Rice D S, Curran T
Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, USA.
Annu Rev Neurosci. 2001;24:1005-39. doi: 10.1146/annurev.neuro.24.1.1005.
The neurological mutant mouse reeler has played a critical role in the evolution of our understanding of normal brain development. From the earliest neuroanatomic studies of reeler, it was anticipated that the characterization of the gene responsible would elucidate important molecular and cellular principles governing cell positioning and the formation of synaptic circuits in the developing brain. Indeed, the identification of reelin has challenged many of our previous notions and has led to a new vision of the events involved in the migration of neurons. Several neuronal populations throughout the brain secrete Reelin, which binds to transmembrane receptors located on adjacent cells triggering a tyrosine kinase cascade. This allows neurons to complete migration and adopt their ultimate positions in laminar structures in the central nervous system. Recent studies have also suggested a role for the Reelin pathway in axonal branching, synaptogenesis, and pathology underlying neurodegeneration.
神经学突变小鼠“reeler”在我们对正常脑发育的理解演变过程中发挥了关键作用。从对“reeler”最早的神经解剖学研究开始,人们就预期确定相关基因的特征将阐明控制发育中大脑细胞定位和突触回路形成的重要分子和细胞原理。事实上,“reelin”的鉴定挑战了我们之前的许多观念,并引发了对神经元迁移相关事件的新认识。整个大脑中的几个神经元群体分泌“Reelin”,它与位于相邻细胞上的跨膜受体结合,触发酪氨酸激酶级联反应。这使得神经元能够完成迁移并在中枢神经系统的层状结构中占据其最终位置。最近的研究还表明“Reelin”信号通路在轴突分支、突触形成以及神经退行性变的病理过程中发挥作用。