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J Neurochem ; 68(3): 1114-23, 1997 Mar.
Article in English | MEDLINE | ID: mdl-9048757

ABSTRACT

We have found that the early response of axotomized rat retinal ganglion cells is characterized by the differential regulation of a number of fast axonally transported proteins. The abundance of 23 radiolabeled fast transported proteins was analyzed at 2 and 5 days after axotomy using two-dimensional gel electrophoresis. Corresponding changes in retinal GAP-43 mRNA were measured using northern analysis. Within 2 days of injury, > 40% of the transported proteins analyzed, including GAP-43, showed increased labeling above control levels. Approximately 13% of transported proteins decreased below control levels, whereas the remainder did not change. Five days after axotomy, only GAP-43 and another fast transported protein, C3, continued to sustain measurable increased labeling above control levels; all previously elevated proteins appeared to have been down-regulated by this time, which corresponds to the onset of cell death. These differential changes were accompanied by parallel increases in GAP-43 mRNA. These results suggest that the molecular changes within rat retinal ganglion cells are differentially regulated within two stages subsequent to damage, initial regenerative growth followed by cell death.


Subject(s)
Axons/metabolism , Denervation , Nerve Tissue Proteins/metabolism , Retinal Ganglion Cells/metabolism , Animals , Female , Fluorometry , GAP-43 Protein , Male , Membrane Glycoproteins/genetics , Nerve Tissue Proteins/genetics , RNA, Messenger/metabolism , Rats , Rats, Sprague-Dawley , Time Factors
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