Codagnone Marilina, Recchiuti Antonio, Lanuti Paola, Pierdomenico Anna Maria, Cianci Eleonora, Patruno Sara, Mari Veronica Cecilia, Simiele Felice, Di Tomo Pamela, Pandolfi Assunta, Romano Mario
Department of Medical, Oral, and Biotechnological Sciences, G. D'Annunzio University of Chieti-Pescara, Chieti, Italy.
Center on Aging Science and Translational Medicine (CeSI-MeT), G. D'Annunzio University of Chieti-Pescara, Chieti, Italy; and.
FASEB J. 2017 May;31(5):1856-1866. doi: 10.1096/fj.201600952R. Epub 2017 Jan 18.
The proresolution lipid mediator lipoxin (LX)A bestows protective bioactions on endothelial cells. We examined the impact of LXA on transcellular endothelial signaling microRNA (miR)-containing microvesicles. We report LXA inhibition of MV release by TNF-α-treated HUVECs, associated with the down-regulation of 18 miR in endothelial microvesicles (EMVs) and the up-regulation of miR-126-5p, both in HUVECs and in EMVs. LXA up-regulated miR-126-5p by ∼5-fold in HUVECs and promoted a release of microvesicles (LXA-EMVs) that enhanced miR-126-5p by ∼7-fold in recipient HUVECs. In these cells, LXA-EMVs abrogated the up-regulation of VCAM-1, induced in recipient HUVECs by EMVs released by untreated or TNF-α-treated HUVECs. LXA-EMVs also reduced by ∼40% the expression of SPRED1, which we validated as an miR-126-5p target, whereas they stimulated monolayer repair in an wound assay. This effect was lost when the EMVs were depleted of miR-126-5p. These results provide evidence that changes in miR expression and microvesicle packaging and transfer represent a mechanism of action of LXA, which may be relevant in vascular biology and inflammation.-Codagnone, M., Recchiuti, A., Lanuti, P., Pierdomenico, A. M., Cianci, E., Patruno, S., Mari, V. C., Simiele, F., Di Tomo, P., Pandolfi, A., Romano, M. Lipoxin A stimulates endothelial miR-126-5p expression and its transfer microvesicles.
促消退脂质介质脂氧素(LX)A赋予内皮细胞保护性生物活性。我们研究了LX对含跨细胞内皮信号微小RNA(miR)的微泡的影响。我们报告了LX对经肿瘤坏死因子-α(TNF-α)处理的人脐静脉内皮细胞(HUVECs)释放微泡的抑制作用,这与内皮微泡(EMVs)中18种miR的下调以及HUVECs和EMVs中miR-126-5p的上调有关。LX使HUVECs中的miR-126-5p上调约5倍,并促进微泡(LXA-EMVs)的释放,使受体HUVECs中的miR-126-5p增强约7倍。在这些细胞中,LXA-EMVs消除了未经处理或经TNF-α处理的HUVECs释放的EMVs在受体HUVECs中诱导的血管细胞黏附分子-1(VCAM-1)的上调。LXA-EMVs还使SPRED1的表达降低了约40%,我们验证了SPRED1是miR-126-5p的靶标,而它们在伤口试验中刺激了单层修复。当EMVs中缺乏miR-126-5p时,这种作用消失。这些结果证明,miR表达以及微泡包装和转移的变化代表了LX的一种作用机制,这可能与血管生物学和炎症相关。-科达尼奥内,M.,雷基乌蒂,A.,拉努蒂,P.,皮耶尔多梅尼科,A.M.,钱奇,E.,帕特鲁诺,S.,马里,V.C.,西米莱,F.,迪托莫,P.,潘多尔菲,A.,罗曼诺,M.脂氧素A刺激内皮miR-126-5p表达及其向微泡的转移