Dissecting the cell microenvironment of ovarian endometrioma through single-cell RNA sequencing

被引:0
|
作者
Jiangpeng Wu [1 ,2 ]
Siyu Xia [1 ]
Wenting Ye [1 ]
Yan Sun [1 ]
Jing Cai [1 ]
Fubing Yu [1 ]
Haiping Wen [1 ]
Xiuwei Yi [1 ]
Taikang Li [1 ]
Mingwei Chen [1 ]
Jiayun Chen [2 ,3 ]
Ge Song [4 ]
Chuanbin Yang [2 ]
Yali Song [1 ]
Jigang Wang [1 ,2 ,3 ,5 ]
机构
[1] Department of Reproductive Medicine,Dongguan Maternal and Child Health Care Hospital
[2] Department of Urology,and Shenzhen Clinical Research Centre for Geriatrics,Shenzhen People's Hospital,Southern University of Science and Technology
[3] State Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs,Artemisinin Research Center,and Institute of Chinese Materia Medica,China Academy of Chinese Medical Sciences
[4] Reproductive Medicine Center,Foshan Women and Children Hospital
[5] State Key Laboratory of Antiviral Drugs,School of Pharmacy,Henan
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中图分类号
R737.3 [女性生殖器肿瘤];
学科分类号
摘要
Ovarian endometrioma(OE), also known as “chocolate cysts,” is a cystic mass that develops in the ovaries due to endometriosis and is a common gynecological condition characterized by the growth of endometrial tissue outside the uterus, leading to symptoms such as dysmenorrhea, pelvic pain, and infertility. However, the precise molecular and cellular mechanisms driving this pathophysiology remain largely unknown, posing challenges for diagnosis and treatment. Here, we employed integrated single-cell transcriptomic profiling of over 52,000 individual cells from endometrial tissues of OE patients and healthy donors and identified twelve major cell populations. We identified notable alterations in cell type-specific proportions and molecular signatures associated with OE. Notably, the activation of IGFBP5+ macrophages with pro-inflammatory properties, NK cell exhaustion, and aberrant proliferation of IQCG+ and KLF2+ epithelium are key features and may be the potential mechanisms underlying the pathogenesis of OE. Collectively, our data contribute to a better understanding of OE at the single cell level and may pave the way for the development of novel therapeutic strategies.
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页码:116 / 129
页数:14
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