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Autor(en) / Beteiligte
Titel
Brown adipose tissue‐derived exosomes improve polycystic ovary syndrome in mice via STAT3/GPX4 signaling pathway
Ist Teil von
  • The FASEB journal, 2024-09, Vol.38 (18), p.e70062-n/a
Ort / Verlag
United States
Erscheinungsjahr
2024
Quelle
MEDLINE
Beschreibungen/Notizen
  • Polycystic ovary syndrome (PCOS) is associated with impaired adipose tissue physiology. Elevated brown adipose tissue (BAT) mass or activity has shown potential in the treatment of PCOS. In this study, we aimed to investigate whether BAT‐derived exosomes (BAT‐Exos), as potential biomarkers of BAT activity, exert similar benefits as BAT in the treatment of PCOS. PCOS was induced in female C57BL/6J mice orally administered 1 mg/kg of letrozole for 21 days. Subsequently, the animals underwent transplantation with BAT or administered BAT‐Exos (200 μg) isolated from young healthy mice via the tail vein; healthy female mice were used as controls. The results indicate that BAT‐Exos treatment significantly reduced body weight and improved insulin resistance in PCOS mice. In addition, BAT‐Exos improved ovulation function by reversing the acyclicity of the estrous cycle, decreasing circulating luteinizing hormone and testosterone, recovering ovarian performance, and improving oocyte quality, leading to a higher pregnancy rate and litter size. Furthermore, western blotting revealed reduced expression of signal transducer and activator of transcription 3 (STAT3) and increased expression of glutathione peroxidase 4 (GPX4) in the ovaries of mice in the BAT‐Exos group. To further explore the role of the STAT3/GPX4 signaling pathway in PCOS mice, we treated the mice with an intraperitoneal injection of 5 mg/kg stattic, a STAT3 inhibitor. Consistent with BAT‐Exos treatment, the administration of stattic rescued letrozole‐induced PCOS phenotypes. These findings suggest that BAT‐Exos treatment might be a potential therapeutic strategy for PCOS and that the STAT3/GPX4 signaling pathway is a critical therapeutic target for PCOS. Brown adipose tissue‐derived exosomes (BAT‐Exos) treatment significantly reduced body weight and improved insulin resistance and ovulation function, leading to a higher pregnancy rate and litter size in PCOS mice. In addition, the STAT3/GPX4 signaling pathway is a critical target of BAT‐Exos on the ovary in PCOS mice.

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