Thévenot Etienne, Côté Francine, Colin Philippe, He Yi, Leblois Hélène, Perricaudet Michel, Mallet Jacques, Vodjdani Guilan
Laboratoire de Génétique Moléculaire de la Neurotransmission et des Processus Neurodégénératifs, CNRS UMR 7091, Bâtiment CERVI, Hôpital de la Pitié-Salpêtrière, 83 boulevard de l'Hôpital, 75013 Paris, France.
Mol Cell Neurosci. 2003 Sep;24(1):139-47. doi: 10.1016/s1044-7431(03)00131-3.
Delivery of viral vectors encoding the Cre recombinase is showing promise to target gene modification in specific brain regions. Here we describe the targeting of the dorsal raphe nucleus (DRN), which contains the majority of the serotonin (5-HT) neurons projecting to the forebrain. First, we demonstrate successful transgene expression in the mouse DRN by stereotaxic delivery of the AdnlslacZ adenoviral vector. Second, we show that expression of the Cre recombinase can be achieved in the 5-HT neurons by optimized injection of the Adcre vector. Using reporter mice in which Cre activity induces beta-galactosidase (beta-gal) expression, we demonstrate efficient Cre-mediated recombination and persistence of beta-gal positive 5-HT neurons at least 1 month postinjection. Together, these results demonstrate that viral delivery provides a valuable method to target Cre recombination throughout the murine DRN and thus to study 5-HT neurotransmission by conditional gene modification.
递送编码Cre重组酶的病毒载体有望在特定脑区实现靶向基因修饰。在此,我们描述了对中缝背核(DRN)的靶向,该核包含投射到前脑的大多数5-羟色胺(5-HT)神经元。首先,我们通过立体定位递送AdnlslacZ腺病毒载体,证明了在小鼠DRN中成功实现转基因表达。其次,我们表明,通过优化注射Adcre载体,可在5-HT神经元中实现Cre重组酶的表达。利用Cre活性可诱导β-半乳糖苷酶(β-gal)表达的报告小鼠,我们证明了高效的Cre介导的重组以及注射后至少1个月β-gal阳性5-HT神经元的持续存在。总之,这些结果表明,病毒递送为在整个小鼠DRN中靶向Cre重组提供了一种有价值的方法,从而可通过条件性基因修饰来研究5-HT神经传递。