{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Zhang X"],"funding":["Fundamental Research Funds for the Central Universities","Program for the Top Young Talents in College of Animal Science and Technology at Nanjing Agricultural University","National Natural Science Foundation of China","Natural Science Foundation of Jiangsu Province"],"pagination":["12454"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9604301"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["23(20)"],"pubmed_abstract":["Under stress conditions, luteinizing hormone (LH)-mediated ovulation is inhibited, resulting in insufficient oocyte production and excretion during follicular development. When the body is stressed, a large amount of corticosterone (CORT) is generated, which will lead to a disorder of the body's endocrine system and damage to the body. Our previous work showed that CORT can block follicular development in mice. Since LH acts through binding with the luteinizing hormone receptor (<i>Lhcgr</i>), the present study aimed to investigate whether and how corticosterone (CORT) influences <i>Lhcgr</i> expression in mouse ovarian granulosa cells (GCs). For this purpose, three-week-old ICR female mice were injected intraperitoneally with pregnant mare serum gonadotropin (PMSG). In addition, the treatment group was injected with CORT (1 mg/mouse) at intervals of 8 h and the control group was injected with the same volume of methyl sulfoxide (DMSO). GCs were collected at 24 h, 48 h, and 55 h after PMSG injection. For in vitro experiments, the mouse GCs obtained from healthy follicles were treated with CORT alone, or together with inhibitors against the glucocorticoid receptor (<i>Nr3c1</i>). The results showed that the CORT caused a downregulation of <i>Lhcgr</i> expression in GCs, which was accompanied by impaired cell viability. Moreover, the effect of the CORT was mediated by binding to its receptor (<i>Nr3c1</i>) in GCs. Further investigation revealed that <i>Nr3c1</i> might regulate the transcription of <i>Lhcgr</i> through inhibiting the expression of <i>Lhcgr</i> transcription factors, including AP1 and Creb. Taken together, our findings suggested a possible mechanism of CORT-induced anovulation involving the inhibition of <i>Lhcgr</i> expression in GCs by the CORT-<i>Nr3c1</i>-AP1/Creb axis."],"journal":["International journal of molecular sciences"],"pubmed_title":["The Corticosterone-Glucocorticoid Receptor-AP1/CREB Axis Inhibits the Luteinizing Hormone Receptor Expression in Mouse Granulosa Cells."],"pmcid":["PMC9604301"],"funding_grant_id":["DKQB201903","BK20221512","31601939","31972571","KJQN201705","31972564","31630072"],"pubmed_authors":["Li W","Shen M","Liu H","Li X","Liu Z","Li C","Zhang J","Zhang X","Cao Y","Zhang L","Wei Y"],"additional_accession":[]},"is_claimable":false,"name":"The Corticosterone-Glucocorticoid Receptor-AP1/CREB Axis Inhibits the Luteinizing Hormone Receptor Expression in Mouse Granulosa Cells.","description":"Under stress conditions, luteinizing hormone (LH)-mediated ovulation is inhibited, resulting in insufficient oocyte production and excretion during follicular development. When the body is stressed, a large amount of corticosterone (CORT) is generated, which will lead to a disorder of the body's endocrine system and damage to the body. Our previous work showed that CORT can block follicular development in mice. Since LH acts through binding with the luteinizing hormone receptor (<i>Lhcgr</i>), the present study aimed to investigate whether and how corticosterone (CORT) influences <i>Lhcgr</i> expression in mouse ovarian granulosa cells (GCs). For this purpose, three-week-old ICR female mice were injected intraperitoneally with pregnant mare serum gonadotropin (PMSG). In addition, the treatment group was injected with CORT (1 mg/mouse) at intervals of 8 h and the control group was injected with the same volume of methyl sulfoxide (DMSO). GCs were collected at 24 h, 48 h, and 55 h after PMSG injection. For in vitro experiments, the mouse GCs obtained from healthy follicles were treated with CORT alone, or together with inhibitors against the glucocorticoid receptor (<i>Nr3c1</i>). The results showed that the CORT caused a downregulation of <i>Lhcgr</i> expression in GCs, which was accompanied by impaired cell viability. Moreover, the effect of the CORT was mediated by binding to its receptor (<i>Nr3c1</i>) in GCs. Further investigation revealed that <i>Nr3c1</i> might regulate the transcription of <i>Lhcgr</i> through inhibiting the expression of <i>Lhcgr</i> transcription factors, including AP1 and Creb. Taken together, our findings suggested a possible mechanism of CORT-induced anovulation involving the inhibition of <i>Lhcgr</i> expression in GCs by the CORT-<i>Nr3c1</i>-AP1/Creb axis.","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Oct","modification":"2025-04-03T21:29:24.16Z","creation":"2025-04-03T21:29:24.16Z"},"accession":"S-EPMC9604301","cross_references":{"pubmed":["36293309"],"doi":["10.3390/ijms232012454"]}}