Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA.
Neuron. 2011 Sep 22;71(6):995-1013. doi: 10.1016/j.neuron.2011.07.026. Epub 2011 Sep 21.
A key obstacle to understanding neural circuits in the cerebral cortex is that of unraveling the diversity of GABAergic interneurons. This diversity poses general questions for neural circuit analysis: how are these interneuron cell types generated and assembled into stereotyped local circuits and how do they differentially contribute to circuit operations that underlie cortical functions ranging from perception to cognition? Using genetic engineering in mice, we have generated and characterized approximately 20 Cre and inducible CreER knockin driver lines that reliably target major classes and lineages of GABAergic neurons. More select populations are captured by intersection of Cre and Flp drivers. Genetic targeting allows reliable identification, monitoring, and manipulation of cortical GABAergic neurons, thereby enabling a systematic and comprehensive analysis from cell fate specification, migration, and connectivity, to their functions in network dynamics and behavior. As such, this approach will accelerate the study of GABAergic circuits throughout the mammalian brain.
理解大脑皮层神经回路的一个关键障碍是解开 GABA 能中间神经元的多样性。这种多样性给神经回路分析带来了一般性问题:这些中间神经元类型是如何产生并组装成定型的局部回路的,以及它们如何在从感知到认知等不同的皮层功能的回路操作中发挥作用?我们利用小鼠的基因工程,生成并鉴定了大约 20 条 Cre 和诱导型 CreER 敲入驱动线,这些驱动线可靠地靶向 GABA 能神经元的主要类别和谱系。通过 Cre 和 Flp 驱动的交叉,可以捕获更具选择性的群体。遗传靶向允许对皮质 GABA 能神经元进行可靠的识别、监测和操作,从而能够从细胞命运特化、迁移和连接,到它们在网络动态和行为中的功能进行系统和全面的分析。因此,这种方法将加速整个哺乳动物大脑中 GABA 能回路的研究。