Regulation of EphB1 expression by dopamine signaling

被引:22
作者
Halladay, AK
Yue, Y
Michna, L
Widmer, DAJ
Wagner, GC
Zhou, R
机构
[1] Rutgers State Univ, Dept Psychol, Piscataway, NJ 08854 USA
[2] Rutgers State Univ, Dept Toxicol, Piscataway, NJ 08854 USA
[3] Rutgers State Univ, Canc Res Lab, Piscataway, NJ 08854 USA
来源
MOLECULAR BRAIN RESEARCH | 2000年 / 85卷 / 1-2期
关键词
dopamine; cocaine; nigrostriatal; cortex; development; receptor;
D O I
10.1016/S0169-328X(00)00249-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The Eph family tyrosine kinase receptors and their ligands have been implicated in axon guidance and neuronal migration during development of the nervous system. In the current study, we aim to characterize the nature of changes in EphB1 receptor expression following increases or decreases in dopamine activity. Neonatal mice (P3) were injected with 6-hydroxydopamine and allowed 13 days to recover. These animals show a profound depletion of dopamine in all areas assayed, with a corresponding dose-dependent decrease in EphB1 expression. Day 3 pups were also injected either chronically (P3-P16) or acutely (P3 only) with cocaine to determine how enhancing dopamine signaling would affect EphB1 signal density. It was found that both treatments significantly increased expression of EphB1 in the cortex, striatum and substantia nigra. Finally, animals were treated prenatally (E15-E17) with Cocaine and sacrificed on P7. These animals also showed an increase in EphB1 signal density, but only in the dopaminergic terminal areas in the cortex and striatum. These studies indicate that dopamine activity regulates developmental expression of the tyrosine kinase receptor EphB1. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:171 / 178
页数:8
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