In utero sFlt-1 exposure differentially affects gene expression patterns in fetal liverStojanovska, V., Holwerda, K. M., van der Graaf, A. M., Verkaik-Schakel, R. N., Boekschoten, M. V., Faas, M. M., Scherjon, S. A. & Plösch, T., Jun-2019, In : Journal of developmental origins of health and disease. 10, 3, p. 353-361 9 p.
Research output: Contribution to journal › Article › Academic › peer-review
The soluble fms-like tyrosine kinase factor 1 (sFlt-1) is a major contributor to antiangiogenesis during preeclampsia. However, little is known about the effects of sFlt-1 on fetal health. In this study we aim to evaluate the effects of the sFlt-1 concentration during pregnancy on fetal liver physiology. We used adenoviral gene delivery in Sprague-Dawley dams (seven females, 10 weeks old) during mid-gestation (gestational day 8) with adenovirus overexpressing sFlt-1, and age-matched controls (six females, 10 weeks old) with empty adenoviral virus in order to quantify the sFlt-1 concentrations in pregnant dams. Dams exposed to adenoviral sFlt-1 delivery were subdivided into a low (n=4) and high sFlt-1 (n=3) group based on host response to the virus. One-way analysis of variance showed that fetuses (five per dam) exposed to high sFlt-1 concentrations in utero show fetal growth restriction (1.84±0.043 g high sFlt-1 v. 2.32±0.036 g control; mean (M)±s.e.m.; P<0.001), without hypertension or proteinuria in the dams. In continuation, the microarray analysis of the fetal liver of the high sFlt-1 group showed significant enrichment of key genes for fatty acid metabolism and Ppara targets. In addition, using pyrosequencing, we found that the Ppara enrichment in the high sFlt-1 group is accompanied by decreased methylation of its promoter (1.89±0.097 mean % methylation in high sFlt-1 v. 2.26±0.095 mean % methylation in control, M±s.e.m., P<0.02). Our data show that high sFlt-1 concentrations during pregnancy have detrimental effects on the fatty acid metabolism genes and the Ppara targets in the fetal liver.
|Number of pages||9|
|Journal||Journal of developmental origins of health and disease|
|Early online date||10-Apr-2019|
|Publication status||Published - Jun-2019|
- animal, developmental stage, epigenetics, fetus, general, molecular/cellular, small animals, GROWTH-FACTOR RECEPTOR-1, BIRTH-WEIGHT, ANGIOGENIC FACTORS, PPAR-ALPHA, RESTRICTION, RETARDATION, METABOLISM, OBESITY, ALTERS, FLT-1