单细胞RNA测序揭示局部肾素-血管紧张素系统在调节卵巢生理周期和促进PCOS中的作用。

IF 6.1 2区 生物学 Q1 CELL BIOLOGY
Lun Wei, Le Bo, Wangtao Jiang, Ruofan Qi, Chao Luo, Fei Qian, Panjie Ma, Jianping Qiu, Caiping Mao
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引用次数: 0

摘要

卵巢中存在局部肾素-血管紧张素系统(RAS),参与调节许多重要的生理过程,但具体机制尚不清楚。多囊卵巢综合征(PCOS)是最常报道的RAS表达异常的非医源性疾病,以超重或肥胖和胰岛素抵抗(IR)为特征,两者都与许多长期并发症显著相关。这些疾病与循环或局部RAS密切相关,作为潜在的共同调节节点。本研究通过对小鼠生殖期卵巢单细胞RNA测序(scRNA-seq)数据进行分析,获得RAS组分在各细胞簇中的表达水平和位置信息。进一步分析了RAS在发情周期中的周期性波动和差异基因集。蛋白-蛋白相互作用分析预测了与RAS相互作用最密切的途径,并在scRNA-seq数据中发现了血管紧张素II (AngII)与胰岛素信号通路之间串扰的初步证据。构建PCOS小鼠模型,复制临床生殖和代谢并发症,并验证AngII与IRS1/PI3K/AKT之间的串扰。综上所述,本研究揭示了卵巢局部RAS在发情周期细胞水平上的动态变化,并从单细胞角度阐述了RAS在调节卵巢功能中的作用。这也证明了由AngII和IRS1/PI3K/AKT通路之间的串扰引起的IR可能是PCOS的潜在机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Single cell RNA sequencing reveals the role of local renin-angiotensin system in regulating ovarian physiological cycle and promoting PCOS.

There is a local renin-angiotensin system (RAS) in the ovary, which is involved in regulating many important physiological processes, but the specific mechanism remains unclear. Polycystic ovarian syndrome (PCOS) is the most frequently reported non-iatrogenic condition with abnormal RAS expression, characterized by overweight or obesity and insulin resistance (IR), both of which are significantly correlated with many long-term complications. These conditions are closely linked to circulatory or local RAS, serving as potential common regulatory nodes. The present study analyzed single-cell RNA sequencing (scRNA-seq) data from mouse ovaries during the reproductive period to obtain the expression levels and location information of RAS components in all cell clusters. It further analyzed the cyclical fluctuations of RAS and the differential gene sets during the estrous cycle. Protein-protein interaction analysis predicted the most closely interacting pathway with RAS, and preliminary evidence of crosstalk between angiotensin II (AngII) and the insulin signaling pathway was identified in the scRNA-seq data. A PCOS mouse model was constructed, replicating clinical reproductive and metabolic complications, and the crosstalk between AngII and IRS1/PI3K/AKT was verified. In conclusion, this study revealed the dynamic changes of the ovarian local RAS at the cellular level during the estrous cycle, and described the role of RAS in regulating ovarian function from a single-cell perspective. It also provided evidence that IR, caused by the crosstalk between AngII and IRS1/PI3K/AKT pathways, may be a potential underlying mechanism of PCOS.

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来源期刊
Cell Death Discovery
Cell Death Discovery Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
8.30
自引率
1.40%
发文量
468
审稿时长
9 weeks
期刊介绍: Cell Death Discovery is a multidisciplinary, international, online-only, open access journal, dedicated to publishing research at the intersection of medicine with biochemistry, pharmacology, immunology, cell biology and cell death, provided it is scientifically sound. The unrestricted access to research findings in Cell Death Discovery will foster a dynamic and highly productive dialogue between basic scientists and clinicians, as well as researchers in industry with a focus on cancer, neurobiology and inflammation research. As an official journal of the Cell Death Differentiation Association (ADMC), Cell Death Discovery will build upon the success of Cell Death & Differentiation and Cell Death & Disease in publishing important peer-reviewed original research, timely reviews and editorial commentary. Cell Death Discovery is committed to increasing the reproducibility of research. To this end, in conjunction with its sister journals Cell Death & Differentiation and Cell Death & Disease, Cell Death Discovery provides a unique forum for scientists as well as clinicians and members of the pharmaceutical and biotechnical industry. It is committed to the rapid publication of high quality original papers that relate to these subjects, together with topical, usually solicited, reviews, editorial correspondence and occasional commentaries on controversial and scientifically informative issues.
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