Hevner R F, Shi L, Justice N, Hsueh Y, Sheng M, Smiga S, Bulfone A, Goffinet A M, Campagnoni A T, Rubenstein J L
Nina Ireland Laboratory of, Developmental Neurobiology, Department of Psychiatry, University of California, San Francisco, San Francisco, CA 94143, USA.
Neuron. 2001 Feb;29(2):353-66. doi: 10.1016/s0896-6273(01)00211-2.
During corticogenesis, early-born neurons of the preplate and layer 6 are important for guiding subsequent neuronal migrations and axonal projections. Tbr1 is a putative transcription factor that is highly expressed in glutamatergic early-born cortical neurons. In Tbr1-deficient mice, these early-born neurons had molecular and functional defects. Cajal-Retzius cells expressed decreased levels of Reelin, resulting in a reeler-like cortical migration disorder. Impaired subplate differentiation was associated with ectopic projection of thalamocortical fibers into the basal telencephalon. Layer 6 defects contributed to errors in the thalamocortical, corticothalamic, and callosal projections. These results show that Tbr1 is a common genetic determinant for the differentiation of early-born glutamatergic neocortical neurons and provide insights into the functions of these neurons as regulators of cortical development.
在皮质发生过程中,前板和第6层的早期生成神经元对于引导后续神经元迁移和轴突投射至关重要。Tbr1是一种假定的转录因子,在谷氨酸能早期生成的皮质神经元中高度表达。在Tbr1基因缺陷小鼠中,这些早期生成的神经元存在分子和功能缺陷。Cajal-Retzius细胞中Reelin表达水平降低,导致类似reeler小鼠的皮质迁移障碍。板下区分化受损与丘脑皮质纤维异位投射至基底前脑有关。第6层缺陷导致丘脑皮质、皮质丘脑和胼胝体投射出现错误。这些结果表明,Tbr1是早期生成的谷氨酸能新皮质神经元分化的共同遗传决定因素,并为这些神经元作为皮质发育调节因子的功能提供了见解。