Abstract

AbstractBackgroundThe objective of this study was to develop a cell culture system for fetal baboon hepatocytes and to test the hypotheses that (i) expression of the gluconeogenic enzyme phosphoenolpyruvate carboxykinase‐1 (PEPCK‐1) is upregulated in hepatocytes isolated from fetuses of nutrient‐restricted mothers (MNR) compared with ad libitum‐fed controls (CTR), and (ii) glucocorticoids stimulate PEPCK‐1 expression.MethodsHepatocytes from 0.9G CTR and MNR fetuses were isolated and cultured. PEPCK‐1 protein and mRNA levels in hepatocytes were determined by Western blot and quantitative PCR, respectively.ResultsFetuses of MNR mothers were intrauterine growth restricted (IUGR). Feasibility of culturing 0.9G fetal baboon hepatocytes was demonstrated. PEPCK‐1 protein levels were increased in hepatocytes isolated from IUGR fetuses, and PEPCK‐1 mRNA expression was stimulated by glucocorticoids in fetal hepatocytes.ConclusionsCultured fetal baboon hepatocytes that retain their in vivo phenotype provide powerful in vitro tools to investigate mechanisms that regulate normal and programmed hepatic function.

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