVs obtained from severely and mildly allergic patients and control individuals presented comparable particle concentrations and sizes with similar protein concentrations. Strikingly, PL-EVs differed in their lipid and metabolic content according to the severity of inflammation. L-carnitine, ceramide (Cer (d18:0/24:0)), and several triglycerides, all of which seem to be involved in apoptosis and regulatory T functions, were higher in PL-EVs from patients with mild allergic inflammation than in those with severe inflammation. In contrast, PL-EVs obtained from patients with severe allergic inflammation showed an alteration in the arachidonic acid pathway. This study demonstrates that PL-EVs carry specific lipids and metabolites according to the degree of inflammation in allergic patients and propose novel perspectives for characterising the progression of allergic inflammation.
炎症的消退是一个复杂的过程,对于清除炎症细胞和恢复组织功能至关重要。这些机制的失调会导致慢性炎症性疾病。血小板是维持内环境稳定的重要细胞,被认为在炎症中发挥作用,因为它们是免疫调节因子的来源。我们的目的是鉴定过敏炎症模型中血小板衍生的细胞外囊泡(PL-EV)携带的关键代谢物。使用富含血小板的血浆样本通过连续超速离心从严重(n = 6)和轻度(n = 6)过敏患者以及作为对照的非过敏个体(n = 8)中分离 PL-EV。使用液质联用(LC-MS)和气质联用(GC-MS)的多平台方法分析 PL-EV。从严重和轻度过敏患者和对照个体中获得的 PL-EV 具有可比的颗粒浓度和大小,且蛋白浓度相似。引人注目的是,PL-EV 的脂质和代谢物含量根据炎症的严重程度而不同。L-肉碱、神经酰胺(Cer(d18:0/24:0))和几种甘油三酯,所有这些似乎都参与细胞凋亡和调节性 T 细胞功能,在轻度过敏炎症患者的 PL-EV 中含量高于严重炎症患者。相比之下,严重过敏炎症患者的 PL-EV 显示出花生四烯酸途径的改变。这项研究表明,PL-EV 根据过敏患者的炎症程度携带特定的脂质和代谢物,并为表征过敏炎症的进展提出了新的观点。