Harwell Corey C, Fuentealba Luis C, Gonzalez-Cerrillo Adrian, Parker Phillip R L, Gertz Caitlyn C, Mazzola Emanuele, Garcia Miguel Turrero, Alvarez-Buylla Arturo, Cepko Constance L, Kriegstein Arnold R
Department of Neurobiology, Harvard Medical School, Boston, MA 02115, USA.
Department of Neurological Surgery, University of California, San Francisco, San Francisco, CA 94143, USA; Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, San Francisco, CA 94143, USA.
Neuron. 2015 Sep 2;87(5):999-1007. doi: 10.1016/j.neuron.2015.07.030. Epub 2015 Aug 20.
The mammalian neocortex is composed of two major neuronal cell types with distinct origins: excitatory pyramidal neurons and inhibitory interneurons, generated in dorsal and ventral progenitor zones of the embryonic telencephalon, respectively. Thus, inhibitory neurons migrate relatively long distances to reach their destination in the developing forebrain. The role of lineage in the organization and circuitry of interneurons is still not well understood. Utilizing a combination of genetics, retroviral fate mapping, and lineage-specific retroviral barcode labeling, we find that clonally related interneurons can be widely dispersed while unrelated interneurons can be closely clustered. These data suggest that migratory mechanisms related to the clustering of interneurons occur largely independent of their clonal origin.
兴奋性锥体神经元和抑制性中间神经元,分别在胚胎端脑的背侧和腹侧祖细胞区产生。因此,抑制性神经元要迁移相对较长的距离才能到达发育中的前脑的目的地。谱系在中间神经元的组织和神经回路中的作用仍未得到充分理解。利用遗传学、逆转录病毒命运图谱和谱系特异性逆转录病毒条形码标记相结合的方法,我们发现克隆相关的中间神经元可以广泛分散,而不相关的中间神经元可以紧密聚集。这些数据表明,与中间神经元聚集相关的迁移机制在很大程度上独立于它们的克隆起源。