Improvement of human sperm vacuolization and DNA fragmentation co-cultured with adipose-derived mesenchymal stem cell secretome: In vitro effect

dc.contributor.authorBader, Robert
dc.contributor.authorIbrahim, José Noel
dc.contributor.authorMourad, Ali
dc.contributor.authorMoussa, Mayssam
dc.contributor.authorAzoury, Joan
dc.contributor.authorAzoury, Joseph
dc.contributor.authorAlaaeddine, Nada M.
dc.contributor.departmentObstetrics and Gynecology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T12:08:02Z
dc.date.available2025-01-24T12:08:02Z
dc.date.issued2019
dc.description.abstractBackground and Objectives: Oxidative stress (OS) is known to be an important factor of male infertility. Adipose-derived mesenchymal stem cells (AD-MSCs) are known to have immune-modulatory and anti-oxidant effects through their secretions, hence raising the idea of their potential benefit to improve sperm parameters. This study aims at investigating the effect of AD-MSCs conditioned medium (CM) on human sperm parameters in the presence and absence of H2O2-induced OS. Methods and Results: Sperm samples were collected from 30 healthy men and divided into two groups: non-stressed and H2O2-stressed. Isolated AD-MSCs from healthy donors undergoing liposuction were cultured and CM was collected at 24, 48 and 72 h. Both sperm groups were cultured with CM and a time course was performed followed by an evaluation of sperm parameters. The incubation of non-stressed and stressed sperm samples with AD-MSCs-CM for 24 h was found to have the optimum impact on sperm vacuolization, DNA fragmentation and OS levels in comparison to other incubation timings, while preserving motility, viability and morphology of cells. Incubation with CM improved all sperm parameters except morphology in comparison to the non-treated group, with the best effect noted with CM collected at 24 h rather than 48 or 72 h for sperm vacuolization and DNA fragmentation. When compared to fresh semen parameters (T0), samples cultured with CM 24 h showed a significant decrease in sperm vacuolization and DNA fragmentation while keeping other parameters stable. Conclusions: AD-MSCSs-CM improves sperm quality, and hence can be used in treating infertility and subsequently enhancing IVF outcomes. © 2019 by the Korean Society for Stem Cell Research.
dc.identifier.doihttps://doi.org/10.15283/ijsc19047
dc.identifier.eid2-s2.0-85076176169
dc.identifier.urihttp://hdl.handle.net/10938/31690
dc.language.isoen
dc.publisherSungkyunkwan University
dc.relation.ispartofInternational Journal of Stem Cells
dc.sourceScopus
dc.subjectConditioned medium
dc.subjectMale infertility
dc.subjectMesenchymal stem cells
dc.subjectOxidative stress
dc.subjectSperm
dc.subjectHydrogen peroxide
dc.subjectAdipose derived stem cell
dc.subjectAdult
dc.subjectArticle
dc.subjectCalcification
dc.subjectCell differentiation
dc.subjectCell structure
dc.subjectCell vacuole
dc.subjectCell viability
dc.subjectCellular secretion
dc.subjectComparative study
dc.subjectDna fragmentation
dc.subjectHuman
dc.subjectHuman cell
dc.subjectHuman tissue
dc.subjectImmunophenotyping
dc.subjectIn vitro study
dc.subjectLiposuction
dc.subjectMale
dc.subjectMesenchymal stem cell
dc.subjectNormal human
dc.subjectSperm quality
dc.subjectSpermatozoon motility
dc.titleImprovement of human sperm vacuolization and DNA fragmentation co-cultured with adipose-derived mesenchymal stem cell secretome: In vitro effect
dc.typeArticle

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