Human Seminal Extracellular Vesicles Enhance Endometrial Receptivity Through Leukemia Inhibitory Factor.

IF 3.8 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Hanshu Wang, Yu Lin, Rongrong Chen, Yu Zhu, Hongqiang Wang, Shengxian Li, Lei Yu, Kaishu Zhang, Yujie Liu, Tao Jing, Fei Sun
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引用次数: 0

Abstract

Seminal extracellular vesicles (EVs) contain different subgroups that have diverse effects on sperm function. However, the effect of seminal EVs-especially their subgroups-on endometrial receptivity is largely unknown. Here, we found that seminal EVs could be divided into high-density EVs (EV-H), medium density EVs, and low-density EVs after purification using iodixanol. We demonstrated that EV-H could promote the expression and secretion of leukemia inhibitor factor (LIF) in human endometrial cells. In EV-H-treated endometrial cells, we identified 1274 differentially expressed genes (DEGs). DEGs were enriched in cell adhesion and AKT and STAT3 pathways. Therefore, we illustrated that EV-H enhanced the adhesion of human choriocarcinoma JAr cell spheroids to endometrial cells through the LIF-STAT3 pathway. Collectively, our findings indicated that seminal EV-H could regulate endometrial receptivity through the LIF pathway, which could provide novel insights into male fertility.

人类精液细胞外囊泡通过白血病抑制因子增强子宫内膜的接受能力
精液细胞外囊泡(EVs)含有不同的亚群,它们对精子的功能有不同的影响。然而,精液EVs(尤其是其亚群)对子宫内膜受孕率的影响却鲜为人知。在这里,我们发现精液 EVs 经碘桑醇纯化后可分为高密度 EV(EV-H)、中密度 EV(EV-M)和低密度 EV(EV-L)。然后,我们证明了 EV-H 能促进人子宫内膜细胞中白血病抑制因子(LIF)的表达和分泌。在 EV-H 处理过的子宫内膜细胞中,我们发现了 1274 个差异表达基因(DEGs)。DEGs富集于细胞粘附和AKT、STAT3通路。因此,我们表明,EV-H 通过 LIF-STAT3 通路增强了人绒毛膜癌 JAr 细胞球与子宫内膜细胞的粘附。总之,我们的研究结果表明,精液 EV-H 可通过 LIF 通路调节子宫内膜的接受能力,这将为男性生育提供新的见解。
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来源期刊
Endocrinology
Endocrinology 医学-内分泌学与代谢
CiteScore
8.10
自引率
4.20%
发文量
195
审稿时长
2-3 weeks
期刊介绍: The mission of Endocrinology is to be the authoritative source of emerging hormone science and to disseminate that new knowledge to scientists, clinicians, and the public in a way that will enable "hormone science to health." Endocrinology welcomes the submission of original research investigating endocrine systems and diseases at all levels of biological organization, incorporating molecular mechanistic studies, such as hormone-receptor interactions, in all areas of endocrinology, as well as cross-disciplinary and integrative studies. The editors of Endocrinology encourage the submission of research in emerging areas not traditionally recognized as endocrinology or metabolism in addition to the following traditionally recognized fields: Adrenal; Bone Health and Osteoporosis; Cardiovascular Endocrinology; Diabetes; Endocrine-Disrupting Chemicals; Endocrine Neoplasia and Cancer; Growth; Neuroendocrinology; Nuclear Receptors and Their Ligands; Obesity; Reproductive Endocrinology; Signaling Pathways; and Thyroid.
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