| First Author | Zheng B | Year | 2024 |
| Journal | iScience | Volume | 27 |
| Issue | 7 | Pages | 110293 |
| PubMed ID | 39050703 | Mgi Jnum | J:352147 |
| Mgi Id | MGI:7704760 | Doi | 10.1016/j.isci.2024.110293 |
| Citation | Zheng B, et al. (2024) Type III adenylyl cyclase is essential for follicular development in female mice and their reproductive lifespan. iScience 27(7):110293 |
| abstractText | Premature ovarian failure (POF) is a complex and heterogeneous disease that causes infertility and subfertility. However, the molecular mechanism of POF has not been fully elucidated. Here, we show that the loss of adenylyl cyclase III (Adcy3) in female mice leads to POF and a shortened reproductive lifespan. We found that Adcy3 is abundantly expressed in mouse oocytes. Adcy3 knockout mice exhibited the excessive activation of primordial follicles, progressive follicle loss, follicular atresia, and ultimately POF. Mechanistically, we found that mitochondrial oxidative stress in oocytes significantly increased with age in Adcy3-deficient mice and was accompanied by oocyte apoptosis and defective folliculogenesis. In contrast, compared with wild-type female mice, humanized ADCY3 knock-in female mice exhibited improved fertility with age. Collectively, these results reveal that the previously unrecognized Adcy3 signaling pathway is tightly linked to female ovarian aging, providing potential pharmaceutical targets for preventing and treating POF. |
