Komatsu Kouji, Iwase Akira, Murase Tomohiko, Masubuchi Satoru
Department of Physiology, Aichi Medical University;
Department of Obstetrics and Gynecology, Nagoya University Graduate School of Medicine; Department of Maternal and Perinatal Medicine, Nagoya University Hospital.
J Vis Exp. 2018 Jun 19(136):57794. doi: 10.3791/57794.
Mammalian females periodically ovulate an almost constant number of oocytes during each estrus cycle. To sustain such regularity and periodicity, regulation occurs at the hypothalamic-pituitary-gonadal axis level and on developing follicles in the ovary. Despite active studies, follicle development mechanisms are not clear because of the several steps involved from the dormant primordial follicle activation to ovulation, and because of the regulation complexity that differs at each follicular stage. To investigate the mechanisms of follicle development, and the dynamics of follicles throughout the estrus cycle, we developed a mouse ovarian tissue culture model that can be used to observe follicle development using a microscope. Systematic follicle development, periodical ovulation, and follicle atresia can all be reproduced in the cultured ovary model, and the culture conditions can be experimentally modulated. Here, we demonstrate the usefulness of this method in the study of the regulatory mechanisms of follicle development and other ovarian phenomena.
在每个发情周期中,哺乳动物雌性会定期排出数量几乎恒定的卵母细胞。为维持这种规律性和周期性,调节作用发生在下丘脑 - 垂体 - 性腺轴水平以及卵巢中发育的卵泡上。尽管进行了大量研究,但由于从静止的原始卵泡激活到排卵涉及多个步骤,且每个卵泡阶段的调节复杂性不同,卵泡发育机制仍不清楚。为了研究卵泡发育机制以及整个发情周期中卵泡的动态变化,我们建立了一种小鼠卵巢组织培养模型,该模型可用于通过显微镜观察卵泡发育。在培养的卵巢模型中可以重现系统性的卵泡发育、周期性排卵和卵泡闭锁,并且培养条件可以通过实验进行调节。在此,我们证明了该方法在研究卵泡发育调节机制和其他卵巢现象中的实用性。