Investigation of FF-MAS oxysterole’s role in follicular development and its relation to hedgehog signal pathway

ArticleAçık Erişim

Özet

The Hedgehog signaling pathway plays a crucial role in folliculogenesis; however, the association between FF-MAS oxysterol activity in folliculogenesis and the Hedgehog signaling pathway has not been revealed. The evaluation of FF-MAS activity in polycystic ovary syndrome (PCOS) with folliculogenesis disorder might provide a new approach to tackle follicular and oocyte maturation failure. The question is: does FF-MAS oxysterol affect granulosa cell (GC) proliferation? If so, is this effect facilitated through the Hedgehog pathway? To answer these questions, GCs were isolated from follicle fluids obtained from patients undergoing oocyte retrieval during in vitro fertilization (IVF) treatment. After the isolated GCs were incubated in different cell culture media, the levels of Hedgehog pathway components (SMO, Gli1) were measured by using immunohistochemical methods, cytoELISA, and qRT-PCR. Meanwhile, cell proliferation rates were determined. Significant increases (p < 0.001) in SMO and Gli1 expressions and cell proliferation were observed in the FF-MAS-treated subgroups of both PCOS and male factor participants compared to the FF-MAS deficient subgroup. Remarkably, FF-MAS positively affected the pathway components despite the pathway inhibitor cyclopamine. Although the increase in Hedgehog pathway components was slightly higher in the male factor group (MF), it was not statistically significant. In our study, we demonstrated for the first time the molecular effect of FF-MAS on human GCs in folliculogenesis. Since FF-MAS is already used in assisted reproductive techniques in animals and is known to be synthesized in the human body, it could be considered a new approach in human IVF treatments. © The Author(s) 2024.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/11263Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1038/s41598-024-76281-5Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorZırh, Selim
dc.contributor.authorBahador Zırh, Elham
dc.contributor.authorErol, Süleyman
dc.contributor.authorKarakoç Sökmensüer, Lale
dc.contributor.authorBozdağ, Gürkan
dc.contributor.authorMüftüoğlu, Sevda Fatma
dc.date.accessioned2026-10-18T20:26:20.080330781Z
dc.date.available2026-10-18T20:26:20.080330781Z
dc.date.issued2024
dc.description.abstractThe Hedgehog signaling pathway plays a crucial role in folliculogenesis; however, the association between FF-MAS oxysterol activity in folliculogenesis and the Hedgehog signaling pathway has not been revealed. The evaluation of FF-MAS activity in polycystic ovary syndrome (PCOS) with folliculogenesis disorder might provide a new approach to tackle follicular and oocyte maturation failure. The question is: does FF-MAS oxysterol affect granulosa cell (GC) proliferation? If so, is this effect facilitated through the Hedgehog pathway? To answer these questions, GCs were isolated from follicle fluids obtained from patients undergoing oocyte retrieval during in vitro fertilization (IVF) treatment. After the isolated GCs were incubated in different cell culture media, the levels of Hedgehog pathway components (SMO, Gli1) were measured by using immunohistochemical methods, cytoELISA, and qRT-PCR. Meanwhile, cell proliferation rates were determined. Significant increases (p < 0.001) in SMO and Gli1 expressions and cell proliferation were observed in the FF-MAS-treated subgroups of both PCOS and male factor participants compared to the FF-MAS deficient subgroup. Remarkably, FF-MAS positively affected the pathway components despite the pathway inhibitor cyclopamine. Although the increase in Hedgehog pathway components was slightly higher in the male factor group (MF), it was not statistically significant. In our study, we demonstrated for the first time the molecular effect of FF-MAS on human GCs in folliculogenesis. Since FF-MAS is already used in assisted reproductive techniques in animals and is known to be synthesized in the human body, it could be considered a new approach in human IVF treatments. © The Author(s) 2024.
dc.description.sponsorshipFunding text 1: The subject\u2019s privacy and confidentiality were assured, and the study received approval from the Hacettepe University Research Ethics Committee (#GO 18/573-04) on June 12, 2018. This research benefited from a grant provided by the Hacettepe University Research Foundation (Grant No: TSA-2018-17320) and was carried out in compliance with the Helsinki Declaration, as revised in 2013. ; Funding text 2: Hacettepe University Research Foundation (Grant No: TSA-2018-17320).
dc.identifier.doi10.1038/s41598-024-76281-5
dc.identifier.issn2045-2322
dc.identifier.issue1
dc.identifier.pmcidPMC11496726
dc.identifier.pmid39438722
dc.identifier.scopus2-s2.0-85207194455
dc.identifier.startpage24863
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/11263
dc.identifier.volume14
dc.identifier.wosWOS:001340425900127
dc.language.isoen
dc.publisherNature Research
dc.relation.ispartofScientific Reports
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectFF-MAS
dc.subjectFollicle development
dc.subjectGranulosa cells
dc.subjectOxysterols
dc.subjectPCOS
dc.subjectSteroidogenesis
dc.subjectAdult
dc.subjectCell Proliferation
dc.subjectFemale
dc.subjectFertilization in Vitro
dc.subjectFollicular Fluid
dc.subjectHedgehog Proteins
dc.subjectHumans
dc.subjectOvarian Follicle
dc.subjectPolycystic Ovary Syndrome
dc.subjectSignal Transduction
dc.subjectSmoothened Receptor
dc.subjectZinc Finger Protein GLI1
dc.subjectGLI1 protein, human
dc.subjectoxysterol
dc.subjectSMO protein, human
dc.subjectSmoothened protein
dc.subjectsonic hedgehog protein
dc.subjecttranscription factor Gli1
dc.subjectgenetics
dc.subjectgranulosa cell
dc.subjecthuman
dc.subjectin vitro fertilization
dc.subjectmetabolism
dc.subjectovary follicle
dc.titleInvestigation of FF-MAS oxysterole’s role in follicular development and its relation to hedgehog signal pathway
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus0
rdl.citation.wos0
rdl.departmentFaculty of Medicine, Department of Histology and Embryology, Erzincan Binali Yıldırım University, Erzincan, Turkey.
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)