Mellisho Edwin A, Velásquez Alejandra E, Nuñez María J, Cabezas Joel G, Cueto Juan A, Fader Claudio, Castro Fidel O, Rodríguez-Álvarez Lleretny
Laboratory of Animal Biotechnology, Department of Animal Science, Faculty of Veterinary Science, University of Concepción, Chillán, Concepción, Chile.
Laboratory of Cell and Molecular Biology, IHEM-CONICET, Faculty of Medical Sciences, National University of Cuyo, Mendoza, Argentina.
PLoS One. 2017 May 25;12(5):e0178306. doi: 10.1371/journal.pone.0178306. eCollection 2017.
Extracellular vesicles (EVs) have been identified within different body fluids and cell culture media. However, there is very little information on the secretion of these vesicles during early embryonic development. The aims of this work were first to demonstrate the secretion of extracellular vesicles by pre-implantation bovine embryos and second to identify and characterize the population of EVs secreted by bovine blastocysts during the period from day seven to nine of embryo culture and its correlation with further embryo development up to day 11. Bovine embryos were produced by in vitro fertilization (IVF) or parthenogenetic activation (PA) and cultured until blastocyst stage. Blastocyst selection was performed at day 7 post IVF/PA considering two variables: stage of development and quality of embryos. Selected blastocysts were cultured in vitro for 48 hours in groups (exp. 1) or individually (exp. 2) in SOF media depleted of exosomes. At day 9 post IVF/PA the media was collected and EVs isolated by ultracentrifugation. Transmission electron microscopy revealed the presence of heterogeneous vesicles of different sizes and population: microvesicles (MVs) and exosomes (EXs) of rounded shape, enclosed by a lipid bi-layer and ranging from 30 to 385 nm of diameter. Flow cytometry analysis allowed identifying CD63 and CD9 proteins as exosome markers. Nanoparticle tracking analysis generated a large number of variables, which required the use of multivariate statistics. The results indicated that the concentration of vesicles is higher in those blastocysts with arrested development from day 9 up to day 11 of in vitro development (6.7 x 108 particles/ml) derived from IVF (p <0.05), compared to PA blastocysts (4.7 x 108 particles/ml). Likewise, the profile (concentration and diameter) of particles secreted by embryos derived from IVF were different from those secreted by PA embryos. In conclusion, we demonstrated that bovine blastocysts secrete MVs/EXs to the culture media. Data suggest that characteristics of the population of EVs vary depending on embryo competence.
细胞外囊泡(EVs)已在不同体液和细胞培养基中被鉴定出来。然而,关于这些囊泡在早期胚胎发育过程中的分泌情况,相关信息非常少。本研究的目的,一是证明植入前牛胚胎可分泌细胞外囊泡,二是鉴定和表征牛囊胚在胚胎培养第7天至第9天期间分泌的细胞外囊泡群体,并确定其与胚胎发育至第11天的进一步发育情况之间的相关性。通过体外受精(IVF)或孤雌激活(PA)产生牛胚胎,并培养至囊胚阶段。在IVF/PA后第7天进行囊胚选择,考虑两个变量:发育阶段和胚胎质量。将选定的囊胚分组(实验1)或单独(实验2)在不含外泌体的SOF培养基中体外培养48小时。在IVF/PA后第9天收集培养基,并通过超速离心分离细胞外囊泡。透射电子显微镜显示存在不同大小和群体的异质囊泡:圆形的微囊泡(MVs)和外泌体(EXs),被脂质双层包围,直径范围为30至385纳米。流式细胞术分析可将CD63和CD9蛋白鉴定为外泌体标志物。纳米颗粒跟踪分析产生了大量变量,这需要使用多变量统计方法。结果表明,与孤雌激活囊胚(4.7×10⁸个颗粒/毫升)相比,在体外发育第9天至第11天发育停滞的体外受精来源囊胚(6.7×10⁸个颗粒/毫升)中的囊泡浓度更高(p<0.05)。同样,体外受精来源胚胎分泌的颗粒特征(浓度和直径)与孤雌激活胚胎分泌的颗粒不同。总之,我们证明了牛囊胚可向培养基中分泌微囊泡/外泌体。数据表明,细胞外囊泡群体的特征因胚胎能力而异。