Role of SAA1 in endometrial extracellular matrix remodeling in polycystic ovary syndrome: implication for pregnancy loss.

IF 5 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Journal of Clinical Endocrinology & Metabolism Pub Date : 2024-08-30 DOI:10.1210/clinem/dgae596
Qinling Zhu, Yuan Wang, Lizhen Xu, Mengjia Shi, Yiwen Meng, Congwen Shao, Yao Lu, Yaqiong He, Jiaan Huang, Xinyu Li, Boyu Li, Yijing Long, Ying Ding, Jia Qi, Wangsheng Wang, Yanzhi Du, Yun Sun
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Abstract

Context: Abnormal endometrial extracellular matrix (ECM) remodeling compromises endometrial receptivity and diminishes the probability of a successful live birth. Serum amyloid A1 (SAA1), a modulator of inflammation, is elevated in the circulation of polycystic ovary syndrome (PCOS) patients and involved in ECM remodeling during tissue repair. However, the specific role of SAA1 in endometrial ECM remodeling and subsequent risk of pregnancy loss in PCOS patients remains unclear.

Objective: To examine the role and underlying mechanism of SAA1 in ECM remodeling in the endometrium of PCOS patients.

Design: Serum samples from PCOS and control patients were utilized to investigate the relationship between the abundance of SAA1 and pregnancy loss. Human endometrial tissues and primary human endometrial stromal cells were used to examine the role and underlying mechanism of SAA1 in ECM remodeling.

Results: Serum SAA1 concentration was elevated and could serve as an independent risk of pregnancy loss in PCOS patients. Increased SAA1 abundance was also observed in endometrium obtained from these patients. Further mechanistic studies showed that SAA1 stimulated collagen I chains synthesis (COL1A1 and COL1A2) in endometrial stromal cells, suggesting excessive SAA1 may contribute to endometrial ECM remodeling, resulting in a non-supportive environment for ongoing pregnancy. This effect was abolished by either a toll-like receptors 2/4 antagonist or a nuclear factor κB inhibitor.

Conclusions: The locally elevated levels of SAA1 in endometrium contribute to ECM over-deposition by inducing collagen I synthesis in PCOS patients, which may hamper embryo implantation and increase the risk of pregnancy loss. These observations highlight the crucial role of heightened SAA1 in orchestrating endometrial dysfunction and shed light on potential therapeutic avenues for improving reproductive outcomes in PCOS patients.

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SAA1 在多囊卵巢综合征子宫内膜细胞外基质重塑中的作用:对妊娠失败的影响。
背景:子宫内膜细胞外基质(ECM)重塑异常会损害子宫内膜的接受能力,降低成功活产的概率。血清淀粉样蛋白 A1(SAA1)是炎症的调节剂,在多囊卵巢综合征(PCOS)患者的血液循环中升高,并参与组织修复过程中的 ECM 重塑。然而,SAA1 在多囊卵巢综合征患者子宫内膜 ECM 重塑和随后的妊娠失败风险中的具体作用仍不清楚:研究 SAA1 在多囊卵巢综合征患者子宫内膜 ECM 重塑中的作用及其内在机制:设计:利用多囊卵巢综合征患者和对照组患者的血清样本研究 SAA1 丰度与妊娠失败之间的关系。利用人类子宫内膜组织和原代人类子宫内膜基质细胞研究 SAA1 在 ECM 重塑中的作用和潜在机制:结果:血清 SAA1 浓度升高,可能是多囊卵巢综合征患者妊娠失败的独立风险因素。在这些患者的子宫内膜中也观察到 SAA1 丰度增加。进一步的机理研究表明,SAA1 可刺激子宫内膜基质细胞中胶原 I 链(COL1A1 和 COL1A2)的合成,这表明过量的 SAA1 可能会导致子宫内膜 ECM 重塑,从而造成不利于持续妊娠的环境。收费样受体2/4拮抗剂或核因子κB抑制剂均可消除这种效应:结论:多囊卵巢综合征患者子宫内膜中局部升高的 SAA1 水平通过诱导胶原 I 的合成导致 ECM 过度沉积,这可能会阻碍胚胎着床并增加妊娠失败的风险。这些观察结果凸显了 SAA1 水平升高在协调子宫内膜功能障碍中的关键作用,并为改善多囊卵巢综合症患者的生殖预后提供了潜在的治疗途径。
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来源期刊
Journal of Clinical Endocrinology & Metabolism
Journal of Clinical Endocrinology & Metabolism 医学-内分泌学与代谢
CiteScore
11.40
自引率
5.20%
发文量
673
审稿时长
1 months
期刊介绍: The Journal of Clinical Endocrinology & Metabolism is the world"s leading peer-reviewed journal for endocrine clinical research and cutting edge clinical practice reviews. Each issue provides the latest in-depth coverage of new developments enhancing our understanding, diagnosis and treatment of endocrine and metabolic disorders. Regular features of special interest to endocrine consultants include clinical trials, clinical reviews, clinical practice guidelines, case seminars, and controversies in clinical endocrinology, as well as original reports of the most important advances in patient-oriented endocrine and metabolic research. According to the latest Thomson Reuters Journal Citation Report, JCE&M articles were cited 64,185 times in 2008.
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