Adams Niels C, Tomoda Toshifumi, Cooper Margaret, Dietz Gunnar, Hatten Mary E
Laboratory of Developmental Neurobiology, The Rockefeller University, 1230 York Avenue, New York, NY 10021-6399, USA.
Development. 2002 Feb;129(4):965-72. doi: 10.1242/dev.129.4.965.
The cortical regions of the brain are laminated as a result of directed migration of precursor cells along glia during development. Previously, we have used an assay system to identify astrotactin as a neuronal ligand for migration on glial fibers. To examine the function of astrotactin in vivo, we generated a null mutation by targeted gene disruption. The cerebella of astrotactin null mice are approximately 10% smaller than wild type. In vitro and in vivo cerebellar granule cell assays show a decrease in neuron-glial binding, a reduction in migration rates and abnormal development of Purkinje cells. Consequences of this are poorer balance and coordination. Thus, astrotactin functions in migration along glial processes in vivo, a process required for generating laminar structures and for the development of synaptic partner systems.
大脑的皮质区域在发育过程中由于前体细胞沿神经胶质细胞的定向迁移而形成分层结构。此前,我们利用一种检测系统鉴定出astrotactin是神经元在神经胶质纤维上迁移的配体。为了研究astrotactin在体内的功能,我们通过靶向基因敲除产生了一个无效突变。astrotactin基因敲除小鼠的小脑比野生型小鼠的小脑小约10%。体外和体内小脑颗粒细胞检测显示,神经元与神经胶质细胞的结合减少、迁移速率降低以及浦肯野细胞发育异常。由此产生的后果是平衡和协调能力较差。因此,astrotactin在体内沿神经胶质细胞突起的迁移中发挥作用,这是生成分层结构和突触伙伴系统发育所必需的过程。