Thompson Jeremy G, Brown Hannah M, Kind Karen L, Russell Darryl L
Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia School of Paediatrics and Reproductive Health, The University of Adelaide, Adelaide, South Australia, Australia Australian Research Council Centre of Excellence for Nanoscale BioPhotonics, The University of Adelaide, Adelaide, South Australia, Australia
Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia School of Paediatrics and Reproductive Health, The University of Adelaide, Adelaide, South Australia, Australia Australian Research Council Centre of Excellence for Nanoscale BioPhotonics, The University of Adelaide, Adelaide, South Australia, Australia.
Biol Reprod. 2015 Jun;92(6):153. doi: 10.1095/biolreprod.115.128660. Epub 2015 May 13.
Oocytes within antral follicles are thought to have restricted access to O2, as follicle vascularity is not adjacent and both granulosa and cumulus cells are metabolically active. Indeed, measured follicular antrum partial pressure (pO2) is regarded as low, but accurate and direct measurement represents a technical challenge that has yet to be overcome. The oocyte itself is highly dependent on oxidative phosphorylation for survival and competence for further development following fertilization, and it has been suggested that follicular pO2 levels are correlated with this capacity for further development. It is clear that gonadotropins are involved in regulating antrum formation, follicle vascularization, cellular differentiation, and the hypoxia-inducible factors (HIF), which are mainly regulated by dissolved O2 concentration. A newly discovered player in this story is the intracellular production of hemoglobin by both granulosa and cumulus cells, as well as the oocyte. Furthermore, cellular hemoglobin levels are dynamic, responding to the ovulatory luteinizing hormone (LH) surge. We hypothesize that this gas transport and antioxidant molecule is involved in the prevention of hypoxic response signaling by HIFs within the preovulatory antral follicle; and the transition of granulosa cells to luteal tissue by facilitating the stabilization of HIFs, enabling induction of luteinization signaling. Another possible role is by sequestering nitric oxide (NO) during the ovulatory period, which may facilitate the resumption of meiosis in the oocyte. Testing these hypotheses will be challenging but important if the regulation of ovarian function is to be fully understood.
有腔卵泡内的卵母细胞被认为获取氧气的途径有限,因为卵泡血管并不相邻,而且颗粒细胞和卵丘细胞都具有代谢活性。实际上,测得的卵泡腔分压(pO2)被认为较低,但准确且直接的测量是一项尚未克服的技术挑战。卵母细胞自身高度依赖氧化磷酸化来维持生存以及受精后进一步发育的能力,并且有人提出卵泡pO2水平与这种进一步发育的能力相关。很明显,促性腺激素参与调节卵泡腔形成、卵泡血管生成、细胞分化以及缺氧诱导因子(HIF),而这些主要受溶解氧浓度调节。在这个过程中一个新发现的因素是颗粒细胞、卵丘细胞以及卵母细胞内血红蛋白的产生。此外,细胞内血红蛋白水平是动态的,对排卵时促黄体生成素(LH)高峰有反应。我们假设这种气体运输和抗氧化分子参与了排卵前有腔卵泡内HIFs缺氧反应信号的预防;并且通过促进HIFs的稳定,使颗粒细胞向黄体组织转变,从而诱导黄体化信号。另一个可能的作用是在排卵期间螯合一氧化氮(NO),这可能有助于卵母细胞减数分裂的恢复。如果要全面了解卵巢功能的调节,验证这些假设将具有挑战性但很重要。