WWW.JNEUROSCI.ORG
-
The Journal of Neuroscience
 QUICK SEARCH:   [advanced]


     
-


HOME
  |  
SEARCH  |   ARCHIVE  |   SUBSCRIBE  |   CONTACT  |   HELP

This Article
Right arrow Full Text (PDF)
Right arrow Submit an eLetter
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (112)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Verge, V. M.
Right arrow Articles by Bisby, M. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Verge, V. M.
Right arrow Articles by Bisby, M. A.

 Previous Article  |  Next Article 

Journal of Neuroscience, Vol 10, 926-934, Copyright © 1990 by Society for Neuroscience


ARTICLE

Correlation between GAP43 and nerve growth factor receptors in rat sensory neurons

VM Verge, W Tetzlaff, PM Richardson and MA Bisby
Division of Neurosurgery, Montreal General Hospital, Canada.

In mature rat sensory neurons, expression of the gene for the growth- associated protein, GAP43, was studied by in situ hybridization with a cDNA probe. Among neurons in normal lumbar dorsal root ganglia, labeling for GAP43 mRNA was heterogeneous, approximately one-half of the neurons being densely labeled. To characterize the latter population, individual neurons were examined in adjacent sections processed either for GAP43 hybridization or NGF-receptor radioautography. Virtually all neurons with high-affinity NGF binding sites had high basal levels of GAP43 mRNA and most GAP43-positive neurons bore NGF receptors. Another NGF-responsive population, sympathetic neurons in the superior cervical ganglion, also had high basal concentrations of GAP43 mRNA. Further co-localization studies in dorsal root ganglia were performed with immunohistochemistry for somatostatin and enzyme histochemistry for acid phosphatase. The latter 2 groups of sensory neurons have been previously shown to lack high- affinity receptors and were here shown to have low basal concentrations of GAP43 mRNA. From this and earlier studies, it can be assumed that substance P-immunoreactive neurons and strongly positive CGRP neurons synthesize GAP43 at high basal rate. One week following peripheral nerve transection, almost all neurons had high concentrations of GAP43 mRNA without correlation with NGF binding. Intrathecal infusion of NGF after the sciatic nerve was cut did not strongly influence this post- traumatic elevation in GAP mRNA. In normal dorsal root ganglia, neurons that have high-affinity NGF binding sites and are therefore potentially responsive to NGF also have high basal rates of synthesis of GAP43.(ABSTRACT TRUNCATED AT 250 WORDS)


This article has been cited by other articles:


Home page
J. Neurosci.Home page
P. G. Leclere, E. Norman, F. Groutsi, R. Coffin, U. Mayer, J. Pizzey, and D. Tonge
Impaired Axonal Regeneration by Isolectin B4-Binding Dorsal Root Ganglion Neurons In Vitro
J. Neurosci., January 31, 2007; 27(5): 1190 - 1199.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
D. B. Arthur, K. Akassoglou, and P. A. Insel
P2Y2 receptor activates nerve growth factor/TrkA signaling to enhance neuronal differentiation
PNAS, December 27, 2005; 102(52): 19138 - 19143.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
M. S. Ramer, I. Duraisingam, J. V. Priestley, and S. B. McMahon
Two-Tiered Inhibition of Axon Regeneration at the Dorsal Root Entry Zone
J. Neurosci., April 15, 2001; 21(8): 2651 - 2660.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
P. G. Murphy, L. S. Borthwick, R. S. Johnston, G. Kuchel, and P. M. Richardson
Nature of the Retrograde Signal from Injured Nerves that Induces Interleukin-6 mRNA in Neurons
J. Neurosci., May 15, 1999; 19(10): 3791 - 3800.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
M. Costigan, R. J. Mannion, G. Kendall, S. E. Lewis, J. A. Campagna, R. E. Coggeshall, J. Meridith-Middleton, S. Tate, and C. J. Woolf
Heat Shock Protein 27: Developmental Regulation and Expression after Peripheral Nerve Injury
J. Neurosci., August 1, 1998; 18(15): 5891 - 5900.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
D. S. Smith and J. H. Pate Skene
A Transcription-Dependent Switch Controls Competence of Adult Neurons for Distinct Modes of Axon Growth
J. Neurosci., January 15, 1997; 17(2): 646 - 658.
[Abstract] [Full Text] [PDF]



-
-

Home  |   Search  |   Archive  |   Subscribe  |   Contact  |   Help

-
Copyright 2009 by Society for Neuroscience ONLINE ISSN: 1529-2401
-