Department of Pediatrics, Nanjing Maternal and Child Health Hospital of Nanjing Medical University, Nanjing 210004, People's Republic of China.
Cell Biochem Biophys. 2011 Jul;60(3):259-66. doi: 10.1007/s12013-010-9148-2.
Fatty acid binding protein 3 (FABP3) is a member of a family of binding proteins. The protein is mainly expressed in cardiac and skeletal muscle cells, and it has been linked to fatty acid metabolism, trafficking, and signaling. Using suppression subtractive hybridization, we previously found that FABP3 is highly regulated in ventricular septal defect (VSD) patients and may play a significant role in the development of human VSD. We therefore aimed to identify the biological characteristics of the FABP3 gene in embryonic myocardial cells. On the basis of RT-PCR and western blotting analyses, we demonstrated that the expression levels of FABP3 mRNA and protein were up-regulated initially and then gradually decreased with P19 cell differentiation. MTT assays and cell cycle analysis showed that FABP3 inhibits P19 cell proliferation, and data from annexin V-FITC assays revealed that FABP3 can promote apoptosis of P19 cells. Further data from quantitative real-time RT-PCR revealed lower expression levels of cardiac muscle-specific molecular markers (cTnT, alpha-MHC, GATA4, and MEF2c) in FABP3-overexpressing cell lines than in the control cells during differentiation. Our results demonstrate that FABP3 may be involved in the differentiation of cardiac myocytes.
脂肪酸结合蛋白 3(FABP3)是结合蛋白家族的一员。该蛋白主要在心肌和骨骼肌细胞中表达,与脂肪酸代谢、运输和信号转导有关。我们之前使用抑制性消减杂交发现,FABP3 在室间隔缺损(VSD)患者中高度调控,可能在人类 VSD 的发生发展中起重要作用。因此,我们旨在鉴定 FABP3 基因在胚胎心肌细胞中的生物学特性。基于 RT-PCR 和 Western blot 分析,我们证明 FABP3 mRNA 和蛋白的表达水平最初上调,然后随着 P19 细胞分化逐渐下降。MTT 分析和细胞周期分析表明 FABP3 抑制 P19 细胞增殖,Annexin V-FITC 分析显示 FABP3 可促进 P19 细胞凋亡。定量实时 RT-PCR 的进一步数据显示,在分化过程中,过表达 FABP3 的细胞系中心肌特异性分子标志物(cTnT、alpha-MHC、GATA4 和 MEF2c)的表达水平较低。我们的结果表明,FABP3 可能参与心肌细胞的分化。