Decreased expression of caveolin-1 have relevance to promoted senescence in preeclamptic placenta

Pregnancy Hypertens. 2022 Dec:30:59-67. doi: 10.1016/j.preghy.2022.08.006. Epub 2022 Aug 9.

Abstract

Objectives: To assess the association between altered expression of caveolin-1 and p53/p21, as indicatives of cellular senescence, in preeclamptic placenta.

Study design: Placental tissues and serum were collected from rats (Sham and reduced uterine perfusion pressure group) at 18.5 days post coitum and humans (normotensive pregnant and preeclampsia groups). The concentration and expression of caveolin-1 were measured in the collected tissues, and the correlation between p53 and p21 expression was evaluation.

Main outcome measures: Placental mRNA expression and serum concentration of caveolin-1 were measured using qRT-PCR and ELISA, respectively. Altered expressions of caveolin-1 and p53/p21 were revealed and quantified by immunohistochemistry. The association between these changes was investigated using correlation analysis.

Results: Placental mRNA expressions and serum concentrations of caveolin-1 were significantly decreased in reduced uterine perfusion pressure and preeclampsia groups. The expressions of caveolin-1 and p53/ p21 were significantly altered in placenta complicated with preeclampsia. Correlation analysis revealed a significant inverse association between changes in caveolin-1 and p53/p21. Subsequently, these results were obtained by investigating the preeclampsia onset time.

Conclusion: These results revealed that the expression of caveolin-1 profoundly decreases in the placenta and serum of preeclampsia. These factors contribute to the mechanism of accelerated cellular senescence in placenta, which is one of the various etiologies of preeclampsia.

Keywords: Caveolin-1; Cellular senescence; Placenta; Placental aging; Preeclampsia.

MeSH terms

  • Animals
  • Case-Control Studies
  • Caveolin 1* / genetics
  • Caveolin 1* / metabolism
  • Female
  • Humans
  • Placenta* / metabolism
  • Pre-Eclampsia* / metabolism
  • Pregnancy
  • RNA, Messenger / metabolism
  • Rats
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • Caveolin 1
  • RNA, Messenger
  • Tumor Suppressor Protein p53
  • Cav1 protein, rat
  • CAV1 protein, human