Vomund Sandra, Sapir Tamar, Reiner Orly, Silva Maria A de Souza, Korth Carsten
Department of Neuropathology, Medical School Düsseldorf.
J Vis Exp. 2013 Sep 24(79):e50146. doi: 10.3791/50146.
In utero electroporation (IUE) is a technique which allows genetic modification of cells in the brain for investigating neuronal development. So far, the use of IUE for investigating behavior or neuropathology in the adult brain has been limited by insufficient methods for monitoring of IUE transfection success by non-invasive techniques in postnatal animals. For the present study, E16 rats were used for IUE. After intraventricular injection of the nucleic acids into the embryos, positioning of the tweezer electrodes was critical for targeting either the developing cortex or the hippocampus. Ventricular co-injection and electroporation of a luciferase gene allowed monitoring of the transfected cells postnatally after intraperitoneal luciferin injection in the anesthetized live P7 pup by in vivo bioluminescence, using an IVIS Spectrum device with 3D quantification software. Area definition by bioluminescence could clearly differentiate between cortical and hippocampal electroporations and detect a signal longitudinally over time up to 5 weeks after birth. This imaging technique allowed us to select pups with a sufficient number of transfected cells assumed necessary for triggering biological effects and, subsequently, to perform behavioral investigations at 3 month of age. As an example, this study demonstrates that IUE with the human full length DISC1 gene into the rat cortex led to amphetamine hypersensitivity. Co-transfected GFP could be detected in neurons by post mortem fluorescence microscopy in cryosections indicating gene expression present at ≥6 months after birth. We conclude that postnatal bioluminescence imaging allows evaluating the success of transient transfections with IUE in rats. Investigations on the influence of topical gene manipulations during neurodevelopment on the adult brain and its connectivity are greatly facilitated. For many scientific questions, this technique can supplement or even replace the use of transgenic rats and provide a novel technology for behavioral neuroscience.
子宫内电穿孔(IUE)是一种可对大脑中的细胞进行基因改造以研究神经元发育的技术。到目前为止,在出生后的动物中,由于缺乏通过非侵入性技术监测IUE转染成功率的有效方法,IUE在成人大脑行为或神经病理学研究中的应用受到限制。在本研究中,使用E16大鼠进行IUE。在将核酸脑室内注射到胚胎后,镊子电极的定位对于靶向发育中的皮层或海马至关重要。通过在麻醉的P7幼崽腹腔内注射荧光素后,利用配备3D定量软件的IVIS Spectrum设备进行体内生物发光,可对荧光素酶基因进行脑室共同注射和电穿孔,从而在出生后监测转染细胞。通过生物发光进行区域定义可以清楚地区分皮层和海马电穿孔,并在出生后长达5周的时间内纵向检测信号。这种成像技术使我们能够选择具有足够数量转染细胞的幼崽,这些细胞被认为是触发生物学效应所必需的,随后在3个月大时进行行为研究。例如,本研究表明,将人类全长DISC1基因通过IUE导入大鼠皮层会导致对苯丙胺过敏。死后在冰冻切片中通过荧光显微镜可在神经元中检测到共转染的绿色荧光蛋白(GFP),表明出生后≥6个月仍存在基因表达。我们得出结论,出生后生物发光成像可用于评估大鼠IUE瞬时转染的成功率。这极大地促进了对神经发育过程中局部基因操作对成人大脑及其连接性影响的研究。对于许多科学问题,该技术可以补充甚至取代转基因大鼠的使用,并为行为神经科学提供一种新技术。