| First Author | Jiang R | Year | 2022 |
| Journal | Cell Death Dis | Volume | 13 |
| Issue | 9 | Pages | 757 |
| PubMed ID | 36056002 | Mgi Jnum | J:328236 |
| Mgi Id | MGI:7335298 | Doi | 10.1038/s41419-022-05184-y |
| Citation | Jiang R, et al. (2022) CDC42 governs normal oviduct multiciliogenesis through activating AKT to ensure timely embryo transport. Cell Death Dis 13(9):757 |
| abstractText | Ciliated and secretory cells are two major cell types that comprise the oviduct epithelia. Accumulating evidences support a role of oviductal multiciliated epithelia for embryo transport, however the mechanisms underlying this specialized cell type differentiation remain elusive. Here, we report that CDC42 depletion in oviduct epithelia hampers the morphogenesis of multiciliated cell, and results in embryo retention, leading to early pregnancy failure. Utilizing the oviduct organoid model, we further observed that CDC42 guides secretory cells transition into multiciliated cells independent of its GTPase activity and the well-known Notch pathway. Further exploration uncovered the AKT as a novel indispensable regulator for multiciliated cells differentiation, whose activity was maintained by CDC42 through interacting with the p110beta. Consistently, re-activating AKT partially incites multiciliated cells differentiation in Cdc42 knockout oviductal organoids. Finally, low levels of CDC42 and phospho-AKT with reduced multiciliated cells in the oviduct are observed in women with ectopic pregnancy. Collectively, we provide previously unappreciated evidence that CDC42-AKT signaling is a critical determinant for morphogenesis of oviduct multiciliated cell, which possesses the clinical application in understanding the pathology of ectopic pregnancy and facilitating the development of prevention strategies. |
