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fatty acid-binding protein month download article/chapter lentiviral-mediated rna interference kejiang cao & lingmei qian fabp3 gene silencing quantitative real-time pcr real-time quantitative pcr lentiviral-based vector system genome-wide array analysis inducing mitochondrial impairment gene regulatory networks human gene therapy silence gene expression embryonic carcinoma cells article cell biochemistry fabp3 inhibited proliferation full article pdf embryonic myocardial cells embryonic cancer cells congenital heart disease congenital heart malformations privacy choices/manage cookies gata-4 transcription factor p19 cell differentiation rna interference embryonic heart development early apoptotic cells fluorescein labelled annexin genetic regulation targeting mitochondria embryonic cardiac malformations related subjects ventricular septal defect differentially expressed genes pulmonary endothelial cells fabp3 inhibits proliferation article shen biophysical research communications fabp3 promotes apoptosis european economic area cck-8 proliferation assays concise promoter region suppression subtractive hybridization high-efficiency transformation flow cytometric detection induces mitochondrion impairment apoptotic/mytogenic pathways promoted apoptosis human heart development malformed human hearts

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      description:Fatty acid–binding protein 3 (FABP3) facilitates the movement of fatty acids in cardiac muscle. Previously, we reported that FABP3 is highly upregulated in the myocardium of ventricular septal defect patients and overexpression of FABP3 inhibited proliferation and promoted apoptosis in embryonic carcinoma cells (P19 cells). In this study, we aimed to investigate the effect of FABP3 gene silencing on P19 cell differentiation, proliferation and apoptosis. We used RNA interference and a lentiviral-based vector system to create a stable FABP3-silenced P19 cell line; knockdown of FABP3 was confirmed by quantitative real-time PCR. Expression analysis of specific differentiation marker genes using quantitative real-time PCR and observation of morphological changes using an inverted microscope revealed that knockdown of FABP3 did not significantly affect the differentiation of P19 cells into cardiomyocytes. CCK-8 proliferation assays and cell cycle analysis demonstrated that FABP3 gene silencing significantly inhibited P19 cell proliferation. Furthermore, Annexin V-FITC/propidium iodide staining and the caspase-3 activity assay revealed that FABP3 gene silencing significantly promoted serum starvation–induced apoptosis in P19 cells. In agreement with our previous research, these results demonstrate that FABP3 may play an important role during embryonic heart development, and that either overexpression or silencing of FABP3 will lead to an imbalance between proliferation and apoptosis, which may result in embryonic cardiac malformations.
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