ALTERED EXPRESSION OF PP60C-SRC INDUCED BY PERIPHERAL-NERVE INJURY

被引:20
作者
IGNELZI, MA
PADILLA, SS
WARDER, DE
MANESS, PF
机构
[1] UNIV N CAROLINA,SCH MED,DEPT BIOCHEM & BIOPHYS,CB 7260,505 FAC LAB OFF BLDG,CHAPEL HILL,NC 27599
[2] US EPA,DIV NEUROTOXICOL,CELLULAR & MOLEC TOXICOL BRANCH,RES TRIANGLE PK,NC 27711
关键词
PROTEIN TYROSINE KINASE; ONCOGENE; NERVE REGENERATION; CHICKENS;
D O I
10.1002/cne.903150205
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The normal src protein (pp60csrc) is localized principally in the nerve growth cone of developing neurons and declines to low levels with synaptic maturation. To determine whether pp60c-mrc is reexpressed in regenerating axons, its expression was studied by immunoblotting and immunocytochemical analyses in adult chicken sciatic nerve following nerve crush injury. pp60c-src expression was found to increase during nerve repair with a temporal and spatial pattern consistent with a localization in regenerating axons. At the crush site, pp60c-src: increased to maximal levels 7 days postinjury, increasing fivefold relative to 0 day nerve. In the nerve segment distal to the injury, the maximal increase in pp60c-src was sevenfold and occurred between 11 and 21 days postinjury. Immunoperoxidase staining revealed pp60c-src in regenerating axons and certain nonneuronal cells at the site of nerve repair. pp60csrc was induced in both motor and sensory neurons, as shown by increased pp60c-src immunoreactivity in their cell bodies located in the spinal cord and dorsal root ganglion. Phosphotyrosine-modified proteins that were potential targets of pp60c-mrc increased following nerve crush, and were localized to outgrowing neurites as well as to nonneuronal cells. These results suggest that pp60c-src is a common component of cellular mechanisms regulating growth cone migration in both regenerating and developing axons.
引用
收藏
页码:171 / 177
页数:7
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