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异位基质细胞中差异表达的 miRNAs 促进子宫内膜异位症的发展:miR-139-5p 和 miR-375 的可能作用。

Differentially-Expressed miRNAs in Ectopic Stromal Cells Contribute to Endometriosis Development: The Plausible Role of miR-139-5p and miR-375.

机构信息

Department of Obstetrics and Gynecology, Institute of Clinical Medicine, University of Tartu, 50090 Tartu, Estonia.

Competence Centre on Health Technologies, 50410 Tartu, Estonia.

出版信息

Int J Mol Sci. 2018 Nov 28;19(12):3789. doi: 10.3390/ijms19123789.

Abstract

microRNA (miRNA) expression level alterations between endometrial tissue and endometriotic lesions indicate their involvement in endometriosis pathogenesis. However, as both endometrium and endometriotic lesions consist of different cell types in various proportions, it is not clear which cells contribute to variability in miRNA levels and the overall knowledge about cell-type specific miRNA expression in ectopic cells is scarce. Therefore, we utilized fluorescence-activated cell sorting to isolate endometrial stromal cells from paired endometrial and endometrioma biopsies and combined it with high-throughput sequencing to determine miRNA alterations in endometriotic stroma. The analysis revealed 149 abnormally expressed miRNAs in endometriotic lesions, including extensive upregulation of miR-139-5p and downregulation of miR-375 compared to eutopic cells. miRNA transfection experiments in the endometrial stromal cell line ST-T1b showed that the overexpression of miR-139-5p resulted in the downregulation of homeobox A9 () and expression, whereas the endothelin 1 () gene was regulated by miR-375. The results of this study provide further insights into the complex molecular mechanisms involved in endometriosis pathogenesis and demonstrate the necessity for cell-type-specific analysis of ectopic tissues to understand the interactions between different cell populations in disease onset and progression.

摘要

微小 RNA(miRNA)在子宫内膜组织和子宫内膜异位病变之间的表达水平改变表明它们参与了子宫内膜异位症的发病机制。然而,由于子宫内膜和子宫内膜异位病变都由不同比例的细胞类型组成,因此尚不清楚是哪些细胞导致了 miRNA 水平的变化,并且关于异位细胞中特定于细胞类型的 miRNA 表达的总体知识还很缺乏。因此,我们利用荧光激活细胞分选技术从配对的子宫内膜和子宫内膜瘤活检中分离子宫内膜基质细胞,并将其与高通量测序相结合,以确定子宫内膜异位症基质中的 miRNA 改变。分析显示,在子宫内膜异位病变中存在 149 个异常表达的 miRNA,与在位细胞相比,miR-139-5p 的表达显著上调,miR-375 的表达下调。在子宫内膜基质细胞系 ST-T1b 中的 miRNA 转染实验表明,miR-139-5p 的过表达导致同源盒 A9()和表达下调,而内皮素 1()基因受 miR-375 调控。这项研究的结果提供了对子宫内膜异位症发病机制中涉及的复杂分子机制的进一步了解,并表明有必要对异位组织进行特定于细胞类型的分析,以了解不同细胞群体在疾病发生和进展中的相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf63/6321240/2f5a5b2491dc/ijms-19-03789-g001.jpg

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