Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
4335212 | Journal of Neuroscience Methods | 2012 | 9 Pages |
BackgroundIn order to evaluate nerve regeneration in clinically relevant hindlimb surgical paradigms not feasible in fluorescent mice models, we developed a rat that expresses green fluorescent protein (GFP) in neural tissue.MethodsTransgenic Sprague-Dawley rat lines were created using pronuclear injection of a transgene expressing GFP under the control of the thy1 gene. Nerves were imaged under fluorescence microscopy and muscles were imaged with confocal microscopy to determine GFP expression following sciatic nerve crush, transection and direct suturing, and transection followed by repair with a nerve isograft from nonexpressing littermates.ResultsIn each surgical paradigm, fluorescence microscopy demonstrated the loss and reappearance of fluorescence with regeneration of axons following injury. Nerve regeneration was confirmed with imaging of Wallerian degeneration followed by reinnervation of extensor digitorum longus (EDL) muscle motor endplates using confocal microscopy.ConclusionThe generation of a novel transgenic rat model expressing GFP in neural tissue allows in vivo imaging of nerve regeneration and visualization of motor endplate reinnervation. This rat provides a new model for studying peripheral nerve injury and regeneration over surgically relevant distances.
► A rat was created that expresses GFP in nerves under thy1 promoter. ► Thy1-GFP rat serves as a new tool for evaluation of nerve injury and regeneration. ► Thy1- GFP rat allows for in vivo imaging of nerve regeneration with microscopy. ► Motor endplate reinnervation can be visualized in the thy1-GFP rat. ► Three hindlimb surgical paradigms demonstrate the potential for nerve research.