Anderson S A, Marín O, Horn C, Jennings K, Rubenstein J L
Nina Ireland Laboratory of Developmental Neuroscience, Department of Psychiatry, University of California, San Francisco, CA 94143-0984, USA.
Development. 2001 Feb;128(3):353-63. doi: 10.1242/dev.128.3.353.
Recent evidence suggests that projection neurons and interneurons of the cerebral cortex are generally derived from distinct proliferative zones. Cortical projection neurons originate from the cortical ventricular zone (VZ), and then migrate radially into the cortical mantle, whereas most cortical interneurons originate from the basal telencephalon and migrate tangentially into the developing cortex. Previous studies using methods that label both proliferative and postmitotic cells have found that cortical interneurons migrate from two major subdivisions of the developing basal telencephalon: the medial and lateral ganglionic eminences (MGE and LGE). Since these studies labeled cells by methods that do not distinguish between the proliferating cells and those that may have originated elsewhere, we have studied the contribution of the MGE and LGE to cortical interneurons using fate mapping and genetic methods. Transplantation of BrdU-labeled MGE or LGE neuroepithelium into the basal telencephalon of unlabeled telencephalic slices enabled us to follow the fate of neurons derived from each of these primordia. We have determined that early in neurogenesis GABA-expressing cells from the MGE tangentially migrate into the cerebral cortex, primarily via the intermediate zone, whereas cells from the LGE do not. Later in neurogenesis, LGE-derived cells also migrate into the cortex, although this migration occurs primarily through the subventricular zone. Some of these LGE-derived cells invade the cortical plate and express GABA, while others remain within the cortical proliferative zone and appear to become mitotically active late in gestation. In addition, by comparing the phenotypes of mouse mutants with differential effects on MGE and LGE migration, we provide evidence that the MGE and LGE may give rise to different subtypes of cortical interneurons.
最近的证据表明,大脑皮层的投射神经元和中间神经元通常源自不同的增殖区。皮层投射神经元起源于皮层脑室区(VZ),然后径向迁移至皮层套层,而大多数皮层中间神经元起源于基底前脑,并切向迁移至发育中的皮层。以往使用标记增殖细胞和有丝分裂后细胞的方法进行的研究发现,皮层中间神经元从发育中的基底前脑的两个主要亚区迁移而来:内侧和外侧神经节隆起(MGE和LGE)。由于这些研究通过无法区分增殖细胞和可能起源于其他地方的细胞的方法标记细胞,我们使用命运图谱和遗传学方法研究了MGE和LGE对皮层中间神经元的贡献。将BrdU标记的MGE或LGE神经上皮移植到未标记的端脑切片的基底前脑,使我们能够追踪源自这些原基中每一个的神经元的命运。我们已经确定,在神经发生早期,来自MGE的表达GABA的细胞主要通过中间区切向迁移到大脑皮层,而来自LGE的细胞则不会。在神经发生后期,源自LGE的细胞也会迁移到皮层,尽管这种迁移主要通过脑室下区发生。这些源自LGE的细胞中的一些侵入皮层板并表达GABA,而另一些则保留在皮层增殖区,并在妊娠后期似乎变得有丝分裂活跃。此外,通过比较对MGE和LGE迁移有不同影响的小鼠突变体的表型,我们提供证据表明MGE和LGE可能产生不同亚型的皮层中间神经元。