| Literature DB >> 26611592 |
Hongwei Yu1, Gregory Fischer2, Quinn H Hogan2.
Abstract
Transferring genetic molecules into the peripheral sensory nervous system to manipulate nociceptive pathophysiology is a powerful approach for experimental modulation of sensory signaling and potentially for translation into therapy for chronic pain. This can be efficiently achieved by the use of recombinant adeno-associated virus (rAAV) in conjunction with nociceptor-specific regulatory transgene cassettes. Among different routes of delivery, direct injection into the dorsal root ganglia (DRGs) offers the most efficient AAV-mediated gene transfer selectively into the peripheral sensory nervous system. Here, we briefly discuss the advantages and applications of intraganglionic microinjection, and then provide a detailed approach for DRG injection, including a list of the necessary materials and description of a method for performing DRG microinjection experiments. We also discuss our experience with several adeno-associated virus (AAV) options for in vivo transgene expression in DRG neurons.Entities:
Keywords: Adeno-associated virus; Chronic pain; Dorsal root ganglion; Gene therapy; Microinjection
Mesh:
Year: 2016 PMID: 26611592 PMCID: PMC5459312 DOI: 10.1007/978-1-4939-3271-9_18
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745