Haenraets Karen, Albisetti Gioele W, Foster Edmund, Wildner Hendrik
Institute of Pharmacology and Toxicology, University of Zurich; Institute of Pharmaceutical Sciences, Swiss Federal Institute (ETH) Zurich.
Institute of Pharmacology and Toxicology, University of Zurich.
J Vis Exp. 2018 May 12(135):57382. doi: 10.3791/57382.
Selective manipulation of spinal neuronal subpopulations has mainly been achieved by two different methods: 1) Intersectional genetics, whereby double or triple transgenic mice are generated in order to achieve selective expression of a reporter or effector gene (e.g., from the Rosa26 locus) in the desired spinal population. 2) Intraspinal injection of Cre-dependent recombinant adeno-associated virus (rAAV); here Cre-dependent AAV vectors coding for the reporter or effector gene of choice are injected into the spinal cord of mice expressing Cre recombinase in the desired neuronal subpopulation. This protocol describes how to generate Cre-dependent rAAV vectors and how to transduce neurons in the dorsal horn of the lumbar spinal cord segments L3-L5 with rAAVs. As the lumbar spinal segments L3-L5 are innervated by those peripheral sensory neurons that transmit sensory information from the hindlimbs, spontaneous behavior and responses to sensory tests applied to the hindlimb ipsilateral to the injection side can be analyzed in order to interrogate the function of the manipulated neurons in sensory processing. We provide examples of how this technique can be used to analyze genetically defined subsets of spinal neurons. The main advantages of virus-mediated transgene expression in Cre transgenic mice compared to classical reporter mouse-induced transgene expression are the following: 1) Different Cre-dependent rAAVs encoding various reporter or effector proteins can be injected into a single Cre transgenic line, thus overcoming the need to create several multiple transgenic mouse lines. 2) Intraspinal injection limits manipulation of Cre-expressing cells to the injection site and to the time after injection. The main disadvantages are: 1) Reporter gene expression from rAAVs is more variable. 2) Surgery is required to transduce the spinal neurons of interest. Which of the two methods is more appropriate depends on the neuron population and research question to be addressed.
1)交叉遗传学方法,即通过培育双转基因或三转基因小鼠,以实现在所需脊髓神经元群体中选择性表达报告基因或效应基因(例如,来自Rosa26基因座)。2)脊髓内注射依赖Cre的重组腺相关病毒(rAAV);在此方法中,将编码所选报告基因或效应基因的依赖Cre的AAV载体注射到在所需神经元亚群中表达Cre重组酶的小鼠脊髓中。本方案描述了如何生成依赖Cre的rAAV载体,以及如何用rAAV转导腰髓L3-L5节段背角的神经元。由于腰髓L3-L5节段由那些从后肢传递感觉信息的外周感觉神经元支配,因此可以分析自发行为以及对注射侧后肢施加的感觉测试的反应,以探究被操控神经元在感觉处理中的功能。我们提供了如何使用该技术分析脊髓神经元的基因定义亚群的示例。与经典报告基因小鼠诱导的转基因表达相比,在Cre转基因小鼠中病毒介导的转基因表达的主要优点如下:1)可以将编码各种报告蛋白或效应蛋白的不同依赖Cre的rAAV注射到单个Cre转基因品系中,从而无需创建多个多转基因小鼠品系。2)脊髓内注射将对表达Cre的细胞的操控限制在注射部位和注射后的时间段内。主要缺点是:1)rAAV的报告基因表达变化更大。2)需要通过手术来转导感兴趣的脊髓神经元。两种方法中哪种更合适取决于要研究的神经元群体和研究问题。