V. I. Kulakov National Medical Research Center for Obstetrics, Gynecology, and Perinatology, Ministry of Health of the Russian Federation, Moscow, Russia.
A. N. Belozersky Research Institute of Physical and Chemical Biology, M. V. Lomonosov Moscow State University, Moscow, Russia.
Bull Exp Biol Med. 2021 Dec;172(2):254-262. doi: 10.1007/s10517-021-05372-4. Epub 2021 Dec 2.
We studied the effect of extracellular vesicles of the follicular fluid on morphofunctional characteristics of human spermatozoa using CASA (computer-assisted sperm analysis) analytical system. The vesicles were obtained by sequential centrifugation at different rotational speeds and frozen at -80°C in the Sydney IVF Gamete Buffer medium. The sperm fraction was isolated from the seminal fluid of 21 patients aged 27-36 years by differential centrifugation in a density gradient. The precipitate was suspended in Sydney IVF Gamete Buffer to a concentration of 10/ml and incubated with vesicles (1:2) at 37°C in a CO incubator for 30 min and 1 h. Sperm fraction incubated without vesicles served as the control. After incubation, some sperm samples were centrifuged at 700g for 5 min and fixed in 2.5% glutaraldehyde in 0.1 M buffer for transmission electron microscopy. After 30-min and 1-h incubation, the progressive and total sperm motility improved, the curvilinear and linear velocity of spermatozoa did not change significantly. Incubation with vesicles significantly changed the trajectory of sperm movement, which can attest to an increase in their hyperactivation and, probably, fertilizing capacity. Analysis of the effect of extracellular vesicles of follicular fluid on sperm motility will help to improve the effectiveness of assisted reproductive technology programs with male infertility factor by improving sperm characteristics in patients with asthenozoospermia and increasing the fertilizing ability of the sperm.
我们使用 CASA(计算机辅助精子分析)分析系统研究了卵泡液外囊泡对人精子形态功能特征的影响。囊泡通过在不同转速下进行连续离心获得,并在 -80°C 的 Sydney IVF 配子缓冲液中冷冻。精子部分通过在密度梯度中的差速离心从 21 名年龄在 27-36 岁的患者的精液中分离出来。沉淀悬浮在 Sydney IVF 配子缓冲液中,浓度为 10/ml,并在 CO 孵育箱中与囊泡(1:2)在 37°C 下孵育 30 分钟和 1 小时。未孵育囊泡的精子部分作为对照。孵育后,一些精子样本在 700g 下离心 5 分钟,并在 0.1 M 缓冲液中的 2.5%戊二醛中固定,用于透射电子显微镜检查。孵育 30 分钟和 1 小时后,精子的渐进性和总运动能力得到改善,精子的曲线和直线速度没有明显变化。囊泡孵育显著改变了精子运动的轨迹,这可以证明它们的超激活能力增加,可能提高了受精能力。分析卵泡液外囊泡对精子运动的影响有助于通过改善少精症患者的精子特征和提高精子的受精能力来提高男性不育因素的辅助生殖技术方案的有效性。