ResearchOrigins, actions and dynamic expression patterns of the neuropeptide VGF in rat peripheral and central sensory neurones following peripheral nerve injury1 UCL Department of Neuroscience, Physiology and Pharmacology, University College London, Gower Street, London, WC1E 6BT, UK 2 Neural Plasticity Research Group, Department of Anesthesia & Critical Care, Mass General Hospital & Harvard Medical School, 149 13th Street, Charlestown, MA 02129, USA 3 Fishberg Department of Neuroscience, Mount Sinai School of Medicine, New York, NY 10029, USA 4 Pfizer Global Research & Development, Pain Therapeutics, Ramsgate Road, Sandwich, Kent, CT13 9NJ, UK
Molecular Pain 2008, 4:62doi:10.1186/1744-8069-4-62
Additional filesAdditional file 1: Origins of terminal staining of VGF in the lumbar spinal cord. A. Immunohistochemistry of VGF (left) and CGRP (right) in the L4 spinal cord following unilateral L3–5 dorsal rhizotomy 5 days earlier. Ipsilateral CGRP depletion indicates total loss of primary afferent input. VGF staining in the region is decreased but not totally depleted (arrow). B. VGF (left) and 5 HT (right) immunostaining in L4 spinal cord following unilateral lesion of the dorsolateral funiculus at upper thoracic level 5 days earlier. Ipsilateral 5-HT depletion indicates loss of descending brainstem terminals, while VGF is only partially diminished (arrow). C Retrograde labeling of projection neurones in the rostroventral medulla, using bilateral True blue (2%) injection into the L4/5 spinal cord under anaesthetic, 5 days earlier (red), demonstrates expression of VGF in brainstem descending projection neurones. True blue:red. VGF:green. Double labeled: orange. Format: PPT Size: 4.7MB Download file This file can be viewed with: Microsoft PowerPoint Viewer Additional file 2: Origins of intrinisic staining of VGF in the lumbar spinal cord. A Immunohistochemistry for VGF and NeuN highlighting the ipsilateral increase in VGF in intrinsic dorsal horn neurones (Arrow). B High-power confocal immunohistochemistry of VGF and markers for microglia (Iba-1), neurones (NeuN) and astrocytes (GFAP) demonstrates that intrinsic VGF protein expression is co-localised specifically with the neuronal marker NeuN but not with either of the glial markers (arrows). Format: PPT Size: 2.8MB Download file This file can be viewed with: Microsoft PowerPoint Viewer |





on Google Scholar









author email
corresponding author email