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Origins, actions and dynamic expression patterns of the neuropeptide VGF in rat peripheral and central sensory neurones following peripheral nerve injury

Andrew Moss1,4 email, Rachel Ingram1 email, Stephanie Koch1 email, Andria Theodorou1 email, Lucie Low1 email, Mark Baccei1 email, Gareth J Hathway1 email, Michael Costigan2 email, Stephen R Salton3 email and Maria Fitzgerald1 email

UCL Department of Neuroscience, Physiology and Pharmacology, University College London, Gower Street, London, WC1E 6BT, UK

Neural Plasticity Research Group, Department of Anesthesia & Critical Care, Mass General Hospital & Harvard Medical School, 149 13th Street, Charlestown, MA 02129, USA

Fishberg Department of Neuroscience, Mount Sinai School of Medicine, New York, NY 10029, USA

Pfizer Global Research & Development, Pain Therapeutics, Ramsgate Road, Sandwich, Kent, CT13 9NJ, UK

author email corresponding author email

Molecular Pain 2008, 4:62doi:10.1186/1744-8069-4-62

Published: 10 December 2008

Additional files

Additional 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.

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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).

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