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Conditioning lesions enhance growth state only in sensory neurons lacking calcitonin gene-related peptide and isolectin B4-binding.
- Source :
-
Neuroscience [Neuroscience] 2010 Mar 10; Vol. 166 (1), pp. 107-21. Date of Electronic Publication: 2009 Dec 16. - Publication Year :
- 2010
-
Abstract
- A conditioning lesion improves regeneration of central and peripheral axons of dorsal root ganglion (DRG) neurons after a subsequent injury by enhancing intrinsic growth capacity. This enhanced growth state is also observed in cultured DRG neurons, which support a more sparsely and rapidly elongating mode of growth after a prior conditioning lesion in vivo. Here we examined differences in the capacity or requirements of specific types of sensory neurons for regenerative growth, which has important consequences for development of strategies to improve recovery after injury. We showed that after partial or complete injury of the sciatic nerve in mice, an elongating mode of growth in vitro was activated only in DRG neurons that did not express calcitonin gene-related peptide (CGRP) or bind Bandeiraea simplicifolia I-isolectin B4 (IB4). We also directly examined the response of conditioned sensory neurons to nerve growth factor (NGF), which does not enhance growth in injured peripheral nerves in vivo. We showed that after partial injury, NGF stimulated a highly branched and linearly restricted rather than elongating mode of growth. After complete injury, the function of NGF was impaired, which immunohistochemical studies of DRG indicated was at least partly due to downregulation of the NGF receptor, tropomyosin-related kinase A (TrkA). These results suggest that, regardless of the type of conditioning lesion, each type of DRG neuron has a distinct intrinsic capacity or requirement for the activation of rapidly elongating growth, which does not appear to be influenced by NGF.<br /> (Copyright 2010 IBRO. Published by Elsevier Ltd. All rights reserved.)
- Subjects :
- Animals
Calcitonin Gene-Related Peptide genetics
Cells, Cultured
Denervation
Ganglia, Spinal cytology
Ganglia, Spinal drug effects
Ganglia, Spinal injuries
Growth Cones drug effects
Growth Cones metabolism
Growth Cones ultrastructure
Immunohistochemistry
Male
Mice
Mice, Inbred C57BL
Nerve Growth Factor metabolism
Nerve Growth Factor pharmacology
Nerve Regeneration drug effects
Peripheral Nerve Injuries
Peripheral Nerves cytology
Peripheral Nerves drug effects
Plant Lectins metabolism
Receptor, trkA drug effects
Receptor, trkA metabolism
Recovery of Function physiology
Sciatic Neuropathy genetics
Sciatic Neuropathy physiopathology
Sensory Receptor Cells cytology
Sensory Receptor Cells drug effects
Signal Transduction drug effects
Signal Transduction physiology
Staining and Labeling
Calcitonin Gene-Related Peptide metabolism
Ganglia, Spinal metabolism
Nerve Regeneration physiology
Peripheral Nerves metabolism
Sciatic Neuropathy metabolism
Sensory Receptor Cells metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1873-7544
- Volume :
- 166
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Neuroscience
- Publication Type :
- Academic Journal
- Accession number :
- 20006678
- Full Text :
- https://doi.org/10.1016/j.neuroscience.2009.12.019