Developmental Neurobiology Unit, Instituto de Neurociencias de Alicante, CSIC - Universidad Miguel Hernandez, Av. Ramon y Cajal s/n, Sant Joan d'Alacant, 03550 Alicante, Spain.
J Neurosci Methods. 2010 Feb 15;186(2):186-95. doi: 10.1016/j.jneumeth.2009.11.016. Epub 2009 Nov 26.
Ferrets have been extensively used to unravel the neural mechanisms of coding and processing of visual information, and also to identify the developmental mechanisms underlying the emergence of such a complex and fine-tuned neural system. In recent years numerous tools have been generated that allow studying neural systems with unprecedented power. Unfortunately, because many of these tools are genetically encoded, they are having a limited impact on research involving "non-genetic" species, like ferret, cat and monkey. Here I show how in vivo electroporation can be performed in postnatal ferret kits to deliver genetic constructs to pyramidal neurons of the cerebral cortex. Electroporation of GFP- and DsRed-encoding plasmids results in labeling of cortical progenitors first, then migrating neurons, and finally differentiating neurons and their processes. This technique also allows for the genetic manipulation of cortical development in the ferret, as illustrated by electroporation of a dominant-negative form of Cdk5. In the mature brain of electroporated animals, expression of reporter genes reveals the detailed morphological traits of cortical pyramids, including their axonal and dendritic arborization, and dendritic spines. I also show that postnatal electroporation can be used for the transfection of a massive cortical territory, or it can be specifically directed to a subset of cortical areas, and even only to a few scattered pyramids along the cortical mantle. In vivo electroporation of postnatal ferrets is therefore an effective, rapid, simple and highly versatile method for delivering genetic constructs to this animal, optimal for both developmental studies and adult anatomical/functional studies.
雪貂被广泛用于揭示视觉信息编码和处理的神经机制,也用于鉴定出现如此复杂和精细的神经网络的发育机制。近年来,产生了许多工具,使我们能够以前所未有的能力研究神经系统。不幸的是,由于许多这些工具是基因编码的,它们对涉及“非遗传”物种(如雪貂、猫和猴子)的研究的影响有限。在这里,我展示了如何在出生后的雪貂幼崽中进行活体电穿孔,以将遗传构建体递送至大脑皮层的锥体神经元。GFP 和 DsRed 编码质粒的电穿孔导致皮质祖细胞首先被标记,然后是迁移神经元,最后是分化神经元及其突起。这项技术还允许对雪貂的皮质发育进行基因操作,如图示电穿孔 Cdk5 的显性负形式。在电穿孔动物的成熟大脑中,报告基因的表达揭示了皮质锥体的详细形态特征,包括其轴突和树突分支,以及树突棘。我还表明,出生后电穿孔可用于转染大量皮质区域,也可特异性地靶向皮质区域的子集,甚至仅靶向皮质盖的几个分散的锥体。因此,活体电穿孔是向这种动物传递遗传构建体的有效、快速、简单和高度通用的方法,最适合发育研究和成年解剖/功能研究。