Depletion of placental brain-derived neurotrophic factor (BDNF) is attributed to premature ovarian insufficiency (POI) in mice offspring

• Published in: Journal of ovarian research 2024-07, Vol.17 (1), p.141-17, Article 141
• Main Authors: Liu, Bin, Liu, Yongjie, Li, Shuman, Chen, Pingping, Zhang, Jun, Feng, Liping
• Format: Article
• Language: English
• Subjects: Analysis; Animals; BDNF; Brain-derived neurotrophic factor; Brain-Derived Neurotrophic Factor - genetics; Brain-Derived Neurotrophic Factor - metabolism; Cre; Disease Models, Animal; Female; Follicles; Gene expression; Health aspects; Immunohistochemistry; Menopause; Methods; Mice; Mice, Knockout; Oocyte; Oocytes - metabolism; Ovary - metabolism; Ovary - pathology; PGC; Physiological aspects; Placenta - metabolism; Pregnancy; Primary Ovarian Insufficiency - genetics; Primary Ovarian Insufficiency - metabolism; Primary Ovarian Insufficiency - pathology; RNAseq
• ISSN: 1757-2215; 1757-2215
• DOI: 10.1186/s13048-024-01467-4

Premature ovarian insufficiency (POI) is one of the causes of female infertility. Unexplained POI is increasingly affecting women in their reproductive years. However, the etiology of POI is diverse and remains elusive. We and others have shown that brain-derived neurotrophic factor (BDNF) plays an important role in adult ovarian function. Here, we report on a novel role of BDNF in the Developmental Origins of POI. Placental BDNF knockout mice were created using CRISPR/CAS9. Homozygous knockout (cKO(HO)) mice didn't survive, while heterozygous knockout (cKO(HE)) mice did. BDNF reduction in cKO(HE) mice was confirmed via immunohistochemistry and Western blots. Ovaries were collected from cKO(HE) mice at various ages, analyzing ovarian metrics, FSH expression, and litter sizes. In one-month-old mice, oocyte numbers were assessed using super-ovulation, and oocyte gene expression was analyzed with smart RNAseq. Ovaries of P7 mice were studied with SEM, and gene expression was confirmed with RT-qPCR. Alkaline phosphatase staining at E11.5 and immunofluorescence for cyclinD1 assessed germ cell number and cell proliferation. cKO(HE) mice had decreased ovarian function and litter size in adulthood. They were insensitive to ovulation induction drugs manifested by lower oocyte release after superovulation in one-month-old cKO(HE) mice. The transcriptome and SEM results indicate that mitochondria-mediated cell death or aging might occur in cKO(HE) ovaries. Decreased placental BDNF led to diminished primordial germ cell proliferation at E11.5 and ovarian reserve which may underlie POI in adulthood. The current results showed decreased placental BDNF diminished primordial germ cell proliferation in female fetuses during pregnancy and POI in adulthood. Our findings can provide insights into understanding the underlying mechanisms of POI.