Trupp M, Belluardo N, Funakoshi H, Ibáñez C F
Division of Molecular Neurobiology, Department of Neuroscience, Karolinska Institute, 171 77 Stockholm, Sweden.
J Neurosci. 1997 May 15;17(10):3554-67. doi: 10.1523/JNEUROSCI.17-10-03554.1997.
Glial cell line-derived neurotrophic factor (GDNF), the most potent trophic factor yet described for both dopaminergic neurons of the substantia nigra and spinal motorneurons, has recently been shown to signal through a multireceptor complex composed of a novel glycosylphosphatidylinositol-anchored GDNF receptor-alpha (GDNFR-alpha) and the receptor tyrosine kinase product of the c-ret proto-oncogene (RET). Despite its importance, the individual expression patterns and the relationships between domains of expression of the different components of this trophic system are not understood. We show here by in situ hybridization that GDNF mRNA is expressed in the normal adult rat brain in several targets of substantia nigra neurons, including striatum, nucleus accumbens, thalamic nuclei, olfactory tubercle, hippocampus, cerebellum, and cingulate cortex as well as in the internal granular cell layer of the olfactory bulb. Within the basal ganglia we observe a pronounced segregation of regions expressing GDNF from those expressing GDNF receptors, suggesting that within these structures GDNF is functioning in its anticipated role as a target-derived trophic factor. In addition, the expression of GDNF and both GDNF receptors within the cerebellum, hippocampus, and olfactory bulb may indicate a paracrine mode of action. Importantly, we also see expression of RET mRNA in cellular populations within the cerebellum and the glomerular layer of the olfactory bulb, as well as in the subthalamic nucleus, which lack GDNFR-alpha expression, indicating that RET functions either independently of GDNFR-alpha or with GDNFR-alpha presented in trans. Conversely, GDNFR-alpha is widely expressed in many regions in which RET expression is absent, suggesting that GDNFR-alpha may associate with additional signaling receptors. Finally, RET and GDNFR-alpha show distinct patterns of regulated expression in the brain after kainic acid stimulation and in the sciatic nerve after nerve transection. Taken together these findings indicate that GDNF, RET, and GDNFR-alpha utilize multiple mechanisms to comprise physiologically relevant trophic circuits for different neuronal populations.
胶质细胞系源性神经营养因子(GDNF)是迄今所描述的对黑质多巴胺能神经元和脊髓运动神经元最有效的营养因子,最近研究表明,它通过一种多受体复合物发挥信号传导作用,该复合物由一种新型糖基磷脂酰肌醇锚定的GDNF受体α(GDNFR-α)和原癌基因c-ret的受体酪氨酸激酶产物(RET)组成。尽管其很重要,但对该营养系统不同组分的个体表达模式以及表达域之间的关系仍不清楚。我们在此通过原位杂交表明,GDNF mRNA在正常成年大鼠脑中表达于黑质神经元的多个靶区,包括纹状体、伏隔核、丘脑核、嗅结节、海马、小脑、扣带回皮质以及嗅球的内颗粒细胞层。在基底神经节内,我们观察到表达GDNF的区域与表达GDNF受体的区域明显分离,这表明在这些结构中GDNF发挥着其作为靶源性营养因子的预期作用。此外,GDNF以及两种GDNF受体在小脑、海马和嗅球内的表达可能表明其旁分泌作用模式。重要的是,我们还在小脑和嗅球的肾小球层以及缺乏GDNFR-α表达的丘脑底核的细胞群体中观察到RET mRNA的表达,这表明RET要么独立于GDNFR-α发挥作用,要么与反式呈现的GDNFR-α一起发挥作用。相反,GDNFR-α在许多缺乏RET表达的区域广泛表达,这表明GDNFR-α可能与其他信号受体相关联。最后,在 kainic 酸刺激后,RET和GDNFR-α在脑中呈现出不同的表达调控模式,在坐骨神经横断后也是如此。综合这些发现表明,GDNF、RET和GDNFR-α利用多种机制为不同的神经元群体构成生理相关的营养回路。