Magdaleno Susan, Keshvara Lakhu, Curran Tom
Department of Developmental Neurobiology, St. Jude Children's Research Hospital, 332 North Lauderdale, Memphis, TN 38105, USA.
Neuron. 2002 Feb 14;33(4):573-86. doi: 10.1016/s0896-6273(02)00582-2.
The gene mutated in reeler (reelin) encodes a protein secreted by neurons in the developing brain that controls laminar positioning of migrating cells in the CNS by an unknown mechanism. To investigate Reelin function, we used the nestin promoter to express Reelin ectopically in the ventricular zone and other brain regions in transgenic mice. In the presence of the endogenous protein, ectopic Reelin did not alter cell migration in the neocortex or the cerebellum. However, in the reeler background, ectopic Reelin induced tyrosine phosphorylation of Dab-1 in the ventricular zone and rescued some, but not all, of the neuroanatomic and behavioral abnormalities characteristic of reeler. These results indicate that Reelin does not function simply as a positional signal. Rather, it appears to participate in multiple events critical for neuronal migration and cell positioning.
在reeler小鼠中发生突变的基因(reelin)编码一种由发育中的大脑中的神经元分泌的蛋白质,该蛋白质通过未知机制控制中枢神经系统中迁移细胞的层状定位。为了研究Reelin的功能,我们使用巢蛋白启动子在转基因小鼠的脑室区和其他脑区异位表达Reelin。在内源蛋白存在的情况下,异位表达的Reelin并没有改变新皮层或小脑中的细胞迁移。然而,在reeler背景下,异位表达的Reelin在脑室区诱导Dab-1的酪氨酸磷酸化,并挽救了reeler小鼠部分而非全部的神经解剖学和行为异常特征。这些结果表明,Reelin不仅仅作为一种位置信号发挥作用。相反,它似乎参与了对神经元迁移和细胞定位至关重要的多个事件。