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Transcriptomic Profiling of JEG-3 cells using human leiomyoma derived matrix

  • Samineh Barmaki*
  • , Ahmed Al-Samadi
  • , Katarzyna Leskinen
  • , Wafa Wahbi
  • , Ville Jokinen
  • , Sanna Vuoristo
  • , Tuula Salo
  • , Juha Kere
  • , Satu Wedenoja
  • , Päivi Saavalainen
  • *Corresponding author for this work
  • University of Helsinki
  • Karolinska Institutet
  • Folkhälsan Research Center
  • Helsinki University Hospital

Research output: Contribution to journalArticleScientificpeer-review

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Abstract

Oxygen tension varies during placental and fetal development. Although hypoxia drives early trophoblast invasion, low placental oxygen levels during pregnancy show association with pregnancy complications including fetal growth restriction and preeclampsia. JEG-3 cells are often used as a trophoblast model. We studied transcriptional changes of JEG-3 cells on a uterine leiomyoma derived matrix Myogel. This might be the closest condition to the real uterine environment that we can get for an in vitro model. We observed that culturing JEG-3 cells on the leiomyoma matrix leads to strong stimulation of ribosomal pathways, energy metabolism, and ATP production. Furthermore, Myogel improved JEG-3 cell adherence in comparison to tissue culture treated plastic. We also included PDMS microchip hypoxia creation, and observed changes in oxidative phosphorylation, oxygen related genes and several hypoxia genes. Our study highlights the effects of Myogel matrix on growing JEG-3 cells, especially on mitochondria, energy metabolism, and protein synthesis.

Original languageEnglish
Article number100056
Number of pages8
JournalBiomaterials and Biosystems
Volume7
Early online date22 Jun 2022
DOIs
Publication statusPublished - Aug 2022
MoE publication typeA1 Journal article-refereed

Keywords

  • Biomaterials
  • Hypoxia
  • JEG-3
  • Microenvironment
  • Microfluidic
  • Myogel
  • Oxygen scavenger
  • PDMS
  • Placenta
  • Pre-eclampsia

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