Chiaramello S, Dalmasso G, Bezin L, Marcel D, Jourdan F, Peretto P, Fasolo A, De Marchis S
Department of Animal and Human Biology, University of Turin, 10123 Turin, Italy.
Eur J Neurosci. 2007 Oct;26(7):1780-90. doi: 10.1111/j.1460-9568.2007.05818.x. Epub 2007 Sep 20.
Neuroblasts born in the subventricular zone (SVZ) migrate along the rostral migratory stream, reaching the olfactory bulb (OB) where they differentiate into local interneurons. Several extracellular factors have been suggested to control specific steps of this process. The brain-derived neurotrophic factor (BDNF) has been demonstrated to promote morphological differentiation and survival of OB interneurons. Here we show that BDNF and its receptor TrkB are expressed in vivo throughout the migratory pathway, implying that BDNF might also mediate migratory signals. By using in vitro models we demonstrate that BDNF promotes migration of SVZ neuroblasts, acting both as inducer and attractant through TrkB activation. We show that BDNF induces cAMP response element-binding protein (CREB) activation in migrating neuroblasts via phosphatidylinositol 3-kinase (PI3-K) and mitogen-activated protein kinase (MAP-K) signalling. Pharmacological blockade of these pathways on SVZ explants significantly reduces CREB activation and impairs neuronal migration. This study identifies a function of BDNF in the SVZ system, which involves multiple protein kinase pathways leading to neuroblast migration.
在脑室下区(SVZ)产生的神经母细胞沿着吻侧迁移流迁移,到达嗅球(OB),并在那里分化为局部中间神经元。已有多种细胞外因子被认为可控制这一过程的特定步骤。脑源性神经营养因子(BDNF)已被证明可促进嗅球中间神经元的形态分化和存活。我们在此表明,BDNF及其受体TrkB在体内整个迁移途径中均有表达,这意味着BDNF可能也介导迁移信号。通过使用体外模型,我们证明BDNF通过激活TrkB促进SVZ神经母细胞的迁移,兼具诱导剂和吸引剂的作用。我们发现BDNF通过磷脂酰肌醇3激酶(PI3-K)和丝裂原活化蛋白激酶(MAP-K)信号通路诱导迁移中的神经母细胞内的环磷酸腺苷反应元件结合蛋白(CREB)活化。对SVZ外植体进行这些信号通路的药理学阻断可显著降低CREB活化并损害神经元迁移。本研究确定了BDNF在SVZ系统中的一种功能,该功能涉及导致神经母细胞迁移的多条蛋白激酶信号通路。