Neonatal Mouse Ovary Culture: An In Vitro Model for Studying Primordial Follicle Regulation

Abstract

In mammalian females, primordial follicles form during fetal ovarian development and serve as the only source to sustain adult ovarian function. Mechanisms underlying how primordial follicles assemble, maintain dormancy, activate for follicular development, and undergo cell death are important for understanding ovarian physiology and pathological conditions. Here, we demonstrate a protocol of culturing postnatal mouse ovaries on membrane inserts - an approach allowing culture, pharmaceutical treatment, and live-imaging of intact ovaries for up to 10 days depending on the developmental stage of the ovary. The change of culture conditions can be done by transferring inserts containing cultured ovaries between wells on a plate, avoiding physical interference with tissues during culture. In this experiment, we use postnatal day 5 (P5) CD1 mouse ovary culture as an example. P5 ovaries were isolated and placed on a 12 mm insert in a 24-well plate. Each ovary was separated within a droplet of DMEM/F12 medium supplemented with 10% FBS, 3 mg/ml BSA, 10 mIU/ml FSH, and Gibco Antibiotic-Antimycotic, and gently stabilized to the membrane insert. The medium was changed every two days, and the culture was maintained for five days. Following the culture, ovaries were fixed in 4% paraformaldehyde for two hours and processed for whole-mount antibody staining. Primordial follicles were visualized using confocal microscopy with anti-DDX4 antibody, allowing for the analysis of oocyte number and morphology. We showed that the number of primordial follicles in each ovary was significantly affected by whether tissues were properly placed on the membrane insert. Difference in the number of ovaries on each insert may contribute to non-biological variations and should be avoided.