Tomas Armani, Anabella R Nicolli, Lucia Zalazar, Juan I Lobo, Monserrat Buendía Arellano, Federico A Hozbor, Sofia Rio, Silvina Perez Martinez, Andreina Cesari
{"title":"Uptake Assay of Ram Seminal Plasma Extracellular Vesicles to Sperm.","authors":"Tomas Armani, Anabella R Nicolli, Lucia Zalazar, Juan I Lobo, Monserrat Buendía Arellano, Federico A Hozbor, Sofia Rio, Silvina Perez Martinez, Andreina Cesari","doi":"10.21769/BioProtoc.5653","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":93907,"journal":{"name":"Bio-protocol","volume":"16 7","pages":"e5653"},"PeriodicalIF":1.1000,"publicationDate":"2026-04-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13067157/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bio-protocol","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21769/BioProtoc.5653","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOLOGY","Score":null,"Total":0}
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.