多囊卵巢综合征妇女的止血动力学改变及其对卵泡微环境的调节。

IF 3
Roshan Dadachanji, Snehal Bhingardeve, Sadhana K Desai, Vijay Mangoli, Srabani Mukherjee
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引用次数: 0

摘要

多囊卵巢综合征(PCOS),表现为妇科和代谢问题,如无排卵性不孕、胰岛素抵抗、高雄激素症和肥胖,以及长期的心脏代谢风险。新出现的证据表明,凝血-纤溶平衡影响卵巢基本功能,包括排卵、黄体功能、颗粒细胞黄体化和ECM重塑。本研究探讨了印度女性卵巢微环境中相对未被充分研究的凝血和纤溶因子。本病例对照研究通过分析卵泡液(FF)和颗粒细胞(GCs)中的凝血和纤维蛋白溶解谱,检测了PCOS患者(35例)和对照组(30例)的卵泡微环境的止血潜能。我们观察到丝氨酸蛋白酶抑制剂(SERPINE1)、组织型纤溶酶原激活剂(PLAT)、凝血因子纤维蛋白原γ (FGG)等纤维蛋白溶解因子在PCOS GCs中的转录表达显著降低。相反,血栓调节素(THBD)和尿激酶纤溶酶原激活物受体(PLAUR)的转录水平在PCOS女性的GCs中显著高于对照组。PCOS女性FF中纤溶酶原激活剂PLAT和PLAU水平以及抗凝蛋白、组织因子途径抑制剂和蛋白S水平均明显下降,而纤溶酶原、THBD和富组氨酸糖蛋白水平显著升高。此外,miRNA-mRNA调控网络的构建提示mirna也可能参与PCOS卵泡微环境的止血调节。我们的研究表明,多囊卵巢综合征的卵泡微环境中凝血和纤溶因子的改变可能导致止血平衡被破坏,主要表现为纤维蛋白溶解功能受损。这可能对受影响妇女因破裂改变、ECM重塑和积云扩张而导致的排卵功能障碍具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Altered hemostatic dynamics and its regulation in follicular microenvironment of women with polycystic ovary syndrome.

Polycystic ovary syndrome (PCOS), presents with gynecological and metabolic issues such as anovulatory infertility, insulin resistance, hyperandrogenism, and obesity, and long-term cardiometabolic risks. Emerging evidence highlights coagulation-fibrinolysis balance influences essential ovarian functions, including ovulation, corpus luteum function, granulosa cell luteinization, and ECM remodeling. This study explores the relatively understudied coagulation and fibrinolytic factors in the ovarian microenvironment in Indian women. This case-control study examined the hemostatic potential of the follicular microenvironment in PCOS (n = 35) and controls (n = 30) by analyzing coagulation and fibrinolytic profiles in follicular fluid (FF), and granulosa cells (GCs). We observed significantly reduced transcript expressions of fibrinolytic factors including serine proteinase inhibitor (SERPINE1), tissue-type plasminogen activator (PLAT), coagulation factor fibrinogen gamma (FGG) in PCOS GCs. Conversely, transcript levels of thrombomodulin (THBD) and urokinase plasminogen activator receptor (PLAUR) were significantly higher in GCs of PCOS women compared to controls. Levels of both plasminogen activators, PLAT and PLAU, along with anticoagulant proteins, tissue factor pathway inhibitor and protein S were markedly declined, while plasminogen, THBD and histidine rich glycoprotein levels were significantly raised in FF of women with PCOS. Further, the construction of miRNA-mRNA regulatory network suggested that miRNAs may also be involved in hemostatic regulation in follicle microenvironment of PCOS. Our study showed that altered profiles of coagulation and fibrinolysis factors within follicular microenvironment of PCOS could contribute to disrupted hemostatic balance, mainly evidenced by compromised fibrinolysis. This may have significant implications for ovulatory dysfunction due to altered rupture, ECM remodeling and cumulus expansion in affected women.

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