INRA, UMR85 Physiologie de la Reproduction et des Comportements, F-37380 Nouzilly, France; Fertility and Research Centre, School of Women's and Children's Health, University of New South Wales, Sydney, NSW, Australia.
Fertility and Research Centre, School of Women's and Children's Health, University of New South Wales, Sydney, NSW, Australia.
Reprod Biomed Online. 2018 May;36(5):491-499. doi: 10.1016/j.rbmo.2018.01.014. Epub 2018 Feb 13.
Ovarian tissue is increasingly being collected from cancer patients and cryopreserved for fertility preservation. While the only available option to restore fertility is autologous transplantation, this treatment is not appropriate for all patients due to the risk of reintroducing cancer cells and causing disease recurrence. Harnessing the full reproductive potential of this tissue to restore fertility requires the development of culture systems that support oocyte development from the primordial follicle stage. While this has been achieved in the mouse, the goal of obtaining oocytes of sufficient quality to support embryo development has not been reached in higher mammals despite decades of effort. In vivo, primordial follicles gradually exit the resting pool, whereas when primordial follicles are placed into culture, global activation of these follicles occurs. Therefore, the addition of a factor(s) that can regulate primordial follicle activation in vitro may be beneficial to the development of culture systems for ovarian tissue from cancer patients. Several factors have been observed to inhibit follicle activation, including anti-Müllerian hormone, stromal-derived factor 1 and members of the c-Jun-N-terminal kinase pathway. This review summarizes the findings from studies of these factors and discusses their potential integration into ovarian tissue culture strategies for fertility preservation.
卵巢组织越来越多地从癌症患者中采集并冷冻保存,以用于生育力保存。虽然恢复生育力的唯一可行方法是自体移植,但由于存在重新引入癌细胞并导致疾病复发的风险,这种治疗方法并不适用于所有患者。为了充分发挥这种组织的生殖潜力,恢复生育力,需要开发支持从原始卵泡阶段发育卵母细胞的培养体系。虽然这在小鼠中已经实现,但尽管经过几十年的努力,仍未能在高等哺乳动物中获得足以支持胚胎发育的高质量卵母细胞。在体内,原始卵泡逐渐退出休眠池,而当原始卵泡被放入培养物中时,这些卵泡会发生全局激活。因此,添加一种(些)可以调节体外原始卵泡激活的因子可能有利于开发用于癌症患者卵巢组织的培养系统。已经观察到一些因素可以抑制卵泡激活,包括抗苗勒管激素、基质衍生因子 1 和 c-Jun-N 末端激酶途径的成员。本文综述了这些因素的研究结果,并讨论了它们在生育力保存的卵巢组织培养策略中的潜在应用。