Uteroplacental insufficiency alters hepatic expression, phosphorylation, and activity of the glucocorticoid receptor in fetal IUGR rats

• DOI: 10.1152/ajpregu.00211.2005
• Publication Date: 2005-07-07T20:35:40Z
• Authors: Mariana Baserga; Merica A. Hale; Robert A. McKnight; Xing Yu; Christopher W. Ca...; Robert H. Lane
• Keywords: 0301 basic medicine; Fetal Growth Retardation; Gene Expression Regulation, Developmental; Cyclin A; Placental Insufficiency; Chromatin; Rats; 3. Good health; Rats, Sprague-Dawley; 03 medical and health sciences; Receptors, Glucocorticoid; Liver; Pregnancy; Serine; Animals; Female; RNA, Messenger; Phosphorylation; Tumor Suppressor Protein p53; Corticosterone

Uteroplacental insufficiency (UPI) induces persistent changes in hepatic gene expression secondary to altered chromatin dynamics in the intrauterine growth- restricted (IUGR) rat liver. The glucocorticoid receptor (GR) is a transcription factor that when activated can induce changes in chromatin structure. To begin the process of identifying pathways by which IUGR affects chromatin structure, we hypothesized that UPI in the rat induces a significant increase in endogenous glucocorticoids (corticosterone) and increases GR expression and activation. To prove our hypothesis, we induced IUGR through bilateral uterine artery ligation of the pregnant rat. At day 1, UPI significantly increased corticosterone levels and was associated with increased total GR mRNA and protein levels in the liver, as well as increased hepatic phosphorylation of GR serine 211. Moreover, cyclin-dependent kinase 2 (CDK2) cyclinA/CDK2 protein levels, which selectively phosphorylate GR serine 211, were also significantly increased. To assess activity of the GR, we measured protein levels of the transcription factor p53 whose levels are downregulated, at least in part, by active GR. In this study, UPI decreased p53 protein and its downstream target Bax mRNA levels. We conclude that UPI in rats affects GR expression and activity in the liver. We speculate that these alterations early in life may contribute to the changes in chromatin structure and gene expression previously described in the IUGR liver.