Dynamic shifts in trophoblast nucleos(t)ide metabolism, transport, and adenosine signaling during gestation and preterm birth
Jazyk angličtina Země Velká Británie, Anglie Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
SVV2024/260 663
Ministerstvo Školství, Mládeže a Tělovýchovy
ID CZ.02.01.01/00/22_008/0004607
Ministerstvo Školství, Mládeže a Tělovýchovy
22-17643S
Grantová Agentura České Republiky
PubMed
40825832
PubMed Central
PMC12361576
DOI
10.1038/s41598-025-16183-2
PII: 10.1038/s41598-025-16183-2
Knihovny.cz E-zdroje
- Klíčová slova
- Adenosine receptors, Cytotrophoblast and syncytiotrophoblast, Nucleoside transporters, Nucleotide and nucleoside metabolism in placenta, Placental gene expression, Preterm birth,
- MeSH
- adenosin * metabolismus MeSH
- krysa rodu Rattus MeSH
- lidé MeSH
- placenta metabolismus MeSH
- předčasný porod * metabolismus genetika MeSH
- signální transdukce MeSH
- těhotenství MeSH
- trofoblasty * metabolismus MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- lidé MeSH
- těhotenství MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- adenosin * MeSH
Nucleos(t)ides are essential for DNA/RNA synthesis, energy metabolism, and signaling, yet their roles in placental development remain poorly understood. The placenta undergoes dynamic metabolic adaptations throughout gestation to support fetal growth. This study investigates gene expression shifts in nucleos(t)ide metabolism, transport, and adenosine signaling during placental development and in the pathological condition of spontaneous preterm birth (PTB). We analyzed gene expression in first-trimester (n = 10) and term (n = 10), and PTB (n = 10) human placentas, and in cytotrophoblast and syncytiotrophoblast stage in primary human trophoblasts (n = 3) and BeWo (n = 5) cells. For developmental context, rat placentas were examined at gestation days (GD) GD12, GD15, and GD20 (n = 5 per group) that correspond to early second trimester in the human placenta. We found that genes involved in nucleos(t)ide metabolism and adenosine signaling were dominantly upregulated from early gestation to term in the human placenta. PTB placentas revealed further elevation compared to the term placenta. Differentiation from cytotrophoblast to syncytiotrophoblast was accompanied by only minor changes. Pearson's correlation analysis revealed strong gene-metabolite and gene-gene associations, highlighting an integrated metabolic network regulating placental function. Gene expression also differed among the tested GDs in the rat placenta. These findings demonstrate dynamic changes of nucleos(t)ide metabolism during healthy placental development and enhanced expression in PTB placentas, suggesting increasing needs for nucleos(t)ides during placental growth and metabolic shifts in the PTB placenta. Our data also indicate that nucleos(t)ide metabolism is preserved in both proliferative and differentiated states.
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