Department of Developmental Neurobiology, St. Jude Children's Research Hospital, 262 Danny Thomas Place, Memphis, TN 38105, USA.
Science. 2010 Dec 24;330(6012):1834-8. doi: 10.1126/science.1198480. Epub 2010 Nov 25.
The brain's circuitry is established by directed migration and synaptogenesis of neurons during development. Although neurons mature and migrate in specific patterns, little is known about how neurons exit their germinal zone niche. We found that cerebellar granule neuron germinal zone exit is regulated by proteasomal degradation of Pard3A by the Seven in Absentia homolog (Siah) E3 ubiquitin ligase. Pard3A gain of function and Siah loss of function induce precocious radial migration. Time-lapse imaging using a probe to measure neuronal cell contact reveals that Pard3A promotes adhesive interactions needed for germinal zone exit by recruiting the epithelial tight junction adhesion molecule C to the neuronal cell surface. Our findings define a Siah-Pard3A signaling pathway that controls adhesion-dependent exit of neuronal progenitors or immature neurons from a germinal zone niche.
大脑的电路是通过神经元在发育过程中的定向迁移和突触发生建立的。虽然神经元以特定的模式成熟和迁移,但对于神经元如何离开其生发区龛位知之甚少。我们发现,小脑颗粒神经元生发区的退出受蛋白酶体降解 Pard3A 的调节,而 Pard3A 由 Seven in Absentia 同源物(Siah)E3 泛素连接酶降解。Pard3A 功能获得和 Siah 功能丧失会诱导过早的放射状迁移。使用探针测量神经元细胞接触的延时成像显示,Pard3A 通过将上皮紧密连接黏附分子 C 招募到神经元细胞表面,促进生发区退出所需的黏附相互作用。我们的研究结果定义了一个 Siah-Pard3A 信号通路,该通路控制着神经元祖细胞或未成熟神经元从生发区龛位依赖黏附的退出。