Bloom David C, Watson Zachary L, Neumann Donna M
Department of Molecular Genetics and Microbiology, University of Florida College of Medicine, Gainesville, FL, USA.
Department of Obstetrics and Gynecology, University of Colorado School of Medicine, Aurora, CO, USA.
Methods Mol Biol. 2019;1950:237-247. doi: 10.1007/978-1-4939-9139-6_13.
Adeno-associated Virus (AAV) vectors are useful vehicles for delivering transgenes to a number of different tissues and organs in vivo. To date, most of these applications deliver the vectors to their target by either infusion into the bloodstream or direct injection into the target tissue. Recently there has been progress in delivering AAV vectors to neurons of the peripheral nervous system (PNS) following application of vectors to the peripheral epithelium, such as the skin or eye. This delivery only requires treatment of the epithelium to access the underlying nerve termini, and following treatment the vectors are transported retrogradely to the cell bodies of these neurons in the ganglia, such as dorsal root ganglia (DRG) or trigeminal ganglia (TG). Here we describe the methodology for highly efficient transduction of mouse DRG and rabbit TG following application of AAV vectors to the foot, or to the cornea, respectively.
腺相关病毒(AAV)载体是将转基因传递到体内多种不同组织和器官的有用工具。迄今为止,大多数这些应用通过注入血液或直接注射到靶组织将载体递送至其靶标。最近,在将AAV载体应用于外周上皮(如皮肤或眼睛)后,在将其递送至外周神经系统(PNS)的神经元方面取得了进展。这种递送仅需要处理上皮以进入下面的神经末梢,并且在处理后,载体逆行运输到神经节中这些神经元的细胞体,如背根神经节(DRG)或三叉神经节(TG)。在这里,我们分别描述了在将AAV载体应用于足部或角膜后高效转导小鼠DRG和兔TG的方法。