Circ_0090100 induces AHNAK expression to inhibit trophoblast cell proliferation and invasion and accelerate cell apoptosis by segregating miR-139-5p in preeclampsia.

IF 3.4 3区 生物学 Q3 CELL BIOLOGY
Zhenli Shan, Linfang Zhou, Yan Ma, Yiying Huang
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Abstract

The etiology of preeclampsia (PE) is complex and is known to involve the expression of circular RNAs (circRNAs). Among these, the function of circ_0090100 in PE is yet to be fully understood. This study was conducted to examine the expression profile of circ_0090100 in placental tissues from PE patients and to assess its influence on trophoblast cell functions. Quantitative real-time polymerase chain reaction (qRT-PCR) was used to measure the RNA expression levels of circ_0090100, microRNA-139-5p (miR-139-5p), and AHNAK nucleoprotein (AHNAK). Cell viability, proliferation, apoptosis, and invasion were assessed using the CCK-8 assay, EdU incorporation, flow cytometry, and transwell migration assays, respectively. Western blot analysis was performed to detect the protein expression of N-cadherin, Vimentin, and AHNAK. Dualluciferase reporter assay and RNA immunoprecipitation (RIP) assay were conducted to elucidate the relationships between circ_0090100, miR-139-5p, and AHNAK. We found that the expression of circ_0090100 and AHNAK was upregulated, while miR-139-5p. expression was downregulated in PE placental tissues compared to controls. Transfection of a plasmid overexpressing circ_0090100 into JEG-3 and HTR-8/SVneo trophoblast cell lines resulted in reduced cell proliferation and invasion, but increased apoptosis. Mechanistically, circ_0090100 functioned as a miR-139-5p sponge, and miR-139-5p targeted AHNAK. Furthermore, upregulating miR-139-5p reversed the effects of circ_0090100 in JEG-3 and HTR-8/SVneo cells. AHNAK was found to be involved in the regulation of miR-139-5p effects on trophoblast cells. Additionally, circ_0090100 induced the production of AHNAK through miR-139-5p. Therefore, circ_0090100 activated AHNAK to suppress trophoblast cell proliferation and invasion, and promote cell apoptosis, via miR-139-5p.

Circ_0090100通过分离miR-139-5p诱导AHNAK表达抑制滋养细胞增殖和侵袭,加速子痫前期细胞凋亡。
子痫前期(PE)的病因复杂,已知与环状rna (circRNAs)的表达有关。其中,circ_0090100在PE中的作用尚未完全了解。本研究旨在检测circ_0090100在PE患者胎盘组织中的表达谱,并评估其对滋养细胞功能的影响。采用实时定量聚合酶链反应(qRT-PCR)检测circ_0090100、microRNA-139-5p (miR-139-5p)和AHNAK核蛋白(AHNAK)的RNA表达水平。分别采用CCK-8法、EdU掺入法、流式细胞术和transwell迁移法评估细胞活力、增殖、凋亡和侵袭。Western blot检测N-cadherin、Vimentin、AHNAK蛋白的表达。为了阐明circ_0090100、miR-139-5p和AHNAK之间的关系,我们进行了双荧光素酶报告基因测定和RNA免疫沉淀(RIP)测定。我们发现circ_0090100和AHNAK的表达上调,而miR-139-5p。与对照组相比,PE胎盘组织中的表达下调。将过表达circ_0090100的质粒转染到JEG-3和HTR-8/SVneo滋养细胞中,细胞增殖和侵袭减少,但凋亡增加。在机制上,circ_0090100作为miR-139-5p海绵,miR-139-5p靶向AHNAK。此外,上调miR-139-5p可逆转circ_0090100在JEG-3和HTR-8/SVneo细胞中的作用。AHNAK被发现参与miR-139-5p对滋养细胞作用的调控。此外,circ_0090100通过miR-139-5p诱导AHNAK的产生。因此,circ_0090100通过miR-139-5p激活AHNAK抑制滋养细胞增殖和侵袭,促进细胞凋亡。
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来源期刊
Human Cell
Human Cell CELL BIOLOGY-
CiteScore
5.90
自引率
2.30%
发文量
176
审稿时长
4.5 months
期刊介绍: Human Cell is the official English-language journal of the Japan Human Cell Society. The journal serves as a forum for international research on all aspects of the human cell, encompassing not only cell biology but also pathology, cytology, and oncology, including clinical oncology. Embryonic stem cells derived from animals, regenerative medicine using animal cells, and experimental animal models with implications for human diseases are covered as well. Submissions in any of the following categories will be considered: Research Articles, Cell Lines, Rapid Communications, Reviews, and Letters to the Editor. A brief clinical case report focusing on cellular responses to pathological insults in human studies may also be submitted as a Letter to the Editor in a concise and short format. Not only basic scientists but also gynecologists, oncologists, and other clinical scientists are welcome to submit work expressing new ideas or research using human cells.
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