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瘦素通过 MTA1/WNT 和 PI3K/AKT 通路的串扰促进 HTR-8/SVneo 细胞侵袭。

Leptin Promotes HTR-8/SVneo Cell Invasion via the Crosstalk between MTA1/WNT and PI3K/AKT Pathways.

机构信息

Department of Obstetrics and Gynecology, The Second Hospital, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250033, China.

Department of Obstetrics and Gynecology, Qilu Hospital, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, China.

出版信息

Dis Markers. 2022 Nov 22;2022:7052176. doi: 10.1155/2022/7052176. eCollection 2022.

Abstract

The process of placental invasion is essential for a successful pregnancy. Leptin is involved in trophoblast invasiveness, and its dysregulation is connected with a series of diseases, including preeclampsia. However, the knowledge of the precise mechanisms in leptin-induced trophoblast invasiveness is still limited. According to the present research, transwell assay suggested that leptin is a dose- and time-dependent regulator in inducing HTR-8/SVneo cell invasion. Western blot analysis and immunofluorescence staining revealed that leptin-induced MMP9 expression is essential in the invasion process of HTR-8/SVneo cells. Mechanistically, we demonstrated that leptin activated -catenin via the crosstalk between the MTA1/WNT and PI3K/AKT pathways. Besides, we showed that downregulating the key molecules in the signaling pathways by siRNA can inhibit leptin-induced MMP9 expression and further suppress invasion of HTR-8/SVneo cells. In conclusion, our study revealed a new regulatory mechanism of leptin-induced HTR-8/SVneo cell invasiveness and will provide novel insights into the causes and potential therapeutic targets for diseases related to dysregulation of trophoblast invasion in the future.

摘要

胎盘侵入过程对于成功妊娠至关重要。瘦素参与滋养细胞的侵袭,其失调与一系列疾病有关,包括子痫前期。然而,瘦素诱导滋养细胞侵袭的确切机制的知识仍然有限。根据目前的研究,Transwell 分析表明,瘦素是诱导 HTR-8/SVneo 细胞侵袭的一种剂量和时间依赖性调节剂。Western blot 分析和免疫荧光染色显示,瘦素诱导的 MMP9 表达在 HTR-8/SVneo 细胞的侵袭过程中是必不可少的。从机制上讲,我们证明瘦素通过 MTA1/WNT 和 PI3K/AKT 通路的串扰激活了-catenin。此外,我们还表明,通过 siRNA 下调信号通路中的关键分子可以抑制瘦素诱导的 MMP9 表达,并进一步抑制 HTR-8/SVneo 细胞的侵袭。总之,我们的研究揭示了瘦素诱导 HTR-8/SVneo 细胞侵袭的新调节机制,为未来与滋养细胞侵袭失调相关疾病的病因和潜在治疗靶点提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bef4/9708374/173e28c8cc25/DM2022-7052176.001.jpg

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