Down-regulation of TAGLN2 associated with the development of preeclampsia by effecting the Rap1 signaling pathway.

Placenta

Department of Obstetrics and Gynaecology, Peking University Shenzhen Hospital, Shenzhen Peking University-The Hong Kong University of Science and Technology Medical Center, Shenzhen, Guangdong, China; Department of Obstetrics and Gynaecology, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China; Shenzhen Key Laboratory on Technology for Early Diagnosis of Major Gynecological Diseases, Shenzhen, China. Electronic address:

Published: November 2024

AI Article Synopsis

  • Preeclampsia (PE) is a serious condition affecting pregnancy health, with limited treatment options, prompting research into new therapies targeting the role of Transgelin-2 (TAGLN2) and the Rap1 signaling pathway.
  • This study used placentas from PE patients and created models by down-regulating TAGLN2 in mice and cell lines to analyze how its suppression affects PE development through molecular mechanisms.
  • The results showed that down-regulation of TAGLN2 decreases the expression of Rap1A, hindering cell proliferation and migration in trophoblasts, thereby suggesting that TAGLN2’s role is significant in PE progression via the inhibition of the Rap1 signaling pathway.

Article Abstract

Introduction: Preeclampsia (PE) poses significant global challenges to pregnancy health, being a leading cause of maternal and perinatal morbidity and mortality. Unfortunately, effective treatment options remain limited, necessitating the urgent development of novel therapeutic strategies. This study is to investigate down-regulation of Transgelin-2 (TAGLN2) contributes to the development of PE through suppression of the Rap1 signaling pathway.

Methods: Placentas from PE patients were collected for a transcriptome analysis. Down-regulation experiments of TAGLN2 were performed in mouse and HTR-8/SVneo cells to generate PE models. The mechanism by which down-regulation of TAGLN2 induces PE was explored based on these PE model through transcriptome and proteome analysis and molecular tests.

Results: Our findings revealed that the expression levels of Rap1A was significantly reduced in the placenta of PE patients. The expression level of Rap1A in the placental tissue of sh_Tagln2 PE model mice is down-regulated. In addition, TAGLN2 down-regulation impede the proliferation and migration of HTR8/SVneo cells and lead to the decreased expression of Rap1A. Meanwhile, Rap1A down-regulation impede both the proliferation and migration of HTR8/SVneo cells. Both transcriptomic and proteomic levels of sh-TG2 HTR8/Svneo cells demonstrated Rap1 signaling pathway and related key genes was inhibited after TAGLN2 down-regulation.

Conclusion: Our results confirm that down-regulation of TAGLN2 in HTR-8/SVneo cells leads to the decreased Rap1A expression and suppresses trophoblast cell proliferation and migration by inhibiting Rap1 signaling pathway. Meanwhile, Rap1A down-regulation impede both the proliferation and migration of HTR8/SVneo cells. These findings concluded that down-regulation of TAGLN2 may be implicated in the development of preeclampsia through its effect on the Rap1 signaling pathway.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.placenta.2024.11.009DOI Listing

Publication Analysis

Top Keywords

rap1 signaling
20
down-regulation tagln2
16
signaling pathway
16
proliferation migration
16
htr8/svneo cells
16
down-regulation impede
12
impede proliferation
12
migration htr8/svneo
12
down-regulation
9
development preeclampsia
8

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!