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白细胞介素-17 通过调节过氧化物酶体增殖物激活受体-γ/视黄醇 X 受体-α/β-连环蛋白信号通路促进滋养细胞的增殖、迁移和侵袭。

Interleukin-17 promotes proliferation, migration, and invasion of trophoblasts via regulating PPAR-γ/RXR-α/Wnt signaling.

机构信息

Department of Pathology, Shijiazhuang People's Hospital, Shijiazhuang City, Hebei Province, China.

出版信息

Bioengineered. 2022 Jan;13(1):1224-1234. doi: 10.1080/21655979.2021.2020468.

Abstract

To investigate the effect of Interleukin 17 (IL-17) on the invasive capacity of trophoblast cells and the underlying mechanism, we collected placental tissues samples from pregnant women with preeclampsia (PE) and healthy pregnant women. The expression levels of IL-17 mRNA and protein in tissue samples were determined using qRT-PCR and Western blot, respectively. Cell viability and cell proliferation was determined using CCK-8 assay, and colony formation assay, respectively. Cell migration and invasion capacity were determined using transwell cell migration assay. Our results showed that the mRNA expression of IL-17 was significantly increased in PE patients and may be used as a sensitive biomarker for PE ( < 0.01). IL-17 overexpression promoted cell viability, migration, and invasion of human extravillous trophoblast cell line, HTR8/SVneo; however, IL-17 knockdown inhibited these effects. Additionally, IL-17 activated PPAR-γ/RXR-α signaling pathway, which promoted proliferation, migration, and invasion of trophoblast cells. Moreover, PPAR-γ/RXR-α heterodimers activated Wnt signaling. In conclusion, our study provides evidence that IL-17 is overexpressed in PE and promotes proliferation, migration and invasion of trophoblast cells via activating PPAR-γ/RXR-α/Wnt signaling.

摘要

为了研究白细胞介素 17(IL-17)对滋养层细胞侵袭能力的影响及其潜在机制,我们收集了子痫前期(PE)孕妇和健康孕妇的胎盘组织样本。使用 qRT-PCR 和 Western blot 分别检测组织样本中 IL-17 mRNA 和蛋白的表达水平。使用 CCK-8 测定法和集落形成测定法分别测定细胞活力和细胞增殖。使用 Transwell 细胞迁移测定法测定细胞迁移和侵袭能力。我们的结果表明,IL-17 的 mRNA 表达在 PE 患者中显著增加,可能作为 PE 的敏感生物标志物(<0.01)。IL-17 过表达促进人绒毛外滋养层细胞系 HTR8/SVneo 的细胞活力、迁移和侵袭;然而,IL-17 敲低抑制了这些效应。此外,IL-17 激活了 PPAR-γ/RXR-α 信号通路,促进了滋养层细胞的增殖、迁移和侵袭。此外,PPAR-γ/RXR-α 异二聚体激活了 Wnt 信号。总之,我们的研究提供了证据表明,IL-17 在 PE 中过度表达,并通过激活 PPAR-γ/RXR-α/Wnt 信号促进滋养层细胞的增殖、迁移和侵袭。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf21/8805847/1bc66f2935cb/KBIE_A_2020468_F0001_OC.jpg

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