Fuller Patrick M, Yamanaka Akihiro, Lazarus Michael
Department of Neurology; Beth Israel Deaconess Medical Center; Division of Sleep Medicine; Harvard Medical School ; Boston, MA USA.
Department of Neuroscience II; Research Institute of Environmental Medicine; Nagoya University ; Nagoya, Aichi, Japan.
Temperature (Austin). 2015 Oct 12;2(3):406-17. doi: 10.1080/23328940.2015.1075095. eCollection 2015 Jul-Sep.
The advent of genetically engineered systems, including transgenic animals and recombinant viral vectors, has facilitated a more detailed understanding of the molecular and cellular substrates regulating brain function. In this review we highlight some of the most recent molecular biology and genetic technologies in the experimental "systems neurosciences," many of which are rapidly becoming a methodological standard, and focus in particular on those tools and techniques that permit the reversible and cell-type specific manipulation of neurons in behaving animals. These newer techniques encompass a wide range of approaches including conditional deletion of genes based on Cre/loxP technology, gene silencing using RNA interference, cell-type specific mapping or ablation and reversible manipulation (silencing and activation) of neurons in vivo. Combining these approaches with viral vector delivery systems, in particular adeno-associated viruses (AAV), has extended, in some instances greatly, the utility of these tools. For example, the spatially- and/or temporally-restricted transduction of specific neuronal cell populations is now routinely achieved using the combination of Cre-driver mice and stereotaxic-based delivery of AAV expressing Cre-dependent cassettes. We predict that the experimental application of these tools, including creative combinatorial approaches and the development of even newer reagents, will prove necessary for a complete understanding of the neuronal circuits subserving most neurobiological functions, including the regulation of sleep and wake.
基因工程系统的出现,包括转基因动物和重组病毒载体,有助于更详细地了解调节脑功能的分子和细胞底物。在本综述中,我们重点介绍实验性“系统神经科学”中一些最新的分子生物学和遗传技术,其中许多技术正迅速成为一种方法学标准,并特别关注那些能够在行为动物中对神经元进行可逆和细胞类型特异性操纵的工具和技术。这些更新的技术包括广泛的方法,如基于Cre/loxP技术的基因条件性缺失、使用RNA干扰的基因沉默、细胞类型特异性映射或消融以及体内神经元的可逆操纵(沉默和激活)。将这些方法与病毒载体递送系统,特别是腺相关病毒(AAV)相结合,在某些情况下极大地扩展了这些工具的效用。例如,现在通常使用Cre驱动小鼠和基于立体定位递送表达Cre依赖性盒式结构的AAV的组合,实现特定神经元细胞群体的空间和/或时间限制转导。我们预测,这些工具的实验应用,包括创造性的组合方法和更新试剂的开发,对于全面理解维持大多数神经生物学功能(包括睡眠和觉醒调节)的神经元回路将被证明是必要的。