Transforming Growth Factor α Evokes Aromatase Expression in Gastric Parietal Cells during Rat Postnatal Development.
Hiroto KobayashiAkira NaitoKyutaro KawagishiPublished in: International journal of molecular sciences (2024)
Estrogen, well known as a female hormone, is synthesized primarily by ovarian aromatase. However, extra-glandular tissues also express aromatase and produce estrogen. It is noteworthy that aromatase in gastric parietal cells begins expression around 20 days after birth and continues secreting considerable amounts of estrogen into the portal vein throughout life, supplying it to the liver. Estrogen, which is secreted from the stomach, is speculated to play a monitoring role in blood triglyceride, and its importance is expected to increase. Nevertheless, the regulatory mechanisms of the aromatase expression remain unclear. This study investigated the influence of transforming growth factor α (TGFα) on gastric aromatase expression during postnatal development. The administration of TGFα (50 μg/kg BW) to male Wistar rats in the weaning period resulted in enhanced aromatase expression and increased phosphorylated ERK1+2 in the gastric mucosa. By contrast, administration of AG1478 (5 mg/kg BW), a protein tyrosine kinase inhibitor with high selectivity for the epidermal growth factor receptor and acting as an antagonist of TGFα, led to the suppression of aromatase expression. In fact, TGFα expression in the gastric fundic gland isthmus began around 20 days after birth in normal rats as did that of aromatase, which indicates that TGFα might induce the expression of aromatase in the parietal cells concomitantly.
Keyphrases
- transforming growth factor
- poor prognosis
- epithelial mesenchymal transition
- binding protein
- epidermal growth factor receptor
- induced apoptosis
- preterm infants
- long non coding rna
- signaling pathway
- oxidative stress
- working memory
- computed tomography
- cell proliferation
- high resolution
- intensive care unit
- endoplasmic reticulum stress
- gestational age
- cell cycle arrest
- preterm birth
- acute respiratory distress syndrome
- mechanical ventilation
- quantum dots
- mass spectrometry