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首页> 外文期刊>Journal of Extracellular Vesicles >In vitro decidualisation of human endometrial stromal cells is enhanced by seminal fluid extracellular vesicles
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In vitro decidualisation of human endometrial stromal cells is enhanced by seminal fluid extracellular vesicles

机译:精液细胞外囊泡增强人子宫内膜基质细胞的体外蜕膜

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摘要

ABSTRACT Extracellular vesicles are highly abundant in seminal fluids and have a known role enhancing sperm function. Clinical pregnancy rates after IVF treatment are improved after female exposure to seminal fluid. Seminal fluid extracellular vesicles (SF-EVs) are candidate enhancers, however, whether SF-EVs interact with cells from the endometrium and modulate the implantation processes is unknown. Here, we investigated whether SF-EVs interact with endometrial stromal cells (ESCs) and enhance decidualisation, a requisite for implantation. SF-EVs, isolated from human seminal fluid ( n =?11) by ultracentrifugation, were characterised by nanoparticle tracking analysis and Western blotting, and purified using size exclusion chromatography. Non-decidualised and decidualised primary ESCs ( n =?5) were then treated with SF-EVs. Binding of bio-maleimide-labelled SF-EVs was detected by flow cytometry and fluorescence microscopy. Prolactin and IGFBP-1 protein levels in culture media were also analysed after single and multiple SF-EV exposure. SF-EVs size ranged from 50 to 300?nm, and they expressed exosomal markers (ALIX, SYNTENIN-1, CD9 and CD81). SF-EVs bound to non-decidualised and decidualised ESCs at similar levels. ESCs prolactin secretion was increased after single ( p =?0.0044) and multiple ( p =?0.0021) SF-EV exposure. No differences were found in IGFBP-1 protein levels. In conclusion, SF-EVs enhance in vitro ESC decidualisation and increase secretion of prolactin, an essential hormone in implantation. This elucidates a novel role of SF-EVs on endometrial receptivity. Abbreviations: ECACC: European Collection of Authenticated Cell Cultures; ESCs: endometrial stromal cells; EVs: extracellular vesicles; FCS: foetal calf serum; HRP: horse-radish peroxidase; IFNγ: interferon-gamma; IGF: insulin-like growth factor; IGFBP-1: insulin-like growth factor binding protein 1; IVF: in vitro fertilisation; MVB: multivesicular bodies; NTA: nanoparticle tracking analysis; PRLR ~(?/?): homozygous prolactin receptor knockout; RT: room temperature; SF-EVs: seminal fluid extracellular vesicles; STR: short tandem repeat; TGFβ: transforming growth factor β; uNK: uterine natural killer
机译:摘要细胞外囊泡在精液中高度丰富,并且具有增强精子功能的已知作用。女性接触精液后,IVF治疗后的临床妊娠率得到改善。精液细胞外囊泡(SF-EVs)是候选增强剂,但是,SF-EVs是否与子宫内膜细胞相互作用并调节植入过程尚不清楚。在这里,我们调查了SF-EV是否与子宫内膜基质细胞(ESC)相互作用并增强蜕膜形成,这是植入的必要条件。通过超速离心从人精液中分离出的SF-EV(n =?11),通过纳米颗粒跟踪分析和Western印迹进行表征,并使用尺寸排阻色谱法进行纯化。然后用SF-EV对未蜕膜化和蜕膜化的原始ESC(n =?5)进行处理。通过流式细胞仪和荧光显微镜检测生物马来酰亚胺标记的SF-EV的结合。一次和多次SF-EV暴露后,还分析了培养基中的催乳素和IGFBP-1蛋白水平。 SF-EV的大小范围为50至300?nm,它们表达外泌体标记(ALIX,SYNTENIN-1,CD9和CD81)。 SF-EV在相似的水平上绑定到非蜕皮化和蜕皮化的ESC。一次(p = 0.0044)和多次(p = 0.0021)SF-EV暴露后,ESC催乳素分泌增加。在IGFBP-1蛋白水平上没有发现差异。总之,SF-EVs可增强体外ESC蜕膜作用并增加催乳素的分泌,催乳素是植入过程中的必需激素。这阐明了SF-EV对子宫内膜容受性的新作用。缩写:ECACC:欧洲认证的细胞培养物; ESC:子宫内膜间质细胞;电动汽车:细胞外囊泡; FCS:胎牛血清; HRP:辣根过氧化物酶; IFNγ:γ干扰素; IGF:胰岛素样生长因子; IGFBP-1:胰岛素样生长因子结合蛋白1;试管婴儿:体外受精; MVB:多囊体; NTA:纳米颗粒跟踪分析; PRLR〜(?/?):纯合催乳素受体敲除; RT:室温; SF-EVs:精液细胞外囊泡; STR:短串联重复; TGFβ:转化生长因子β; uNK:子宫自然杀手

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