Tual-Chalot Simon, Gagnadoux Frédéric, Trzepizur Wojciech, Priou Pascaline, Andriantsitohaina Ramaroson, Martinez M Carmen
LUNAM Université, Angers, France; INSERM U1063, Angers, France.
LUNAM Université, Angers, France; INSERM U1063, Angers, France; Département de Pneumologie, CHU d'Angers, France.
Biochim Biophys Acta. 2014 Feb;1842(2):202-7. doi: 10.1016/j.bbadis.2013.11.017. Epub 2013 Nov 22.
Microparticles are deemed true biomarkers and vectors of biological information between cells. Depending on their origin, the composition of microparticles varies and the subsequent message transported by them, such as proteins, mRNA, or miRNA, can differ. In obstructive sleep apnea syndrome (OSAS), circulating microparticles are associated with endothelial dysfunction by reducing endothelial-derived nitric oxide production. Here, we have analyzed the potential role of circulating microparticles from OSAS patients on the regulation of angiogenesis and the involved pathway. VEGF content carried by circulating microparticles from OSAS patients was increased when compared with microparticles from non-OSAS patients. Circulating microparticles from OSAS patients induced an increase of angiogenesis that was abolished in the presence of the antagonist of endothelin-1 receptor type B. In addition, endothelin-1 secretion was increased in human endothelial cells treated by OSAS microparticles. We highlight that circulating microparticles from OSAS patients can modify the secretome of endothelial cells leading to angiogenesis.
微粒被认为是真正的生物标志物以及细胞间生物信息的载体。根据其来源不同,微粒的组成各异,其携带的后续信息(如蛋白质、mRNA或miRNA)也会有所不同。在阻塞性睡眠呼吸暂停综合征(OSAS)中,循环微粒通过减少内皮源性一氧化氮的产生与内皮功能障碍相关。在此,我们分析了OSAS患者循环微粒在血管生成调节及相关途径中的潜在作用。与非OSAS患者的微粒相比,OSAS患者循环微粒携带的VEGF含量增加。OSAS患者的循环微粒诱导血管生成增加,而在内皮素-1 B型受体拮抗剂存在的情况下这种增加被消除。此外,用OSAS微粒处理的人内皮细胞中内皮素-1的分泌增加。我们强调,OSAS患者的循环微粒可改变内皮细胞的分泌组,从而导致血管生成。