State Key Laboratory of Female Fertility Promotion, Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, Beijing, China.
National Clinical Research Center for Obstetrics and Gynecology (Peking University Third Hospital), Beijing, China.
Reprod Biol Endocrinol. 2024 Aug 6;22(1):98. doi: 10.1186/s12958-024-01269-9.
At present, a number of clinical trials have been carried out on GLP-1 receptor agonist liraglutide in the treatment of polycystic ovary syndrome (PCOS). However, the effect of liraglutide on follicle development and its specific mechanism are still unclear.
RNA sequencing was used to explore the molecular characteristics of granulosa cells from patients with PCOS treated with liraglutide. The levels of C-X-C motif chemokine ligand 10 (CXCL10) in follicular fluid were detected by ELISA, the expression levels of ovulation related genes and inflammatory factor genes in follicles and granulosa cells were detected by qPCR and the protein levels of connexin 43 (Cx43), Janus Kinase 2 (JAK2) and phosphorylated JAK2 were detected by Western blot. The mouse ovarian follicles culture system in vitro was used to detect the status of follicle development and ovulation.
In the present study, we found that liraglutide inhibited the secretion of inflammatory factors in PCOS granulosa cells, among which CXCL10 was the most significant. In addition, CXCL10 was significantly higher in granulosa cells and follicular fluid in PCOS patients than in non-PCOS patients. We applied in vitro follicle culture and other techniques to carry out the mechanism exploration which revealed that CXCL10 disrupted the homeostasis of gap junction protein alpha 1 (GJA1) between oocyte and granulosa cells before physiological ovulation, thus inhibiting follicular development and ovulation. Liraglutide inhibited CXCL10 secretion in PCOS granulosa cells by inhibiting the JAK signaling pathway and can improved dehydroepiandrosterone (DHEA)-induced follicle development disorders, which is reversed by CXCL10 supplementation.
The present study suggests that liraglutide inhibits CXCL10 secretion in granulosa cells through JAK signaling pathway, thereby improving the homeostasis of GJA1 between oocyte and granulosa cells before physiological ovulation and ultimately improving the follicular development and ovulation of PCOS, which provides more supportive evidence for the clinical application of liraglutide in the treatment of ovulatory disorders in PCOS.
Not applicable.
目前,已有多项关于 GLP-1 受体激动剂利拉鲁肽治疗多囊卵巢综合征(PCOS)的临床试验。然而,利拉鲁肽对卵泡发育的影响及其具体机制尚不清楚。
采用 RNA 测序技术探讨利拉鲁肽治疗的 PCOS 患者颗粒细胞的分子特征。采用 ELISA 法检测卵泡液中趋化因子配体 10(CXCL10)水平,qPCR 检测卵泡和颗粒细胞中排卵相关基因和炎症因子基因的表达水平,Western blot 检测连接蛋白 43(Cx43)、Janus 激酶 2(JAK2)和磷酸化 JAK2 的蛋白水平。采用体外小鼠卵巢卵泡培养系统检测卵泡发育和排卵状态。
本研究发现,利拉鲁肽抑制 PCOS 颗粒细胞中炎症因子的分泌,其中 CXCL10 最为显著。此外,PCOS 患者的颗粒细胞和卵泡液中 CXCL10 明显高于非 PCOS 患者。我们应用体外卵泡培养等技术进行机制探讨,结果表明,CXCL10 在生理排卵前破坏卵母细胞和颗粒细胞之间的间隙连接蛋白 alpha 1(GJA1)的内环境平衡,从而抑制卵泡发育和排卵。利拉鲁肽通过抑制 JAK 信号通路抑制 PCOS 颗粒细胞中 CXCL10 的分泌,可改善脱氢表雄酮(DHEA)诱导的卵泡发育障碍,该作用可被 CXCL10 补充所逆转。
本研究表明,利拉鲁肽通过 JAK 信号通路抑制颗粒细胞中 CXCL10 的分泌,从而改善生理排卵前卵母细胞和颗粒细胞之间 GJA1 的内环境平衡,最终改善 PCOS 的卵泡发育和排卵,为利拉鲁肽治疗 PCOS 排卵障碍的临床应用提供了更多支持证据。
不适用。