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Status: Bibliographieeintrag

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Verfasst von:Nguyen, Xuan Phuoc [VerfasserIn]   i
 Vilkaite, Adriana [VerfasserIn]   i
 Bender, Ulrike [VerfasserIn]   i
 Dietrich, Jens Erik [VerfasserIn]   i
 Hinderhofer, Katrin [VerfasserIn]   i
 Strowitzki, Thomas [VerfasserIn]   i
 Rehnitz, Julia [VerfasserIn]   i
Titel:Regulation of bone morphogenetic protein receptor type II expression by FMR1/Fragile X mental retardation protein in human granulosa cells in the context of poor ovarian response
Verf.angabe:Xuan Phuoc Nguyen, Adriana Vilkaite, Ulrike Bender, Jens E. Dietrich, Katrin Hinderhofer, Thomas Strowitzki and Julia Rehnitz
E-Jahr:2024
Jahr:3 October 2024
Umfang:14 S.
Illustrationen:Illustrationen
Fussnoten:Gesehen am 26.03.2025
Weitere Titel:Titel des special issue: Research on Transcriptional Regulation in Reproductive Biology
Titel Quelle:Enthalten in: International journal of molecular sciences
Ort Quelle:Basel : Molecular Diversity Preservation International, 2000
Jahr Quelle:2024
Band/Heft Quelle:25(2024), 19, special issue, Artikel-ID 10643, Seite 1-14
ISSN Quelle:1422-0067
 1661-6596
Abstract:Fragile X mental retardation protein (FMRP) is a translational repressor encoded by FMR1. It targets bone morphogenetic protein receptor type II (BMPR2), which regulates granulosa cell (GC) function and follicle development. However, whether this interaction affects folliculogenesis remains unclear. Therefore, this study investigated the potential effect of FMRP-BMPR2 dysregulation in ovarian reserves and infertility. COV434 cells and patient-derived GCs were used to evaluate FMRP and BMPR2 expression. Similarly, FMR1, BMPR2, LIMK1, and SMAD expression were evaluated in GCs with normal (NOR) and poor (POR) ovarian responses. FMRP and BMPR2 were expressed in both cell types. They were co-localized to the nuclear membrane of COV434 cells and cytoplasm of primary GCs. FMR1 silencing increased the mRNA and protein levels of BMPR2. However, the mRNA levels of FMR1 and BMPR2 were significantly lower in the POR group. FMR1 and BMPR2 levels were strongly positively correlated in the NOR group but weakly correlated in the POR group. Additionally, SMAD9 expression was significantly reduced in the POR group. This study highlights the crucial role of FMR1/FMRP in the regulation of BMPR2 expression and its impact on ovarian function. These findings indicate that the disruption of FMRP-BMPR2 interactions may cause poor ovarian responses and infertility.
DOI:doi:10.3390/ijms251910643
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

kostenfrei: Volltext: https://doi.org/10.3390/ijms251910643
 kostenfrei: Volltext: https://www.mdpi.com/1422-0067/25/19/10643
 DOI: https://doi.org/10.3390/ijms251910643
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:BMPR2
 FMRP
 folliculogenesis
 granulosa cells
 infertility
 poor ovarian response
K10plus-PPN:1920619771
Verknüpfungen:→ Zeitschrift

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