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Original Research Article | OPEN ACCESS

USP22 promotes aspirin-induced trophoblast cell proliferation as well as migration via Wnt/β-catenin pathway in preeclampsia

Changcun Zhang, Qiping Han, E Luoji

Department of Obstetrics, Qinghai Provincial People's Hospital, Xining, Qinghai Province 810000, China;

For correspondence:-  E Luoji   Email: qipinghan_0509@163.com   Tel:+869718066165

Accepted: 1 May 2023        Published: 30 May 2023

Citation: Zhang C, Han Q, Luoji E. USP22 promotes aspirin-induced trophoblast cell proliferation as well as migration via Wnt/β-catenin pathway in preeclampsia. Trop J Pharm Res 2023; 22(5):987-992 doi: 10.4314/tjpr.v22i5.8

© 2023 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To investigate the involvement of ubiquitin-specific peptidase 22 (USP22) in the pathogenesis of preeclampsia (PE), and the potential mechanism of action.
Methods: To investigate the role of USP22 in preeclampsia, immunoblot assay as well as quantitative real-time polymerase chain reaction (qRT-PCR) were conducted to determine USP22 expression levels in placental tissues from both the control (non-preeclampsia normal) and the PE cases. Furthermore, cell counting kit-8 as well as EdU assays were performed to assess the impact of USP22 on the viability of HTR-8/Svneo and TEV-1 cells. Furthermore, wound closure and Transwell assays were used to examine the effect of USP22 on cell motility, while tube formation assay was used to determine the effect of USP22 on the angiogenesis of trophoblast cells. Finally, the effect of USP22 on Wnt/β-catenin pathway in HTR-8/Svneo and TEV-1 human trophoblast cells was evaluated by immunoblot analysis.
Results: USP22 expression was significantly reduced in PE placental tissue compared to control tissues. In addition, USP22 promoted trophoblast cell proliferation, increased cell motility as well as enhanced angiogenesis capacity. USP22 regulated the proliferation as well as migration of trophoblast cells via Wnt/β-catenin pathway. Notably, USP22 enhanced cell proliferation and migration in aspirin-induced PE.
Conclusion: USP22 plays a crucial role in inhibiting trophoblast cell growth by regulating Wnt/β-catenin pathway. Therefore, targeting USP22 may hold promise for the treatment of PE

Keywords: Preeclampsia, USP22, Proliferation, Angiogenesis, Trophoblast cells, Wnt/β-catenin pathway, Aspirin

Impact Factor
Thompson Reuters (ISI): 0.523 (2021)
H-5 index (Google Scholar): 39 (2021)

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