WWW.JNEUROSCI.ORG
-
The Journal of Neuroscience The New Axio Examiner
 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 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 Google Scholar
Google Scholar
Right arrow Articles by Perry, G. W.
Right arrow Articles by Grafstein, B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Perry, G. W.
Right arrow Articles by Grafstein, B.

 Previous Article  |  Next Article 

Journal of Neuroscience, Vol 7, 792-806, Copyright © 1987 by Society for Neuroscience


ARTICLE

Fast axonally transported proteins in regenerating goldfish optic axons

GW Perry, DW Burmeister and B Grafstein

Fast axonal transport of protein was examined in regenerating goldfish optic axons after a lesion of either the optic tract or optic nerve, which revealed changes in the original intact optic axon segments or in the newly regenerated axon segments, respectively. In animals killed either 6 or 24 hr after injection of 3H-proline into the eye, labeling of total fast-transported protein in the original axon segments was increased by 2 d after the lesion, reached a peak of nearly 20 X normal at 2 weeks, and then declined to a level somewhat above normal at 12 weeks. When the labeling of individual transported proteins was examined by 2-dimensional gel electrophoresis, it was found that no new labeled proteins appeared during regeneration, but all proteins examined showed an increase in labeling. Among the various proteins, there was great variation in the magnitude and time course of the labeling increase. The largest increase, to nearly 200 X normal with 6 hr labeling, was seen in a protein with a molecular weight of 45 kDa and a pl of about 4.5, resembling a protein that has previously been designated a "growth-associated protein" (GAP-43; Skene and Willard, 1981a). The proteins showing increased labeling included a small fraction of cytoskeletal proteins (alpha-tubulin, beta-tubulin, and actin) that was apparently transported at a much faster rate than is usually expected of these constituents. In the new axon segments, the total protein labeling was increased by 1 week after the lesion, remained elevated at a nearly constant level of about 7 X normal from about 2 to 5 weeks, and then declined to levels somewhat above normal by 12 weeks. The 45 kDa protein again showed the largest increase, and became the single most prominently labeled constituent in the new axons. On the basis of the time course of labeling in both original and new axon segments during regeneration, the fast-transported proteins were tentatively separated into 5 classes that may represent groups of proteins that are coregulated during regeneration. They may conceivably correspond to different functional or structural entities within the neuron.


This article has been cited by other articles:


Home page
J. Neurosci.Home page
B. V. Fausett and D. Goldman
A role for alpha1 tubulin-expressing Muller glia in regeneration of the injured zebrafish retina.
J. Neurosci., June 7, 2006; 26(23): 6303 - 6313.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
M.-C. Senut, A. Gulati-Leekha, and D. Goldman
An Element in the {alpha}1-Tubulin Promoter Is Necessary for Retinal Expression during Optic Nerve Regeneration But Not after Eye Injury in the Adult Zebrafish
J. Neurosci., September 1, 2004; 24(35): 7663 - 7673.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
B. Petrausch, R. Tabibiazar, T. Roser, Y. Jing, D. Goldman, C. A. O. Stuermer, N. Irwin, and L. I. Benowitz
A Purine-Sensitive Pathway Regulates Multiple Genes Involved in Axon Regeneration in Goldfish Retinal Ganglion Cells
J. Neurosci., November 1, 2000; 20(21): 8031 - 8041.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
L. R. Banner, P. H. Patterson, A. Allchorne, S. Poole, and C. J. Woolf
Leukemia Inhibitory Factor Is an Anti-Inflammatory and Analgesic Cytokine
J. Neurosci., July 15, 1998; 18(14): 5456 - 5462.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
T Schulte, K. Paschke, U Laessing, F Lottspeich, and C. Stuermer
Reggie-1 and reggie-2, two cell surface proteins expressed by retinal ganglion cells during axon regeneration
Development, January 1, 1997; 124(2): 577 - 587.
[Abstract] [PDF]


Home page
DevelopmentHome page
E Reinhard, E Nedivi, J Wegner, J. Skene, and M Westerfield
Neural selective activation and temporal regulation of a mammalian GAP-43 promoter in zebrafish
Development, January 7, 1994; 120(7): 1767 - 1775.
[Abstract] [PDF]



-

Home  |   Search  |   Archive  |   Subscribe  |   Contact  |   Help

-
Copyright 2008 by Society for Neuroscience ONLINE ISSN: 1529-2401
-