Uptake Assay of Ram Seminal Plasma Extracellular Vesicles to Sperm.

IF 1.1 Q3 BIOLOGY
Tomas Armani, Anabella R Nicolli, Lucia Zalazar, Juan I Lobo, Monserrat Buendía Arellano, Federico A Hozbor, Sofia Rio, Silvina Perez Martinez, Andreina Cesari
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引用次数: 0

Abstract

Extracellular vesicles (EVs) are critical mediators of cell-cell communication and play a key role in male reproductive biology by modulating sperm function. This protocol describes a robust and reproducible workflow for isolating EVs from ram seminal plasma using size-exclusion chromatography (SEC) and assessing their uptake by ram spermatozoa. In contrast to ultracentrifugation-based methods, SEC provides a gentle and more efficient isolation approach that preserves EV integrity and functionality. A central innovation of this protocol is the use of carboxyfluorescein succinimidyl ester (CFSE)-labeled seminal plasma EVs (SP-EVs) to evaluate their incorporation into sperm cells through two complementary detection platforms: (i) flow cytometry with standard resolution and (ii) confocal microscopy, for spatial confirmation of EV-sperm interactions. By bridging the gap between EV isolation and functional analysis, this protocol provides a valuable tool for investigating the role of EV-cell interactions. Specifically, it offers potential applications in male fertility preservation, biomarker discovery, and the development of EV-based therapeutic strategies in reproductive medicine. Key features • Provides a gentle, SEC-based EV isolation method optimized for ram seminal plasma, suitable for preserving vesicle integrity in studies of male reproductive biology. • Integrates EV purification with functional assays, enabling direct evaluation of EV-sperm interactions through confocal microscopy and flow cytometry. • Includes a reproducible CFSE-labeling strategy tailored for seminal plasma EVs, ensuring consistent detection of vesicle uptake by ram spermatozoa. • Designed for applications in fertility research, offering a workflow compatible with biomarker discovery, cryopreservation studies, and development of EV-based reproductive interventions.

公羊精浆细胞外囊泡对精子的吸收测定。
细胞外囊泡(EVs)是细胞间通讯的重要介质,通过调节精子功能在男性生殖生物学中起着关键作用。该方案描述了一种稳健且可重复的工作流程,用于使用尺寸排除色谱(SEC)从公羊精浆中分离ev并评估其被公羊精子摄取。与基于超离心的方法相比,SEC提供了一种温和且更有效的分离方法,可以保持EV的完整性和功能。该方案的核心创新是使用羧基荧光素琥珀酰酰酯(CFSE)标记的精浆ev (sp - ev)通过两个互补的检测平台来评估它们与精子细胞的结合情况:(i)标准分辨率的流式细胞术和(ii)共聚焦显微镜,用于空间确认ev -精子相互作用。通过弥合EV分离和功能分析之间的差距,该协议为研究EV-细胞相互作用的作用提供了有价值的工具。具体来说,它在男性生育能力保存、生物标志物发现和基于ev的生殖医学治疗策略的发展方面具有潜在的应用前景。•提供了一种温和的,基于sec的EV分离方法,优化了公羊精浆,适用于在男性生殖生物学研究中保存囊泡完整性。•整合EV纯化与功能分析,使EV-精子相互作用通过共聚焦显微镜和流式细胞术直接评估。•包括为精浆ev量身定制的可重复cfse标记策略,确保公羊精子对囊泡摄取的一致检测。•专为生育研究应用而设计,提供与生物标志物发现,低温保存研究和基于ev的生殖干预开发兼容的工作流程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
1.50
自引率
0.00%
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