RRC ID 89867
Author Zhang Y, Hu Y, Xu Y, Kuai Y, Wang S, Yu J.
Title Androgen promotes oocyte development by upregulating gap junction intercellular communication activity in granulosa cells in mice.
Journal PeerJ
Abstract BACKGROUND:Recent studies have highlighted the role of androgen in poor ovarian response (POR). However, the mechanisms by which androgen works, particularly in older POR patients, remain unclear. The study aimed to investigate the effects of androgen on granulosa cells and to explore the underlying mechanisms preliminarily.
METHODS:Elderly female C57BL/6J mice were treated with various concentrations of dehydroepiandrosterone (DHEA) in vivo. Granulosa cells were exposed to different concentrations of testosterone (T), flutamide (an androgen receptor antagonist, AR antagonist), and GF109203X (a protein kinase C inhibitor, PKC inhibitor) in vitro. Gap junction intercellular communication (GJIC) activity was analyzed using the scrape loading/dye transfer technique.
RESULTS:DHEA treatment significantly increased serum DHEA, T, and anti-Müllerian hormone levels, as well as the number of oocytes harvested. Treatment with T within the physiological concentration range significantly increased GJIC activity. These effects of T were partially counteracted by flutamide or GF109203X.
CONCLUSIONS:Androgen may enhance GJIC activity in granulosa cells via the AR pathway and PKC signaling pathway, an effect associated with improved oocyte development in mice. The findings provide a theoretical basis for the use of androgen pretreatment to improve ovarian response in older POR patients.
Volume 14
Pages e21194
Published 2026-1-1
DOI 10.7717/peerj.21194
PII 21194
PMID 42083638
PMC PMC13135750
MeSH Androgens* / pharmacology Animals Cell Communication* / drug effects Dehydroepiandrosterone / pharmacology Female Flutamide / pharmacology Gap Junctions* / drug effects Gap Junctions* / metabolism Granulosa Cells* / drug effects Granulosa Cells* / metabolism Indoles / pharmacology Maleimides / pharmacology Mice Mice, Inbred C57BL Oocytes* / drug effects Oocytes* / growth & development Protein Kinase C / metabolism Testosterone / blood Testosterone / pharmacology Up-Regulation
Resource
Human and Animal Cells KGN(RCB1154)