Han Ying, Diao Junrong, Wang Xinyan, Zhang Shuai, Yuan Lina, Ping Yaqiong, Zhang Yunshan, Luo Haining
Tianjin Central Hospital of Obstetrics and Gynecology/Nankai University Affiliated Maternity Hospital, Tianjin Key Laboratory of Human Development and Reproductive Regulation, Tianjin, 300100, People's Republic of China.
J Inflamm Res. 2024 Dec 18;17:11221-11234. doi: 10.2147/JIR.S490996. eCollection 2024.
To investigate the follicle microenvironments of women with premature ovarian insufficiency (POI), with normal ovarian reserve function, and who are older (age >40 years) and to identify potential therapeutic targets.
In total, 9 women who underwent in vitro fertilization(IVF) or intracytoplasmic sperm injection(ICSI) were included in this study. The first punctured follicle of each patient was used. Single-cell RNA sequencing was subsequently performed to explore the characteristics of the follicle microenvironments of women with POI, with a normal ovarian reserve and who were older.
In total, 87,323 cells were isolated and grouped into six clusters: T cells, B cells, neutrophils, basophils, mononuclear phagocytes (MPs), and granulosa cells. The study demonstrated that the POI samples had a smaller component ratio of MPs than did the other samples. The correlation between MPs and granulosa cells may lead to the development of POI. We found that the gene that was simultaneously downregulated in the POI group compared with the normal and older age groups was HLA-DRB5. Moreover, we observed that HLA-DRB5 was expressed mainly in monocytes. The temporal differentiation trajectory revealed that different monocytes play important roles in the beginning and end stages of differentiation. The C5AR1 gene is highly expressed in monocytes.
Our findings revealed that the interaction between monocytes and granulocytes may contribute to the development of POI. We found that POI lacked HLA-DRB5 expression and had impaired antigen processing and presentation activities. To a certain extent, C5AR1 could be used to predict the development of POI.
研究卵巢早衰(POI)女性、卵巢储备功能正常女性以及年龄较大(年龄>40岁)女性的卵泡微环境,并确定潜在的治疗靶点。
本研究共纳入9例行体外受精(IVF)或卵胞浆内单精子注射(ICSI)的女性。使用每位患者的首个穿刺卵泡。随后进行单细胞RNA测序,以探索POI女性、卵巢储备功能正常女性以及年龄较大女性的卵泡微环境特征。
共分离出87323个细胞,分为六个簇:T细胞、B细胞、中性粒细胞、嗜碱性粒细胞、单核吞噬细胞(MPs)和颗粒细胞。研究表明,POI样本中MPs的组成比例低于其他样本。MPs与颗粒细胞之间的相关性可能导致POI的发生。我们发现,与正常年龄组和年龄较大组相比,POI组中同时下调的基因是HLA-DRB5。此外,我们观察到HLA-DRB5主要在单核细胞中表达。时间分化轨迹显示,不同的单核细胞在分化的起始和终末阶段发挥重要作用。C5AR1基因在单核细胞中高表达。
我们的研究结果表明,单核细胞与粒细胞之间的相互作用可能促成POI的发生。我们发现POI缺乏HLA-DRB5表达,且抗原加工和呈递活性受损。在一定程度上,C5AR1可用于预测POI的发生。