Department of Genetics and Pathology, Uppsala University, Rudbeck Laboratory, Uppsala, Sweden.
Exp Cell Res. 2010 Oct 15;316(17):2779-89. doi: 10.1016/j.yexcr.2010.07.009. Epub 2010 Jul 17.
Platelet-derived growth factor (PDGF) is important in central nervous system (CNS) development, and aberrant expression of PDGF and its receptors has been linked to developmental defects and brain tumorigenesis. We previously found that neural stem and progenitor cells in culture produce PDGF and respond to it by autocrine and/or paracrine signaling. We therefore aimed to examine CNS development after PDGF overexpression in neural stem cells in vivo. Transgenic mice were generated with PDGF-B under control of a minimal nestin enhancer element, which is specific for embryonic expression and will not drive adult expression in mice. The resulting mouse showed increased apoptosis in the developing striatum, which suggests a disturbed regulation of progenitor cells. Later in neurodevelopment, in early postnatal life, mice displayed enlarged lateral ventricles. This enlargement remained into adulthood and it was more pronounced in male mice than in transgenic female mice. Nevertheless, there was an overall normal composition of cell types and numbers in the brain and the transgenic mice were viable and fertile. Adult transgenic males, however, showed behavioral aberrations and locomotor dysfunction. Thus, a tightly regulated expression of PDGF during embryogenesis is required for normal brain development and function in mice.
血小板衍生生长因子 (PDGF) 在中枢神经系统 (CNS) 发育中很重要,PDGF 及其受体的异常表达与发育缺陷和脑肿瘤发生有关。我们之前发现,培养中的神经干细胞和祖细胞产生 PDGF,并通过自分泌和/或旁分泌信号对其作出反应。因此,我们旨在研究体内神经干细胞中 PDGF 过表达后对 CNS 发育的影响。通过 PDGF-B 在最小 nestin 增强子元件的控制下生成转基因小鼠,该元件特异性用于胚胎表达,不会在小鼠中驱动成年表达。结果表明,发育中的纹状体中的细胞凋亡增加,这表明祖细胞的调节受到干扰。在神经发育的后期,即出生后早期,小鼠的侧脑室增大。这种增大持续到成年期,雄性小鼠比转基因雌性小鼠更为明显。然而,大脑中的细胞类型和数量总体上正常,转基因小鼠具有生存能力和繁殖能力。然而,成年雄性转基因小鼠表现出行为异常和运动功能障碍。因此,在胚胎发生过程中,PDGF 的严格调控表达对于小鼠的正常大脑发育和功能是必需的。